Biodiversity is the feedstock for the biotechnology trade. Hence, the conservation, enhancement and sustainable and equitable use of biodiversity must be accorded excessive precedence in all nationwide atmosphere safety programmes. Lichens function helpful indicators of environmental well being. Similarly, a number of blue inexperienced algae assist to sequester salt from water.
There is want for the extra widespread use of such biomonitoring and bioremediation brokers. Bioprospecting analysis designed to establish novel metabolites have to be rooted within the precept of fairness in sharing advantages with the holders of conventional information.
There is want for better vigil against alien invasive species, since with rising world commerce in meals grains and different agricultural commodities, there may be an growing risk of introducing new pests, weeds and dangerous micro-organisms. Finally, organic scientists ought to place emphasis on their moral duty for the implications of their analysis, since in any other case bioterrorism may turn into a significant risk to human safety.
Net cost adjustments within the calculation of relative ligand-binding free energies by way of classical atomistic molecular dynamics simulation.
The calculation of binding free energies of charged species to a goal molecule is a often encountered drawback in molecular dynamics research of (bio-)chemical thermodynamics. Many necessary endogenous receptor-binding molecules, enzyme substrates, or drug molecules have a nonzero net cost. Absolute binding free energies, in addition to binding free energies relative to a different molecule with a distinct net cost can be affected by artifacts because of the used effective electrostatic interplay perform and related parameters (e.g., measurement of the computational field).
In the current research, charging contributions to binding free energies of small oligoatomic ions to a collection of mannequin host cavities functionalized with completely different chemical teams are calculated with classical atomistic molecular dynamics simulation. Electrostatic interactions are handled utilizing a lattice-summation scheme or a cutoff-truncation scheme with Barker-Watts reaction-field correction, and the simulations are carried out in containers of various edge lengths.
It is illustrated that the charging free energies of the visitor molecules in water and within the host strongly depend upon the utilized methodology and that neglect of correction phrases for the artifacts launched by the finite measurement of the simulated system and the usage of an effective electrostatic interplay perform significantly impairs the thermodynamic interpretation of guest-host interactions.
Application of correction phrases for the varied artifacts yields constant outcomes for the charging contribution to binding free energies and is thus a prerequisite for the legitimate interpretation or prediction of experimental information by way of molecular dynamics simulation. Analysis and correction of electrostatic artifacts based on the scheme proposed within the current research ought to subsequently be thought-about an integral a part of cautious free-energy calculation research if adjustments within the net cost are concerned.
Characterization of the purified Chlamydomonas minus agglutinin.
Chlamydomonas flagellar sexual agglutinins are liable for the adhesion of reverse mating-type (plus and minus) gametes in the course of the first phases of mating. Purification and partial characterization of the plus agglutinin was beforehand reported (Adair, W. S., C. J. Hwang, and U. W. Goodenough, 1983, Cell, 33:183-193). Here we characterize the purified minus molecule. We present it to be a excessive molecular weight, hydroxyproline-rich glycoprotein that migrates within the 3% stacking area of an SDS-polyacrylamide gel and is absent from two nonagglutinating minus mutants.
Plus and minus agglutinins are remarkably comparable, though nonidentical, in amino acid composition, molecular morphology, and reactivity in vivo and in vitro with monoclonal antibodies raised against the plus agglutinin. Moreover, the adhesiveness of each plus and minus agglutinins, when coupled to agarose beads, is abolished by thermolysin, trypsin, periodate, alkaline borohydride, lowering brokers, or warmth, however unaffected by exo- or endoglycosidases.
The minus agglutinin, nevertheless, migrates simply forward of the plus molecule on SDS PAGE, is excluded from an anion-exchange (Mono Q) column, elutes earlier throughout hydrophobic interplay (Bio-gel TSK Phenyl 5PW) chromatography, and is delicate to chymotrypsin digestion (in contrast to the plus agglutinin); subsequently, it differs from the plus agglutinin in obvious molecular weight, net cost, relative hydrophobicity and proteolytic susceptibility.
Nevertheless, our outcomes typically exhibit a excessive diploma of homology between these complementary cell-cell recognition/adhesion molecules, which means that they’re specified by genes which have a standard evolutionary origin.
The function of exonucleolytic processing and polymerase-DNA affiliation in bypass of lesions throughout replication in vitro. Significance for SOS-targeted mutagenesis.
The function of exonuclease exercise in trans-lesion DNA replication with Escherichia coli DNA polymerase III holoenzyme was investigated. RecA protein inhibited the three’—-5′ exonuclease exercise of the polymerase 2-fold when assayed within the absence of replication and had no impact on turnover of dNTPs into dNMPs. In distinction, single-stranded DNA-binding protein, which had no impact on the exonuclease exercise within the absence of replication, confirmed a pronounced 7-fold suppression of the three’—-5′ exonuclease exercise throughout replication.
The excision of integrated dNMP alpha S residues from DNA by the three’—-5′ exonuclease exercise of DNA polymerase III holoenzyme was inhibited 10-20-fold; nonetheless no enhance in bypass of pyrimidine photodimers was noticed. Thus, in settlement with our earlier outcomes during which the exonuclease exercise was inhibited on the protein stage (Livneh, Z. (1986) J. Biol. Chem. 261, 9526-9533), inhibition on the DNA stage additionally didn’t enhance bypass of photodimers.
Fractionation of the replication combination after termination of DNA synthesis on a Bio-Gel A-5m column underneath circumstances which favor polymerase-DNA binding yielded a termination advanced which may carry out turnover of dNTPs into dNMPs. Adding challenge-primed single-stranded DNA to the advanced yielded a burst of DNA synthesis which was promoted most definitely by DNA polymerase III holoenzyme molecules transferred from the termination advanced to the problem DNA thus demonstrating the instability of the polymerase-DNA affiliation.
Addition of a contemporary pattern of DNA polymerase III holoenzyme to purified termination merchandise, which consist primarily of partially replicated molecules with nascent chains terminated at UV lesions, didn’t lead to any net DNA synthesis as anticipated. However, reactivation of lesion-terminated primers was achieved by pretreatment with a 3′—-5′ exonuclease which excised 200 nucleotides or extra, producing new 3′-OH termini positioned away from the UV lesions.
75GPD RO MEMBRANE |
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| CDRC75201 | Scientific Laboratory Supplies | EACH | 1394.38 EUR |
Membrane Screw Cap |
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| BOT0112 | Scientific Laboratory Supplies | PK5 | 45.6 EUR |
Spoligotyping Membrane |
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| IM9702 | Mapmygenome | each | 1536 EUR |
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Description: A very simple, inexpensive and effective tool for Tuberculosis/ Mycobacterium research. Spoligotyping is a PCR-based Method to Simultaneously Detect and Type Mycobacterium Tuberculosis Complex Bacteria. Spoligotyping, which uses RLB (Reversed Line Blotting) offers an alternative for typical Southern blotting when rapid results are required. The method is particularly useful to simultaneously detect and type M. tuberculosis complex bacteria in clinical samples (suspected nosocomial infections, outbreaks in prisons, etc.). The level of differentiation by spoligotyping is less compared to IS6110 fingerprinting for strains having five or more IS6110 copies, but higher for strains with less than five copies. Thus, Spoligotyping is a preferred method to type M. bovis strains, which usually contain only one or two IS6110 copies. Note, that Mycobacterium bovis can be recognized by the absence of reactivity with spacers 39-43. |
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Filter Membrane 934Ah 90mm |
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| FIL4610 | Scientific Laboratory Supplies | PK100 | 147.6 EUR |
Filter Membrane 934Ah 110mm |
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| FIL4612 | Scientific Laboratory Supplies | PK100 | 202.8 EUR |
Membrane Filter Te37 |
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| 411205 | Scientific Laboratory Supplies | PK50 | 282 EUR |
A431 Membrane Lysate |
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| XBL-10438 | ProSci | 0.1 mg | 619.8 EUR |
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Description: A431 (Human Epidermoid Carcinoma) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The A431 (Human Epidermoid Carcinoma) cell was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated A431 (Human Epidermoid Carcinoma) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated A431 (Human Epidermoid Carcinoma) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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HeLa Membrane Lysate |
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| XBL-10439 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Hela (Human cervix Adenocarcinoma) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The Hela (Human cervix Adenocarcinoma) cell was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated Hela (cervix Adenocarcinoma) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated Hela (cervix Adenocarcinoma) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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K562 Membrane Lysate |
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| XBL-10441 | ProSci | 0.1 mg | 619.8 EUR |
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Description: K562 (Human Chronic Myelogenous Leukemia; Bone Marrow) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The K562 (Human Chronic Myelogenous Leukemia; Bone Marrow) cell was frozen in liquid nitrogen immediately after excision and then stored at -70ºC. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated K562 (Human Chronic Myelogenous Leukemia; Bone Marrow) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated K562 (Human Chronic Myelogenous Leukemia; Bone Marrow) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Raji Membrane Lysate |
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| XBL-10443 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Raji (Human lymphoma; B lymphoma) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The Raji (Human lymphoma; B lymphoma) cell was frozen in liquid nitrogen immediately after excision and then stored at -70ºC. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated Raji (Human lymphoma; B lymphoma) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated Raji (Human lymphoma; B lymphoma) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Lung Membrane Lysate |
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| XBL-10694 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human lung tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human lung tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated lung tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated lung tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Skin Membrane Lysate |
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| XBL-10864 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human skin tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human skin tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated skin tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated skin tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Brain Membrane Lysate |
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| 21-138 | ProSci | 0.1 mg | 682.8 EUR |
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Description: Monkey (Cynomolgus) brain tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The monkey (Cynomolgus) brain tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the brain tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
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Brain Membrane Lysate |
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| 21-241 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Monkey (Rhesus) brain tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The monkey (Rhesus) brain tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the brain tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
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Heart Membrane Lysate |
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| 21-243 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Monkey (Rhesus) heart tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The monkey (Rhesus) heart tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the heart tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated heart tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
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Brain Membrane Lysate |
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| 21-358 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Mouse brain tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The mouse brain tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the brain tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
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Brain Membrane Lysate |
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| 21-440 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Rat brain tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The rat brain tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the brain tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
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Zika Membrane Peptide |
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| 8667P | ProSci | 0.05 mg | 197.7 EUR |
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Description: Zika Membrane Peptide |
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Brain Membrane Lysate |
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| XBL-10166 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human brain tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human brain tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Colon Membrane Lysate |
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| XBL-10505 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human colon tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human colon tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated colon tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated colon tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Heart Membrane Lysate |
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| XBL-10595 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human heart tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human heart tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated heart tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated heart tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Liver Membrane Lysate |
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| XBL-10667 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human liver tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human liver tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated liver tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated liver tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Ovary Membrane Lysate |
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| XBL-10768 | ProSci | 0.1 mg | 991.5 EUR |
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Description: Human ovary tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human ovary tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated ovary tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated ovary tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Ileum Membrane Lysate |
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| XBL-10891 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human small intestine: Ileum tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human small intestine: Ileum tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated small intestine: Ileum tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated small intestine: Ileum tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Membrane Kit for 51302560 |
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| 51340293 | Scientific Laboratory Supplies | EACH | 261.6 EUR |
TMB Membrane Substrate |
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| 42-TB07 | Fitzgerald | 100 ml | 158.4 EUR |
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Description: High sensitivity HRP membrane substrate (containing TMB) |
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Zika Membrane Antibody |
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| 8667-002mg | ProSci | 0.02 mg | 206.18 EUR |
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Description: Zika virus (ZIKV) is a member of the virus family Flaviviridae. It is spread by daytime-active Aedes mosquitoes, such as A. aegypti and A. albopictus. Zika virus is related to the dengue, yellow fever, Japanese encephalitis, and West Nile viruses. Zika often causes no or only mild symptoms, similar to a very mild form of dengue fever. Zika can also spread from a pregnant woman to her fetus. This can result in microcephaly, severe brain malformations, and other birth defects. This antibody is specific to the Membrane protein. |
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Zika Membrane Antibody |
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| 8667-01mg | ProSci | 0.1 mg | 523.7 EUR |
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Description: Zika virus (ZIKV) is a member of the virus family Flaviviridae. It is spread by daytime-active Aedes mosquitoes, such as A. aegypti and A. albopictus. Zika virus is related to the dengue, yellow fever, Japanese encephalitis, and West Nile viruses. Zika often causes no or only mild symptoms, similar to a very mild form of dengue fever. Zika can also spread from a pregnant woman to her fetus. This can result in microcephaly, severe brain malformations, and other birth defects. This antibody is specific to the Membrane protein. |
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Nylon Membrane (30cmx3m) |
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| D0157-3 | Bio Basic | 1(30cmx3m), 1 UNIT | 1043.1 EUR |
Dialysis membrane, 34mm |
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| TX0111 | Bio Basic | 2m, 2m | 78.79 EUR |
Dialysis membrane, 44mm |
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| TX0112 | Bio Basic | 2m, 2m | 82.97 EUR |
Dialysis membrane, 77mm |
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| TX0113 | Bio Basic | 2m, 2m | 93.41 EUR |
Jurkat Membrane Lysate |
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| XBL-10440 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Jurkat (Human Acute T cell Leukemia) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The Jurkat (Human Acute T cell Leukemia) cell was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated Jurkat (Human Acute T cell Leukemia) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated Jurkat (Human Acute T cell Leukemia) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Artery Membrane Lysate |
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| XBL-10484 | ProSci | 0.1 mg | 884.4 EUR |
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Description: Human blood vessel: artery tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human blood vessel: artery tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated blood vessel: artery tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated blood vessel: artery tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Breast Membrane Lysate |
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| XBL-10496 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human breast tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human breast tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated breast tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated breast tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Kidney Membrane Lysate |
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| XBL-10649 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human kidney tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human kidney tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated kidney tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated kidney tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Rectum Membrane Lysate |
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| XBL-10834 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human rectum tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human rectum tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated rectum tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated rectum tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Spleen Membrane Lysate |
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| XBL-10909 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human spleen tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human spleen tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated spleen tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated spleen tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Testis Membrane Lysate |
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| XBL-10957 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human testis tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human testis tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated testis tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated testis tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Thymus Membrane Lysate |
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| XBL-10978 | ProSci | 0.1 mg | 991.5 EUR |
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Description: Human thymus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human thymus tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated thymus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated thymus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Tonsil Membrane Lysate |
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| XBL-11004 | ProSci | 0.1 mg | 884.4 EUR |
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Description: Human tonsil tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human tonsil tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated tonsil tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated tonsil tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Uterus Membrane Lysate |
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| XBL-11023 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human uterus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human uterus tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated uterus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated uterus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Vagina Membrane Lysate |
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| XBL-11043 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human vagina tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human vagina tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated vagina tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated vagina tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Filter Membrane 934 Ah 70mm |
|||
| FIL4608 | Scientific Laboratory Supplies | PK100 | 109.2 EUR |
Adipose Membrane Lysate |
|||
| XBL-10451 | ProSci | 0.1 mg | 884.4 EUR |
|
Description: Human adipose tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human adipose tissue was frozen in liquid nitrogen immediately after excision and then stored at -70ºC. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated adipose tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated adipose tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Adrenal Membrane Lysate |
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| XBL-10454 | ProSci | 0.1 mg | 884.4 EUR |
|
Description: Human adrenal tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human adrenal tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated adrenal tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated adrenal tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Bladder Membrane Lysate |
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| XBL-10475 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human bladder tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human bladder tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated bladder tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated bladder tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Trachea Membrane Lysate |
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| XBL-10727 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human lung trachea tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human lung trachea tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated lung trachea tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated lung trachea tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Jejunum Membrane Lysate |
|||
| XBL-10900 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human small intestine: Jejunum tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human small intestine: Jejunum tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated small intestine: Jejunum tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated small intestine: Jejunum tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Stomach Membrane Lysate |
|||
| XBL-10924 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human stomach tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human stomach tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated stomach tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated stomach tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Thyroid Membrane Lysate |
|||
| XBL-10987 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human thyroid tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human thyroid tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated thyroid tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated thyroid tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Membrane Holder St St |
|||
| 1980-001 | Scientific Laboratory Supplies | EACH | 190.8 EUR |
PM2.5 Membrane PTFE 46.2mm |
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| 7592-104 | Scientific Laboratory Supplies | PK50 | 558 EUR |
85mm 0.45um CN Membrane |
|||
| FIL1312 | Scientific Laboratory Supplies | PK100 | 568.8 EUR |
Thalamus Membrane Lysate |
|||
| XBL-10204 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human brain thalamus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human thalamus tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain thalamus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain thalamus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Amygdala Membrane Lysate |
|||
| XBL-10237 | ProSci | 0.1 mg | 884.4 EUR |
|
Description: Human brain amygdala tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human amygdala tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain amygdala tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain amygdala tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Duodenum Membrane Lysate |
|||
| XBL-10547 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human duodenum tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human duodenum tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated duodenum tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated duodenum tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Pancreas Membrane Lysate |
|||
| XBL-10780 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human pancreas tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human pancreas tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated pancreas tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated pancreas tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Placenta Membrane Lysate |
|||
| XBL-10819 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human placenta tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human placenta tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated placenta tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated placenta tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Prostate Membrane Lysate |
|||
| XBL-10822 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human prostate tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human prostate tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated prostate tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated prostate tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Filter Membrane 934-Ah 24mm |
|||
| FIL4600 | Scientific Laboratory Supplies | PK100 | 31.2 EUR |
Filter Membrane 934-Ah 47mm |
|||
| FIL4604 | Scientific Laboratory Supplies | PK100 | 79.2 EUR |
MCF 7 Membrane Lysate |
|||
| XBL-10442 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: MCF 7 (Human breast Adenocarcinima) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The MCF 7 (Human breast Adenocarcinima) cell was frozen in liquid nitrogen immediately after excision and then stored at -70ºC. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated MCF 7 (Human breast Adenocarcinima) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated MCF 7 (Human breast Adenocarcinima) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Membrane Filter Dispenser |
|||
| FIL1008 | Scientific Laboratory Supplies | EACH | 2114.4 EUR |
Pituitary Membrane Lysate |
|||
| XBL-10263 | ProSci | 0.1 mg | 1186.8 EUR |
|
Description: Human brain pituitary tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human pituitary tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain pituitary tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain pituitary tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Diaphragm Membrane Lysate |
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| XBL-10535 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human diaphragm tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human diaphragm tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated diaphragm tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated diaphragm tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Esophagus Membrane Lysate |
|||
| XBL-10565 | ProSci | 0.1 mg | 619.8 EUR |
|
Description: Human esophagus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human esophagus tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated esophagus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated esophagus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Epididymus Membrane Lysate |
|||
| XBL-10562 | ProSci | 0.1 mg | 884.4 EUR |
|
Description: Human Epididymus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human Epididymus tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated Epididymus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated Epididymus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Filter Membrane 3Um 47mm |
|||
| 7193-004 | Scientific Laboratory Supplies | PK100 | 222 EUR |
CN Membrane 0.45um sterile |
|||
| FIL1250 | Scientific Laboratory Supplies | PK48 | 178.8 EUR |
Hippocampus Membrane Lysate |
|||
| XBL-10180 | ProSci | 0.1 mg | 1023 EUR |
|
Description: Human brain hippocamps tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human hippocamps tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain hippocamps tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain hippocamps tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Gallbladder Membrane Lysate |
|||
| XBL-10583 | ProSci | 0.1 mg | 884.4 EUR |
|
Description: Human gallbladder tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human gallbladder tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated gallbladder tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated gallbladder tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Parathyroid Membrane Lysate |
|||
| XBL-10798 | ProSci | 0.1 mg | 1186.8 EUR |
|
Description: Human parathyroid tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human parathyroid tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated parathyroid tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated parathyroid tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Nitrocellulose Membrane Roll |
|||
| B500 | ABM | 3m x 30cm Roll | 326.4 EUR |
Nitrocellulose Membrane 0.22um |
|||
| NT020S1 | Bio Basic | 5(20x20cm), 5UNIT | 151.87 EUR |
Vivaspin 500 PES Membrane 3000Da MWCO |
|||
| FIL8546 | Scientific Laboratory Supplies | PK25 | 157.2 EUR |
Vivaspin 500 PES Membrane 3000Da MWCO |
|||
| FIL8548 | Scientific Laboratory Supplies | PK100 | 514.8 EUR |
Vivaspin 500 PES Membrane 30000Da MWCO |
|||
| FIL8569 | Scientific Laboratory Supplies | PK25 | 158.4 EUR |
Vivaspin 500 PES Membrane 300000Da MWCO |
|||
| FIL8571 | Scientific Laboratory Supplies | PK100 | 514.8 EUR |
Vivaspin 500 PES Membrane 1000000Da MWCO |
|||
| FIL8573 | Scientific Laboratory Supplies | PK25 | 157.2 EUR |
Vivaspin 500 PES Membrane 1000000Da MWCO |
|||
| FIL8575 | Scientific Laboratory Supplies | PK100 | 514.8 EUR |
Vivaspin 2 PES Membrane 3000Da MWCO |
|||
| FIL8597 | Scientific Laboratory Supplies | PK25 | 204 EUR |
Vivaspin 2 PES Membrane 3000Da MWCO |
|||
| FIL8599 | Scientific Laboratory Supplies | PK100 | 675.6 EUR |
Vivaspin 20 PES Membrane 3000Da MWCO |
|||
| FIL8617 | Scientific Laboratory Supplies | PK12 | 218.4 EUR |
Vivaspin 2 PES Membrane 300000Da MWCO |
|||
| FIL8621 | Scientific Laboratory Supplies | PK100 | 675.6 EUR |
Vivaspin 2 PES Membrane 1000000Da MWCO |
|||
| FIL8623 | Scientific Laboratory Supplies | PK25 | 204 EUR |
Vivaspin 2 PES Membrane 1000000Da MWCO |
|||
| FIL8625 | Scientific Laboratory Supplies | PK100 | 675.6 EUR |
Bone Membrane Tumor Lysate |
|||
| XBL-10493 | ProSci | 0.1 mg | 1023 EUR |
|
Description: Human bone tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human bone tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated bone tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated bone tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Lung Membrane Tumor Lysate |
|||
| XBL-10709 | ProSci | 0.1 mg | 752.1 EUR |
|
Description: Human lung tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human lung tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated lung tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated lung tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Lymph node Membrane Lysate |
|||
| XBL-10732 | ProSci | 0.1 mg | 884.4 EUR |
|
Description: Human lymph node tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human lymph node tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated lymph node tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated lymph node tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Skin Membrane Tumor Lysate |
|||
| XBL-10873 | ProSci | 0.1 mg | 752.1 EUR |
|
Description: Human skin tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human skin tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated skin tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated skin tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Nitrocellulose Membrane Precut |
|||
| B501 | ABM | Pack of 30, 6cm x 8.5cm | 148.8 EUR |
Nuclepore pc membrane black |
|||
| 110656 | Scientific Laboratory Supplies | PK100 | 138 EUR |
Sartorius Membrane MGB 150mm |
|||
| SAR4226 | Scientific Laboratory Supplies | PK50 | 210 EUR |
Sartorius Membrane MGB 240mm |
|||
| SAR4231 | Scientific Laboratory Supplies | PK25 | 178.8 EUR |
Sartorius Membrane MGC 25mm |
|||
| SAR4304 | Scientific Laboratory Supplies | PK100 | 40.8 EUR |
Sartorius Membrane MGC 47mm |
|||
| SAR4310 | Scientific Laboratory Supplies | PK100 | 60 EUR |
Sartorius Membrane MGC 50mm |
|||
| SAR4311 | Scientific Laboratory Supplies | PK100 | 68.4 EUR |
Sartorius Membrane MGC 55mm |
|||
| SAR4312 | Scientific Laboratory Supplies | PK100 | 69.6 EUR |
Sartorius Membrane MGC 70mm |
|||
| SAR4314 | Scientific Laboratory Supplies | PK100 | 75.6 EUR |
Sartorius Membrane MGC 90mm |
|||
| SAR4316 | Scientific Laboratory Supplies | PK100 | 118.8 EUR |
Sartorius Membrane MGC 100mm |
|||
| SAR4317 | Scientific Laboratory Supplies | PK100 | 135.6 EUR |
Sartorius Membrane MGC 110mm |
|||
| SAR4318 | Scientific Laboratory Supplies | PK100 | 154.8 EUR |
Sartorius Membrane MGD 25mm |
|||
| SAR4408 | Scientific Laboratory Supplies | PK50 | 24 EUR |
Sartorius Membrane MGD 47mm |
|||
| SAR4414 | Scientific Laboratory Supplies | PK50 | 31.2 EUR |
Sartorius Membrane MGD 70mm |
|||
| SAR4418 | Scientific Laboratory Supplies | PK50 | 50.4 EUR |
Sartorius Membrane MGD 90mm |
|||
| SAR4420 | Scientific Laboratory Supplies | PK50 | 80.4 EUR |
Sartorius Membrane MGD 100mm |
|||
| SAR4421 | Scientific Laboratory Supplies | PK50 | 93.6 EUR |
Sartorius Membrane MGD 125mm |
|||
| SAR4424 | Scientific Laboratory Supplies | PK50 | 135.6 EUR |
Sartorius Membrane MGE 25mm |
|||
| SAR4504 | Scientific Laboratory Supplies | PK100 | 91.2 EUR |
Sartorius Membrane MGE 47mm |
|||
| SAR4510 | Scientific Laboratory Supplies | PK100 | 152.4 EUR |
Sartorius Membrane MGE 55mm |
|||
| SAR4512 | Scientific Laboratory Supplies | PK100 | 169.2 EUR |
Sartorius Membrane MGE 90mm |
|||
| SAR4516 | Scientific Laboratory Supplies | PK25 | 296.4 EUR |
Sartorius Membrane MGE 110mm |
|||
| SAR4518 | Scientific Laboratory Supplies | PK25 | 378 EUR |
Sartorius Membrane MGE 125mm |
|||
| SAR4520 | Scientific Laboratory Supplies | PK25 | 501.6 EUR |
Sartorius Membrane MGE 150mm |
|||
| SAR4522 | Scientific Laboratory Supplies | PK100 | 718.8 EUR |
Sartorius Membrane MGA 47mm |
|||
| SAR4112 | Scientific Laboratory Supplies | PK100 | 56.4 EUR |
Sartorius Membrane MGA 50mm |
|||
| SAR4114 | Scientific Laboratory Supplies | PK100 | 51.6 EUR |
Sartorius Membrane MGA 55mm |
|||
| SAR4116 | Scientific Laboratory Supplies | PK100 | 51.6 EUR |
Sartorius Membrane MGA 70mm |
|||
| SAR4120 | Scientific Laboratory Supplies | PK100 | 72 EUR |
Sartorius Membrane MGA 90mm |
|||
| SAR4122 | Scientific Laboratory Supplies | PK100 | 91.2 EUR |
Sartorius Membrane MGA 110mm |
|||
| SAR4124 | Scientific Laboratory Supplies | PK100 | 121.2 EUR |
Sartorius Membrane MGA 125mm |
|||
| SAR4126 | Scientific Laboratory Supplies | PK100 | 136.8 EUR |
Sartorius Membrane MGA 150mm |
|||
| SAR4128 | Scientific Laboratory Supplies | PK100 | 169.2 EUR |
Sartorius Membrane MGB 25mm |
|||
| SAR4204 | Scientific Laboratory Supplies | PK50 | 27.6 EUR |
Sartorius Membrane MGB 47mm |
|||
| SAR4210 | Scientific Laboratory Supplies | PK50 | 49.2 EUR |
Sartorius Membrane MGB 50mm |
|||
| SAR4211 | Scientific Laboratory Supplies | PK50 | 49.2 EUR |
Sartorius Membrane MGB 55mm |
|||
| SAR4212 | Scientific Laboratory Supplies | PK50 | 56.4 EUR |
Sartorius Membrane MGB 70mm |
|||
| SAR4216 | Scientific Laboratory Supplies | PK50 | 76.8 EUR |
Sartorius Membrane MGB 90mm |
|||
| SAR4218 | Scientific Laboratory Supplies | PK50 | 97.2 EUR |
Sartorius Membrane MGB 100mm |
|||
| SAR4219 | Scientific Laboratory Supplies | PK50 | 111.6 EUR |
Sartorius Membrane MGB 110mm |
|||
| SAR4220 | Scientific Laboratory Supplies | PK50 | 124.8 EUR |
Sartorius Membrane MGB 125mm |
|||
| SAR4222 | Scientific Laboratory Supplies | PK50 | 136.8 EUR |
Spinal cord Membrane Lysate |
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| XBL-10233 | ProSci | 0.1 mg | 884.4 EUR |
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Description: Human spinal cord tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human spinal cord tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated spinal cord tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated spinal cord tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Brain Membrane Tumor Lysate |
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| XBL-10257 | ProSci | 0.1 mg | 1023 EUR |
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Description: Human brain tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human brain tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Colon Membrane Tumor Lysate |
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| XBL-10520 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human colon tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human colon tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated colon tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated colon tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Liver Membrane Tumor Lysate |
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| XBL-10679 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human liver tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human liver tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated liver tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated liver tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Ovary Membrane Tumor Lysate |
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| XBL-10777 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human ovary tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human ovary tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated ovary tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated ovary tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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WHATMAN OE67 MEMBRANE 0.455m110MM DIAM |
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| WHA10404026 | Scientific Laboratory Supplies | EACH | 476.4 EUR |
Purite Ultrafiltration Membrane |
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| R090142 | Scientific Laboratory Supplies | EACH | 284.4 EUR |
Frontal Lobe Membrane Lysate |
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| XBL-10176 | ProSci | 0.1 mg | 619.8 EUR |
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Description: Human brain frontal lobe tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human frontal lobe tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain frontal lobe tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain frontal lobe tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Breast Membrane Tumor Lysate |
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| XBL-10499 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human breast tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human breast tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated breast tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated breast tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Kidney Membrane Tumor Lysate |
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| XBL-10661 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human kidney tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human kidney tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated kidney tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated kidney tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Rectum Membrane Tumor Lysate |
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| XBL-10843 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human rectum tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human rectum tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated rectum tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated rectum tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Spleen Membrane Tumor Lysate |
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| XBL-10921 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human spleen tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human spleen tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated spleen tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated spleen tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Testis Membrane Tumor Lysate |
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| XBL-10966 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human testis tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human testis tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated testis tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated testis tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Thymus Membrane Tumor Lysate |
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| XBL-10984 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human thymus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human thymus tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated thymus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated thymus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Tonsil Membrane Tumor Lysate |
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| XBL-11009 | ProSci | 0.1 mg | 1023 EUR |
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Description: Human tonsil tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human tonsil tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated tonsil tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated tonsil tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Ureter Membrane Tumor Lysate |
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| XBL-11020 | ProSci | 0.1 mg | 1023 EUR |
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Description: Human ureter tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human ureter tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated ureter tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated ureter tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Uterus Membrane Tumor Lysate |
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| XBL-11031 | ProSci | 0.1 mg | 752.1 EUR |
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Description: Human uterus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human uterus tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated uterus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated uterus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
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Pig Membrane IgA ELISA kit |
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| E07M0284-192T | BlueGene | 192 tests | 1524 EUR |
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Description: A competitive ELISA for quantitative measurement of Porcine Membrane IgA in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Pig Membrane IgA ELISA kit |
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| E07M0284-48 | BlueGene | 1 plate of 48 wells | 624 EUR |
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Description: A competitive ELISA for quantitative measurement of Porcine Membrane IgA in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Pig Membrane IgA ELISA kit |
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| E07M0284-96 | BlueGene | 1 plate of 96 wells | 822 EUR |
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Description: A competitive ELISA for quantitative measurement of Porcine Membrane IgA in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Pig Membrane IgM ELISA kit |
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| E07M0351-192T | BlueGene | 192 tests | 1524 EUR |
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Description: A competitive ELISA for quantitative measurement of Porcine Membrane IgM in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Pig Membrane IgM ELISA kit |
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| E07M0351-48 | BlueGene | 1 plate of 48 wells | 624 EUR |
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Description: A competitive ELISA for quantitative measurement of Porcine Membrane IgM in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Pig Membrane IgM ELISA kit |
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| E07M0351-96 | BlueGene | 1 plate of 96 wells | 822 EUR |
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Description: A competitive ELISA for quantitative measurement of Porcine Membrane IgM in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Dog Membrane IgA ELISA kit |
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| E08M0284-192T | BlueGene | 192 tests | 1524 EUR |
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Description: A competitive ELISA for quantitative measurement of Canine Membrane IgA in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Dog Membrane IgA ELISA kit |
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| E08M0284-48 | BlueGene | 1 plate of 48 wells | 624 EUR |
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Description: A competitive ELISA for quantitative measurement of Canine Membrane IgA in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Dog Membrane IgA ELISA kit |
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| E08M0284-96 | BlueGene | 1 plate of 96 wells | 822 EUR |
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Description: A competitive ELISA for quantitative measurement of Canine Membrane IgA in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Dog Membrane IgM ELISA kit |
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| E08M0351-192T | BlueGene | 192 tests | 1524 EUR |
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Description: A competitive ELISA for quantitative measurement of Canine Membrane IgM in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Dog Membrane IgM ELISA kit |
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| E08M0351-48 | BlueGene | 1 plate of 48 wells | 624 EUR |
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Description: A competitive ELISA for quantitative measurement of Canine Membrane IgM in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Dog Membrane IgM ELISA kit |
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| E08M0351-96 | BlueGene | 1 plate of 96 wells | 822 EUR |
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Description: A competitive ELISA for quantitative measurement of Canine Membrane IgM in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Rat Membrane IgA ELISA kit |
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| E02M0284-192T | BlueGene | 192 tests | 1524 EUR |
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Description: A competitive ELISA for quantitative measurement of Rat Membrane IgA in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Rat Membrane IgA ELISA kit |
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| E02M0284-48 | BlueGene | 1 plate of 48 wells | 624 EUR |
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Description: A competitive ELISA for quantitative measurement of Rat Membrane IgA in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Rat Membrane IgA ELISA kit |
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| E02M0284-96 | BlueGene | 1 plate of 96 wells | 822 EUR |
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Description: A competitive ELISA for quantitative measurement of Rat Membrane IgA in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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Rat Membrane IgM ELISA kit |
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| E02M0351-192T | BlueGene | 192 tests | 1524 EUR |
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Description: A competitive ELISA for quantitative measurement of Rat Membrane IgM in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species. |
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When these exonuclease-treated merchandise have been subjected to a second spherical of replication, an elevated stage of DNA synthesis was noticed together with extra bypass of photodimers. These outcomes recommend the likelihood that 3′—-5′ exonuclease processing may be required not less than transiently throughout one of many phases of trans-lesion DNA replication, which is believed to be the mechanism of SOS-targeted mutagenesis.