Biocat Net

Amine biocat 3.0

Bio-diversity: an effective safety net against environmental pollution.

Bio-diversity: an effective safety net against environmental pollution.
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.
Bio-diversity: an effective safety net against environmental pollution.
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.

Antigen-Antibody Pen For Human Primary antibodies

PEN-H7 1
EUR 202

Antigen-Antibody Pen For Mouse Primary antibodies

PEN-M2 1
EUR 202

Antigen-Antibody Pen For Rabbit Primary antibodies

PEN-R1 1
EUR 202

Antigen-Antibody Pen For Rat Primary antibodies

PEN-R10 1
EUR 202

Antigen-Antibody Pen For Sheep Primary antibodies

PEN-S4 1
EUR 202

Antigen-Antibody Pen For Hamster Primary antibodies

PEN-T8 1
EUR 202

Antigen-Antibody Pen For G. Pig Primary antibodies

PEN-P6 1
EUR 202

Antigen-Antibody Pen For Biotin-tagged antibodies (all species)

PEN-B9 1
EUR 202

Pen m2

LF-P0523 0.1 mg
EUR 350
Description: Pen m2 protein

Pen m2

LF-P0523A 0.5 mg
EUR 1247
Description: Pen m2 protein

Pen m2

LF-P0523B 1 mg
EUR 1998
Description: Pen m2 protein

PAP Pen

LP0001 1 ea.
EUR 156

H-Pen-OH

F-2515.0005 5.0g
EUR 151
Description: Sum Formula: C5H11NO2S; CAS# [1113-41-3]

H-Pen-OH

F-2515.0025 25.0g
EUR 490
Description: Sum Formula: C5H11NO2S; CAS# [1113-41-3]

PAP Pen-Mini

LP0002 1 ea.
EUR 120

Fmoc-Pen(Acm)-OH

B-1885.0001 1.0g
EUR 273
Description: Sum Formula: C23H26N2O5S; CAS# [201531-76-2]

Fmoc-Pen(Acm)-OH

B-1885.0005 5.0g
EUR 998
Description: Sum Formula: C23H26N2O5S; CAS# [201531-76-2]

Fmoc-Pen(Trt)-OH

B-2315.0001 1.0g
EUR 284
Description: Sum Formula: C39H35NO4S; CAS# [201531-88-6]

Fmoc-Pen(Trt)-OH

B-2315.0005 5.0g
EUR 1046
Description: Sum Formula: C39H35NO4S; CAS# [201531-88-6]

Fmoc-Pen(Trt)-OH

B-2315.0025 25.0g
EUR 4093
Description: Sum Formula: C39H35NO4S; CAS# [201531-88-6]

H-D-Pen-OH

F-4235.0005 5.0g
EUR 151
Description: Sum Formula: C5H11NO2S; CAS# [52-67-5]

H-D-Pen-OH

F-4235.0025 25.0g
EUR 515
Description: Sum Formula: C5H11NO2S; CAS# [52-67-5]

Boc-Pen(NPys)-OH

A-3650.0001 1.0g
EUR 381
Description: Sum Formula: C15H21N3O6S2; CAS# [250375-03-2]

Boc-Pen(NPys)-OH

A-3650.0005 5.0g
EUR 1421
Description: Sum Formula: C15H21N3O6S2; CAS# [250375-03-2]

Boc-Pen(Mob)-OH

A-2900.0001 1.0g
EUR 151
Description: Sum Formula: C18H27NO5S; CAS# [120944-75-4]

Boc-Pen(Mob)-OH

A-2900.0005 5.0g
EUR 526
Description: Sum Formula: C18H27NO5S; CAS# [120944-75-4]

Boc-Pen(Trt)-OH

A-3550.0001 1.0g
EUR 309
Description: Sum Formula: C29H33NO4S; CAS# [135592-13-1]

Boc-Pen(Trt)-OH

A-3550.0005 5.0g
EUR 1143
Description: Sum Formula: C29H33NO4S; CAS# [135592-13-1]

Boc-Pen(pMeBzl)-OH.DCHA

A6663-1000 1 g
EUR 427
Description: Boc-Pen(pMeBzl)-OH.DCHA

Boc-Pen(pMeBzl)-OH.DCHA

A6663-5000 5 g
EUR 1407
Description: Boc-Pen(pMeBzl)-OH.DCHA

Boc-Pen(pMeBzl)-OH

5-05183 5g Ask for price

Boc-Pen(pMeBzl)-OH

5-05184 25g Ask for price

Fmoc-Pen(Acm)-OH

5-05185 1g Ask for price

Fmoc-Pen(Acm)-OH

5-05186 5g Ask for price

Boc-Pen(Trt)-OH

5-05187 1g Ask for price

Boc-Pen(Trt)-OH

5-05188 5g Ask for price

Fmoc-Pen(Trt)-OH

5-05189 1g Ask for price

Fmoc-Pen(Trt)-OH

5-05190 5g Ask for price

Super HT PAP Pen

22006 1EA
EUR 181
Description: Minimum order quantity: 1 unit of 1EA

WB 4101 hydrochloride

B6515-25 25 mg
EUR 242

WB Stripping Buffer

AR0153 100mL (for 10 assays for an 5 × 8.5cm blot)
EUR 111

HPSE-WB Recombinant Protein Human Heparanase-1 WB Control

PROTQ9Y251 Regular: 200ng
EUR 1104
Description: Recombinant Heparanase protein HPA1 is produced in CHO cells.;The protein is purified by several orthogonal chromatography steps.

Fmoc-D-Pen(Acm)-OH

B-1915.0001 1.0g
EUR 273
Description: Sum Formula: C23H26N2O5S; CAS# [201531-77-3]

Fmoc-D-Pen(Acm)-OH

B-1915.0005 5.0g
EUR 998
Description: Sum Formula: C23H26N2O5S; CAS# [201531-77-3]

Fmoc-D-Pen(Trt)-OH

B-2320.0001 1.0g
EUR 284
Description: Sum Formula: C39H35NO4S; CAS# [201532-01-6]

Fmoc-D-Pen(Trt)-OH

B-2320.0005 5.0g
EUR 1046
Description: Sum Formula: C39H35NO4S; CAS# [201532-01-6]

Fmoc-D-Pen(Trt)-OH

B-2320.0025 25.0g
EUR 4093
Description: Sum Formula: C39H35NO4S; CAS# [201532-01-6]

H-D-Pen(Trt)-OH

F-3070.0001 1.0g
EUR 309
Description: Sum Formula: C24H25NO2S; CAS# [150025-01-7]

H-D-Pen(Trt)-OH

F-3070.0005 5.0g
EUR 1143
Description: Sum Formula: C24H25NO2S; CAS# [150025-01-7]

Boc-D-Pen(NPys)-OH

A-3655.0001 1.0g
EUR 381
Description: Sum Formula: C15H21N3O6S2; CAS# [153815-23-7]

Boc-D-Pen(NPys)-OH

A-3655.0005 5.0g
EUR 1421
Description: Sum Formula: C15H21N3O6S2; CAS# [153815-23-7]

Boc-D-Pen(Trt)-OH

A-3555.0001 1.0g
EUR 170
Description: Sum Formula: C29H33NO4S; CAS# [135592-14-2]

Boc-D-Pen(Trt)-OH

A-3555.0005 5.0g
EUR 587
Description: Sum Formula: C29H33NO4S; CAS# [135592-14-2]

Boc-D-Pen(Acm)-OH

5-05193 5g Ask for price

Boc-D-Pen(Acm)-OH

5-05194 25g Ask for price

Boc-D-Pen(Trt)-OH

5-05197 5g Ask for price

Boc-D-Pen(Trt)-OH

5-05198 10g Ask for price

Fmoc-D-Pen(Acm)-OH

5-05199 1g Ask for price

Fmoc-D-Pen(Acm)-OH

5-05200 5g Ask for price

Fmoc-D-Pen(Trt)-OH

5-05201 10g Ask for price

Fmoc-D-Pen(Trt)-OH

5-05202 50g Ask for price

Ac-DL-Pen(Acm)-OH

5-05203 5g Ask for price

Ac-DL-Pen(Acm)-OH

5-05204 25g Ask for price

Mini Super HT PAP Pen

22005 1EA
EUR 143
Description: Minimum order quantity: 1 unit of 1EA

Human Penguin(PEN)ELISA Kit

QY-E04702 96T
EUR 361

WB Developing Fixing Kit

AR0132 1kit (Enough for 10 assays)
EUR 75

CHO HCP WB kit

F060 1 kit (application dependant amount of reactions)
EUR 836
  • Product category: Premade blotting kit
Description: CHO HCP WB kit by Cygnus Technologies is available in Europe via Gentaur.

S.cerevisiae HCP WB kit

F130 1 kit (application dependant amount of reactions)
EUR 836
  • Product category: Premade blotting kit
Description: S.cerevisiae HCP WB kit by Cygnus Technologies is available in Europe via Gentaur.

A549 HCP WB kit

F235 1 kit (application dependant amount of reactions)
EUR 836
  • Product category: Premade blotting kit
Description: A549 HCP WB kit by Cygnus Technologies is available in Europe via Gentaur.

E.coli HCP WB kit

F415 1 kit (application dependant amount of reactions)
EUR 836
  • Product category: Premade blotting kit
Description: E.coli HCP WB kit by Cygnus Technologies is available in Europe via Gentaur.

WB / Antibody Stripping Buffer

20-abx090656
  • EUR 189.00
  • EUR 230.00
  • 100 ml
  • 200 ml
  • Shipped within 5-10 working days.

WB / Antibody Stripping Buffer

abx090671-200ml 200 ml
EUR 189
  • Shipped within 5-10 working days.

101Bio WB Stripping Solution

P5W3 NULL
EUR 0

101Bio WB Blocking Solution

P5W8 NULL
EUR 0

Topoisomerase I WB Marker

TG2011-4 20 units
EUR 436

Block

H5000-WB 1 PC
EUR 4288.85
  • To order instruments in 115V / US plug please delete the 'E' off the order code.European 2 pin plugs will be supplied as standard, please request UK if required.

Wash buffer concentrate (100X) for ELISA, 10 ml

WB-100 10 ml
EUR 103

Wash buffer concentrate (100X) for ELISA

WB-150 50 ml
EUR 116

Pichia pastoris HCP WB kit

F145 1 kit (application dependant amount of reactions)
EUR 836
  • Product category: Premade blotting kit
Description: Pichia pastoris HCP WB kit by Cygnus Technologies is available in Europe via Gentaur.

SP2/0 HCP WB kit

F185 1 kit (application dependant amount of reactions)
EUR 836
  • Product category: Premade blotting kit
Description: SP2/0 HCP WB kit by Cygnus Technologies is available in Europe via Gentaur.

NS/0 HCP WB kit

F225 1 kit (application dependant amount of reactions)
EUR 836
  • Product category: Premade blotting kit
Description: NS/0 HCP WB kit by Cygnus Technologies is available in Europe via Gentaur.

WB Developing and Fixing Kit

20-abx090662
  • EUR 189.00
  • EUR 230.00
  • 100 ml
  • 500 ml
  • Shipped within 5-10 working days.

WB Developing and Fixing Kit

abx090672-500ml 500 ml
EUR 189
  • Shipped within 5-10 working days.

TrueBlack WB Blocking Buffer Kit

23013 1kit
EUR 347
Description: Minimum order quantity: 1 unit of 1kit

TrueBlack WB Blocking Buffer Kit

23013-T 1kit
EUR 125
Description: Minimum order quantity: 1 unit of 1kit

CHO-CM HCP WB kit

CM060 1 kit (application dependant amount of reactions)
EUR 792
  • Product category: Premade blotting kit
Description: CHO-CM HCP WB kit by Cygnus Technologies is available in Europe via Gentaur.

WB ECM kit (Mouse IgG)

LF-QC5001 1 kit
EUR 253
Description: Our Enhanced Chemiluminescent Kit is an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Powered by our proprietary and easy to use substrates, a unique blocking agent, highly specific secondary antibodies, and carefully optimized protocols, this kit offers the highest signal to noise ratio available and yields clean results, blot after blot.

WB ECM kit (Rabbit IgG)

LF-QC5002 1 kit
EUR 253
Description: Our Enhanced Chemiluminescent Kit is an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Powered by our proprietary and easy to use substrates, a unique blocking agent, highly specific secondary antibodies, and carefully optimized protocols, this kit offers the highest signal to noise ratio available and yields clean results, blot after blot.

WB ECM kit (Goat IgG)

LF-QC5003 1 kit
EUR 253
Description: Our Enhanced Chemiluminescent Kit is an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Powered by our proprietary and easy to use substrates, a unique blocking agent, highly specific secondary antibodies, and carefully optimized protocols, this kit offers the highest signal to noise ratio available and yields clean results, blot after blot.

WB ECM kit (Rat IgG)

LF-QC5004 1 kit
EUR 253
Description: Our Enhanced Chemiluminescent Kit is an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Powered by our proprietary and easy to use substrates, a unique blocking agent, highly specific secondary antibodies, and carefully optimized protocols, this kit offers the highest signal to noise ratio available and yields clean results, blot after blot.

WB ECM kit (Mouse IgM)

LF-QC5005 1 kit
EUR 253
Description: Our Enhanced Chemiluminescent Kit is an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Powered by our proprietary and easy to use substrates, a unique blocking agent, highly specific secondary antibodies, and carefully optimized protocols, this kit offers the highest signal to noise ratio available and yields clean results, blot after blot.

Polyclonal PSENEN / PEN-2 Antibody (N-Terminus)

APR13001G 0.05mg
EUR 484
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human PSENEN / PEN-2 (N-Terminus). This antibody is tested and proven to work in the following applications:

Ac-Pen-Arg-Gly-Asp-Cys-OH

H-1614.0001 1.0mg
EUR 212
Description: Sum Formula: C22H36N8O9S2; CAS# [135702-36-2]

Ac-Pen-Arg-Gly-Asp-Cys-OH

H-1614.0005 5.0mg
EUR 756
Description: Sum Formula: C22H36N8O9S2; CAS# [135702-36-2]

Total Goat Milk Proteins WB kit

F245 1 kit (application dependant amount of reactions)
EUR 836
  • Product category: Premade blotting kit
Description: Total Goat Milk Proteins WB kit by Cygnus Technologies is available in Europe via Gentaur.

Purified Bovine nRNP WB +ve control

RNP11-C 100 ul
EUR 286

Purified bovineTransferrin Protein WB +ve Control

TF19-C 100 ul
EUR 286

Bovine Ubiquitin protein WB +Ve control

UBQ11-C 100 ul
EUR 286

Human Apolipoprotein B protein control for WB

APOB21-C 100 ul
EUR 286

Rec. Human CD21 protein control for WB

CD21-C 100 ul
EUR 286

Haptoglobin Human Plasma protein control for WB

HGLB18-C 100 ul
EUR 286

Human Heart Ferritin WB +ve protein control

FERT16-C 100 ul
EUR 286

Human Liver Ferritin WB +ve protein control

FERT17-C 100 ul
EUR 286

Purified Flagellin (salmonella) protein control for WB

FLGN17-C 100 ul
EUR 286

Cell Lysis Buffer for WB and IP

abx090622-100ml 100 ml
EUR 217
  • Shipped within 5-10 working days.

Purified Human ceruloplasmin (Cp) WB +ve control

CP11-C 100 ul
EUR 286

Recombinant Mouse Neprilysin protein WB +ve control

NEP11-C 100 ul
EUR 286

Recombinant Human Neprilysin protein WB +ve control

NEP12-C 100 ul
EUR 286

WB DAB Chromogenic Kit (Mouse IgG)-Yellow

LF-QC5006 1 kit
EUR 241
Description: DAB is the chromogenic substrate of peroxidase. The reaction product is a brown precipitate insoluble in water, dimethylbenzene or alcohol, which makes DAB suitable for color development reaction in western blotting. This Western Blotting DAB Chromogenic kit provides an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Our proprietary polymeric labeling of peroxidase conjugated secondary antibodies offers superior sensitivity in western blotting, significant increase in the detection range, high signal‐to‐noise ratio, and lower primary antibodies consumption. Powered by our proprietary polymeric labeling technique, DAB substrates, a unique blocking agent, highly specific secondary antibodies and carefully optimized protocols, this kit yields cleanest results, blot after blot.

WB DAB Chromogenic Kit (Goat IgG)-Yellow

LF-QC5007 1 kit
EUR 241
Description: DAB is the chromogenic substrate of peroxidase. The reaction product is a brown precipitate insoluble in water, dimethylbenzene or alcohol, which makes DAB suitable for color development reaction in western blotting. This Western Blotting DAB Chromogenic kit provides an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Our proprietary polymeric labeling of peroxidase conjugated secondary antibodies offers superior sensitivity in western blotting, significant increase in the detection range, high signal‐to‐noise ratio, and lower primary antibodies consumption. Powered by our proprietary polymeric labeling technique, DAB substrates, a unique blocking agent, highly specific secondary antibodies and carefully optimized protocols, this kit yields cleanest results, blot after blot.

WB DAB Chromogenic Kit (Rabbit IgG)-Yellow

LF-QC5008 1 kit
EUR 241
Description: DAB is the chromogenic substrate of peroxidase. The reaction product is a brown precipitate insoluble in water, dimethylbenzene or alcohol, which makes DAB suitable for color development reaction in western blotting. This Western Blotting DAB Chromogenic kit provides an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Our proprietary polymeric labeling of peroxidase conjugated secondary antibodies offers superior sensitivity in western blotting, significant increase in the detection range, high signal‐to‐noise ratio, and lower primary antibodies consumption. Powered by our proprietary polymeric labeling technique, DAB substrates, a unique blocking agent, highly specific secondary antibodies and carefully optimized protocols, this kit yields cleanest results, blot after blot.

WB DAB Chromogenic Kit (Rat IgG)-Yellow

LF-QC5009 1 kit
EUR 241
Description: DAB is the chromogenic substrate of peroxidase. The reaction product is a brown precipitate insoluble in water, dimethylbenzene or alcohol, which makes DAB suitable for color development reaction in western blotting. This Western Blotting DAB Chromogenic kit provides an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Our proprietary polymeric labeling of peroxidase conjugated secondary antibodies offers superior sensitivity in western blotting, significant increase in the detection range, high signal‐to‐noise ratio, and lower primary antibodies consumption. Powered by our proprietary polymeric labeling technique, DAB substrates, a unique blocking agent, highly specific secondary antibodies and carefully optimized protocols, this kit yields cleanest results, blot after blot.

WB DAB Chromogenic Kit (Mouse IgG)-Blue

LF-QC5010 1 kit
EUR 241
Description: DAB is the chromogenic substrate of peroxidase. The reaction product is a brown precipitate insoluble in water, dimethylbenzene or alcohol, which makes DAB suitable for color development reaction in western blotting. This Western Blotting DAB Chromogenic kit provides an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Our proprietary polymeric labeling of peroxidase conjugated secondary antibodies offers superior sensitivity in western blotting, significant increase in the detection range, high signal‐to‐noise ratio, and lower primary antibodies consumption. Powered by our proprietary polymeric labeling technique, DAB substrates, a unique blocking agent, highly specific secondary antibodies and carefully optimized protocols, this kit yields cleanest results, blot after blot.

WB DAB Chromogenic Kit (Rabbit IgG)-Blue

LF-QC5011 1 kit
EUR 241
Description: DAB is the chromogenic substrate of peroxidase. The reaction product is a brown precipitate insoluble in water, dimethylbenzene or alcohol, which makes DAB suitable for color development reaction in western blotting. This Western Blotting DAB Chromogenic kit provides an easy, consistent, sensitive and highly specific detection solution to your protein of interest. Our proprietary polymeric labeling of peroxidase conjugated secondary antibodies offers superior sensitivity in western blotting, significant increase in the detection range, high signal‐to‐noise ratio, and lower primary antibodies consumption. Powered by our proprietary polymeric labeling technique, DAB substrates, a unique blocking agent, highly specific secondary antibodies and carefully optimized protocols, this kit yields cleanest results, blot after blot.

Purified, Bovine S100 protein control for WB

S1001-C 100 ul
EUR 286

Purified, Human S100 protein control for WB

S1002-C 100 ul
EUR 286

Human Tissue Factor WB +ve protein control

TIF11C 100 ul
EUR 286

Rat Psenen/ Gamma-secretase subunit PEN-2 ELISA Kit

E0809Ra 1 Kit
EUR 646

Mouse Psenen/ Gamma-secretase subunit PEN-2 ELISA Kit

E1216Mo 1 Kit
EUR 632

Human PSENEN/ Gamma-secretase subunit PEN-2 ELISA Kit

E2069Hu 1 Kit
EUR 605

Bovine Gamma- secretase subunit PEN- 2, PSENEN ELISA KIT

ELI-12316b 96 Tests
EUR 928

Human Gamma- secretase subunit PEN- 2, PSENEN ELISA KIT

ELI-16123h 96 Tests
EUR 824

Mouse Gamma- secretase subunit PEN- 2, Psenen ELISA KIT

ELI-45912m 96 Tests
EUR 865

WesternOne? Marker Pen, HRP for Western blot chemiluminescent detection

ACT-WP
EUR 144

Spoligotyping Membrane

IM9702
EUR 1280
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.

Dialysis Membrane

2392344 8unit
EUR 276

Membrane Remover

MVSMR100 Complete
EUR 2653

Monkey (Rhesus) Serum Albumin protein control for WB

ALBMK21-C 100 ul
EUR 286

Monkey (Rhesus) Serum Albumin protein control for WB

ALBMK22-C 100 ul
EUR 286

Human Apolipoprotein C-I protein control for WB

APOC11-C 100 ul
EUR 286

Human Apolipoprotein C-II protein control for WB

APOC22-C 100 ul
EUR 286

Human Apolipoprotein C-III protein control for WB

APOC32-C 100 ul
EUR 286

Human plasma Apolipoprotein E protein control for WB

APOE13-C 100 ul
EUR 286

Human Plasma Apolipoprotein J protein control for WB

APOJ13-C 100 ul
EUR 286

Human Calcineurin A-subunit protein WB +Ve control

CALNA12-C 100 ul
EUR 286

Human Calcineurin B -subunit protein WB +Ve control

CALNB21-C 100 ul
EUR 286

Purified human Catalase (CATL) protein control for WB

CATL11-C 100 ul
EUR 286

Human nth Endonuclease III (hNTH1) WB +ve control

hNTH11-C 100 ul
EUR 286

Purified Human Neutrophil Elastase protein control for WB

ESTE11-C 100 ul
EUR 286

Bovine Adenosine receptor 2a (A2aR) WB Positive Control

A2aR21-Cb 100 ul
EUR 225

Recombinant purified Firefly Luciferase protein WB +ve control

LUCF11-C 100 ul
EUR 286

p300 protein WB +ve control (HeLa nuclear extract)

P3001-C 100 ul
EUR 286

Mouse Recombinant purified Resistin protein WB +ve control

RSTN11-C 100 ul
EUR 286

Human Recombinant purified Resistin protein WB +ve control

RSTN12-C 100 ul
EUR 286

Human Salivary Amylase protein positive control for WB

SAMY16-C 100 ul
EUR 286

Recombinant other HPSE WB Protein, Untagged, E.coli-100ng

QP12305-100ng 100ng
EUR 517

Recombinant other HPSE WB Protein, Untagged, E.coli-200ng

QP12305-200ng 200ng
EUR 962

Recombinant other HPSE WB Protein, Untagged, E.coli-300ng

QP12305-300ng 300ng
EUR 1415

Purified, recombinant Human TACE control protein for WB

TACE11-C 100 ul
EUR 286

Purified Human Survivin protein for WB +ve control

SURV11-C 100 ul
EUR 286

Purified Human Smith Antigen (Sm) WB +ve control

SMA11-C 100 ul
EUR 286

Purified Human Holo-Transferrin Protein WB +ve Control

TF11-C 100 ul
EUR 286

Purified Rat Apo-Transferrin Protein WB +ve Control

TF12-C 100 ul
EUR 286

Purified Mouse Apo-Transferrin Protein WB +ve Control

TF14-C 100 ul
EUR 286

Recombinant Human SSB/La protein WB +ve control

SSB523-C 100 ul
EUR 286

Human Apoptosis Inducing Factor (AIF) WB +ve protein control

AIF12-C 100 ul
EUR 286

Mouse Angiopoietin 3 (Ang-3) protein control for WB

ANG31-C 100 ul
EUR 286

Human Angiopoietin 4 (Ang-4) protein control for WB

ANG41-C 100 ul
EUR 286

Apolipoprotein A-Il, Human Plasma protein control for WB

APOA21-C 100 ul
EUR 286

Purified Human beta-2 microglobulin (B2M) WB +ve control

B2M11-C 100 ul
EUR 286

Human recombinant purified BMP-1 protein control for WB

BMP12-C 100 ul
EUR 286

Human Ferritin (H-chain) recombinant protein WB +ve control

FERH13-C 100 ul
EUR 286

Human Ferritin (L-chain) recombinant protein WB +ve control

FERL14-C 100 ul
EUR 286

Purified rat liver Ferritin protein WB +ve protein control

FERT25-C 100 ul
EUR 286

Purified mouse liver Ferritin protein WB +ve protein control

FERT31-C 100 ul
EUR 286

Alpha 2-Macroglobulin (A2M), Human protein control for WB

A2MG11-C 100 ul
EUR 286
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.

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