Recombinant Human Anti-HCV E2 Antibody (MRCT10.v362) (CAT#: PABL-124)

Recombinant Human neutralizing Antibody (MRCT10.v362) is capable of binding to a highly conserved linear epitope on E2, expressed in HEK 293 cells. Expressed as the combination of a heavy chain (HC) containing VH from anti-HCV E2 mAb and CH1-3 region of human IgG1 and a light chain (LC) encoding VL from anti-HCV E2 mAb and CL of human kappa light chain. Exists as a disulfide linked dimer of the HC and LC hetero-dimer under non-reducing condition.


Specific Inquiry
  • Size:
  • Conjugation:
  • Endotoxin:
  • Purity:
  • Fc Engineering:
  • Published Data
  • Datasheet
  • MSDS
  • COA

Figure 2 (a) Ratio of dissociation constants (KD) for MRCT10.v362 (red) and hu5B3.v3 (black) binding to alanine mutant peptides relative to WT peptide QLINTNGSWHINGSGK-biotin (E2412–423-biotin) are graphed. Asterisks denote no binding detected with mutant peptides.

Figure 2 (a) Ratio of dissociation constants (KD) for MRCT10.v362 (red) and hu5B3.v3 (black) binding to alanine mutant peptides relative to WT peptide QLINTNGSWHINGSGK-biotin (E2412–423-biotin) are graphed. Asterisks denote no binding detected with mutant peptides.

Pantua, H., Diao, J., Ultsch, M., Hazen, M., Mathieu, M., McCutcheon, K.,... & Hass, P. (2013). Glycan shifting on hepatitis C virus (HCV) E2 glycoprotein is a mechanism for escape from broadly neutralizing antibodies. Journal of molecular biology, 425(11), 1899-1914.

Figure 3 (b) Binding of various E2412–423-specific neutralizing antibodies to lysates of untransfected 293 cells (No E2) or 293 cells transfected with genotype 2a (J6CF) HCV E1E2-expressing plasmids containing various mutations at N415 or N417.

Figure 3 (b) Binding of various E2412–423-specific neutralizing antibodies to lysates of untransfected 293 cells (No E2) or 293 cells transfected with genotype 2a (J6CF) HCV E1E2-expressing plasmids containing various mutations at N415 or N417.

Pantua, H., Diao, J., Ultsch, M., Hazen, M., Mathieu, M., McCutcheon, K.,... & Hass, P. (2013). Glycan shifting on hepatitis C virus (HCV) E2 glycoprotein is a mechanism for escape from broadly neutralizing antibodies. Journal of molecular biology, 425(11), 1899-1914.

Figure 4 (c and d) MRCT10 Fab binds to N417S E2412–423. Biacore sensorgrams demonstrating binding of MRCT10 Fab to WT (c) or N417S (d) E2412–423 peptide. The Fab series was diluted 2-fold starting from 1000 nM down to 15.6 nM. MRCT10 Fab binds to N417S E2412–423 peptide with faster off-rate compared to WT. Dissociation constants (KD) are listed in the graphs.

Figure 4 (c and d) MRCT10 Fab binds to N417S E2412–423. Biacore sensorgrams demonstrating binding of MRCT10 Fab to WT (c) or N417S (d) E2412–423 peptide. The Fab series was diluted 2-fold starting from 1000 nM down to 15.6 nM. MRCT10 Fab binds to N417S E2412–423 peptide with faster off-rate compared to WT. Dissociation constants (KD) are listed in the graphs.

Pantua, H., Diao, J., Ultsch, M., Hazen, M., Mathieu, M., McCutcheon, K.,... & Hass, P. (2013). Glycan shifting on hepatitis C virus (HCV) E2 glycoprotein is a mechanism for escape from broadly neutralizing antibodies. Journal of molecular biology, 425(11), 1899-1914.

Figure 5 Enhancement of antiviral effect of NS3 protease inhibitors by inhibition of HCV entry. DMSO-differentiated Huh7.5 cells were infected with Jc1 HCVcc (MOI = 0.05) alone (filled squares) or in the presence of MRCT10.v362 (10 μg/mL, open circles), Telaprevir (2 μM, open triangles) or a combination of MRCT10.v362 and Telaprevir (open diamonds). HCV RNA copies were measured at various times post infection. HCV cDNA derived from the day 22 post infection cultures was sequenced (denoted by the asterisk).

Figure 5 Enhancement of antiviral effect of NS3 protease inhibitors by inhibition of HCV entry. DMSO-differentiated Huh7.5 cells were infected with Jc1 HCVcc (MOI = 0.05) alone (filled squares) or in the presence of MRCT10.v362 (10 μg/mL, open circles), Telaprevir (2 μM, open triangles) or a combination of MRCT10.v362 and Telaprevir (open diamonds). HCV RNA copies were measured at various times post infection. HCV cDNA derived from the day 22 post infection cultures was sequenced (denoted by the asterisk).

Pantua, H., Diao, J., Ultsch, M., Hazen, M., Mathieu, M., McCutcheon, K.,... & Hass, P. (2013). Glycan shifting on hepatitis C virus (HCV) E2 glycoprotein is a mechanism for escape from broadly neutralizing antibodies. Journal of molecular biology, 425(11), 1899-1914.


Specifications

  • Immunogen
  • Hepatitis C virus E2 envelope protein
  • Host Species
  • Human
  • Derivation
  • Human
  • Type
  • IgG
  • Specificity
  • Tested positive against native HCV E2
  • Species Reactivity
  • HCV
  • Clone
  • MRCT10.v362
  • Applications
  • WB, ELISA, IF, FuncS

Product Property

  • Purity
  • >95% by SDS-PAGE and HPLC analysis
  • Storage
  • Store the antibody (in aliquots) at -20°C. Avoid repeated freezing and thawing of samples.

Applications

  • Application Notes
  • The antibody was validated for ELISA and FuncS. For details, refer to published data.

Target

  • Alternative Names
  • E2; HCV; envelope protein; hepatitis C virus

Product Notes

This is a product of Creative Biolabs' Hi-Affi™ recombinant antibody portfolio, which has several benefits including:

• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production

See more details about Hi-Affi™ recombinant antibody benefits.

Downloads

Download resources about recombinant antibody development and antibody engineering to boost your research.

See other products for "Clone MRCT10.v362"

See other products for "E2"

Single-domain Antibody

CAT Product Name Application Type
PNBL-019 Recombinant Anti-HCV E2 VHH Single Domain Antibody (D03) Inhib, FuncS Llama VHH

Human Antibody

Customer Reviews and Q&As

Submit a review or a question
There are currently no Customer reviews or questions for PABL-124. Click the button above to contact us or submit your feedback about this product.
View the frequently asked questions answered by Creative Biolabs Support.

For Research Use Only. Not For Clinical Use.

For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

Send Inquiry

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

© 2024 Creative Biolabs.
  • 0
  • 0
Cart

    Go to compare