Human Anti-HIV-1 gp120 V3 Recombinant Antibody (clone 2424) (CAT#: PABL-176)

Recombinant Human Antibody (2424) is capable of binding to HIV-1 gp120 V3, expressed in HEK 293 cells. Expressed as the combination of a heavy chain (HC) containing VH from anti-HIV-1 gp120 V3 mAb and CH1-3 region of human IgG1 and a light chain (LC) encoding VL from anti-HIV-1 gp120 V3 mAb and CL of human light chain. Exists as a disulfide linked dimer of the HC and LC hetero-dimer under non-reducing condition. This antibody achieves 100% neutralization against JRFL.


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Figure 1 Neutralization potency of 2424 versus the other V3-specific MAbs against JRFL.

Figure 1 Neutralization potency of 2424 versus the other V3-specific MAbs against JRFL.

Titration curves of the six V3 MAbs against JRFL. Neutralization assay was performed with JRFL pseudovirus and TZM.bl cells. MAbs were titrated and incubated with virus at 37°C for 1 h. TZM.bl cells were then added to the virus-MAb mixtures in DMEM containing 10% fetal bovine serum and DEAE-dextran. Neutralization activity was assessed 48 h later using the luciferase detection system. The parvovirus-specific MAb 1418 was included as a negative control.

Kumar, R., Pan, R., Upadhyay, C., Mayr, L., Cohen, S., Wang, X. H.,... & Gorny, M. K. (2015). Functional and structural characterization of human V3-specific monoclonal antibody 2424 with neutralizing activity against HIV-1 JRFL.Journal of virology, JVI-01280.

Figure 2 Effects of CD4 engagement on virus neutralization by 2424 versus the other V3 MAbs.

Figure 2 Effects of CD4 engagement on virus neutralization by 2424 versus the other V3 MAbs.

Neutralization of JRFL pseudovirus by V3 MAbs 2424, 447-52D, 3074, and 3869 was evaluated after treatment with or without sCD4. Virus was pretreated with 2.5 μg/ml of sCD4 for 30 min at 37°C or left untreated and then incubated with serially diluted MAb for 1 h at 37°C. TZM.bl cells were added to virus-MAb mixtures in DMEM containing 10% fetal bovine serum and DEAE-dextran. After 48 h, virus infection was measured based on β-galactosidase activity.

Kumar, R., Pan, R., Upadhyay, C., Mayr, L., Cohen, S., Wang, X. H.,... & Gorny, M. K. (2015). Functional and structural characterization of human V3-specific monoclonal antibody 2424 with neutralizing activity against HIV-1 JRFL.Journal of virology, JVI-01280.

Figure 3 Neutralization activities of 2424 versus the other V3 MAbs against HIV-1 pseudoviruses expressing wild-type or mutant JRFL Envs.

Figure 3 Neutralization activities of 2424 versus the other V3 MAbs against HIV-1 pseudoviruses expressing wild-type or mutant JRFL Envs.

HIV-1 JRFL pseudoviruses bearing wild-type or mutated Envs were produced in transfected 293T cells and incubated by titrated V3 MAbs (2424, 447-52D, 2219, 2557, 3074, and 3869) for 1 h at 37°C. TZM.bl cells were then added to the virus-MAb mixtures in complete DMEM containing DEAE-dextran. Neutralization activity was assessed after 48 h.

Kumar, R., Pan, R., Upadhyay, C., Mayr, L., Cohen, S., Wang, X. H.,... & Gorny, M. K. (2015). Functional and structural characterization of human V3-specific monoclonal antibody 2424 with neutralizing activity against HIV-1 JRFL.Journal of virology, JVI-01280.

Figure 4 Binding of MAb 2424 to gp120 proteins of clade B and clade C HIV-1 isolates.

Figure 4 Binding of MAb 2424 to gp120 proteins of clade B and clade C HIV-1 isolates.

The binding of MAbs (1 μg/ml) to gp120 used at 1 μg/ml to coat the well surface was detected by ELISA. An irrelevant control MAb, MAb 1418, was also tested in parallel and displayed no binding to any gp120 in the panel (OD405 ≤ 0.2; data not shown).

Kumar, R., Pan, R., Upadhyay, C., Mayr, L., Cohen, S., Wang, X. H.,... & Gorny, M. K. (2015). Functional and structural characterization of human V3-specific monoclonal antibody 2424 with neutralizing activity against HIV-1 JRFL.Journal of virology, JVI-01280.

Figure 5 Neutralizing activities of MAb 2424 versus the other V3 MAbs against JRFL produced in the presence or absence of a mannosidase inhibitor

Figure 5 Neutralizing activities of MAb 2424 versus the other V3 MAbs against JRFL produced in the presence or absence of a mannosidase inhibitor

(A) HIV-1 JRFL pseudoviruses were produced in transfected 293T cells in the absence or presence of 25 μM kifunensine (JRFLKif) and tested for neutralization by V3 MAbs (2424, 447-52D, 2219, 2557, 3869, and 3074), MAb 2G12, CD4bs MAb b12, or an irrelevant MAb, MAb 1418. (B) HIV-1 JRFL pseudoviruses were produced in 293T cells with or without 20 μM swainsonine (JRFLSwain) and tested for neutralization by V3 MAbs 2424 and 447-52D. Serially diluted MAbs were incubated with virus at 37°C for 1 h. TZM.bl cells were then added to the virus-MAb mixtures in complete DMEM containing DEAE-dextran. Neutralization activity was assessed after 48 h. Results with 2424 and 447-52D were averages from duplicate wells, and data from one representative experiment are shown. (C) V3 MAb reactivity with gp120 JRFL was assessed in ELISA. Recombinant gp120 protein (1 μg/ml) was coated on 96-well plates and reacted with serially diluted V3 MAbs.

Kumar, R., Pan, R., Upadhyay, C., Mayr, L., Cohen, S., Wang, X. H.,... & Gorny, M. K. (2015). Functional and structural characterization of human V3-specific monoclonal antibody 2424 with neutralizing activity against HIV-1 JRFL.Journal of virology, JVI-01280.


Specifications

  • Host Species
  • Human
  • Type
  • Human IgG1, κ
  • Species Reactivity
  • HIV-1
  • Clone
  • 2424
  • Applications
  • WB, ELISA, FuncS

Product Property

  • Purity
  • >95% as determined by SDS-PAGE
  • Concentration
  • Please refer to the vial label for the specific concentration.
  • Buffer
  • PBS
  • Preservative
  • No preservatives
  • Storage
  • Centrifuge briefly prior to opening vial. Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Applications

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

Target

  • Alternative Names
  • ENV; gp160; envelope glycoprotein; Envelope surface glycoprotein gp160; precursor; hypothetical protein; Envelope surface glycoprotein gp120; Envelope transmembrane domain

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.

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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.

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