Anti ha mouse monoclonal antibody mab

Manufactured by Fortrea

Sourced in United States

The Anti-HA mouse monoclonal antibody (mAb) is a laboratory reagent used for the detection and purification of proteins tagged with the hemagglutinin (HA) epitope. It specifically binds to the HA tag, allowing for the identification and isolation of HA-tagged proteins in various experimental procedures.

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Lab products found in correlation

Anti tubulin mouse mab, by Fortrea (3 mentions) Anti p24 mouse mab, by Merck Group (2 mentions) Alkaline phosphatase conjugated goat anti rabbit or anti mouse immunoglobulin g secondary antibodies, by Jackson ImmunoResearch (2 mentions) Mouse anti flag mab, by Merck Group (2 mentions) Anti his mouse mab, by Merck Group (1 mentions) Alexa fluor 488 goat anti mouse igg secondary antibody, by Thermo Fisher Scientific (1 mentions) Anti gapdh rabbit polyclonal antibody, by Affinity Biosciences (1 mentions) Anti cmyc mouse mab, by Merck Group (1 mentions)

3 protocols using anti ha mouse monoclonal antibody mab

Antibody Usage in Biological Research

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The following antibodies were used in this study: anti-HA mouse monoclonal antibody (mAb) (Covance, Emeryville, CA, USA), anti-tubulin mouse mAb (Covance), anti-His mouse mAb (Sigma, St. Louis, MO, USA) and anti-p24 mouse mAb obtained from an HIV-1 p24 hybridoma from the National Institutes of Health AIDS Research and Reference Reagent Program (NIH-ARRRP).
Alkaline phosphatase conjugated goat anti-rabbit or anti-mouse immunoglobulin G secondary antibodies were purchased from Jackson ImmunoResearch Laboratories (West Grove, PA, USA). Alexa Fluor 488 goat anti-mouse IgG secondary antibodies and Alexa Fluor 633 goat anti-rabbit IgG secondary antibodies were from Invitrogen.

Wang W., Wang J., Qu M., Li X., Zhang J., Zhang H., Wu J., Yu B., Wu H., Kong W, & Yu X. (2015). Viral Restriction Activity of Feline BST2 Is Independent of Its N-Glycosylation and Induction of NF-κB Activation. PLoS ONE, 10(9), e0138190.

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Antibody Characterization and Detection

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The following antibodies were used: anti-HA mouse monoclonal antibody (mAb) (Covance), anti-tubulin mouse mAb (Covance), anti-NF-κB 1 mouse mAb (Affinity Bioscience), anti-NF-κB p65 rabbit polyclonal antibody (Affinity Bioscience), anti-GAPDH rabbit polyclonal antibody (Affinity Bioscience), anti-Histone H3 rabbit polyclonal antibody (Proteintech), anti-Flag mouse mAb (Sigma), and anti-p24 mouse mAb obtained from an HIV-1 p24 hybridoma from the National Institutes of Health AIDS Research and Reference Reagent Program. Alkaline phosphatase-conjugated goat anti-rabbit or anti-mouse immunoglobulin G secondary antibodies were purchased from Jackson ImmunoResearch Laboratories (West Grove).

Qu M., Wang W., Li W., Cao J., Zhang X., Wang C., Wu J., Yu B., Zhang H., Wu H., Kong W, & Yu X. (2020). Antiviral Activity of Feline BCA2 Is Mainly Dependent on Its Interference With Proviral Transcription Rather Than Degradation of FIV Gag. Frontiers in Microbiology, 11, 1230.

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Antibody Panel for Protein Analysis

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The following antibodies were used in the present study: anti-HA mouse monoclonal antibody (mAb; Covance, Emeryville, CA), anti-cmyc mouse mAb (Millipore, Billerica, MA), anti-Flag mouse mAb (Sigma, St. Louis, MO), anti-tubulin mouse mAb (Covance), anti-Cul2 rabbit polyclonal antibody (pAb; Santa Cruz Biotechnology, Santa Cruz, CA), anti-Cul5 rabbit pAb (Santa Cruz Biotechnology), anti-CBF-β mouse mAb (Santa Cruz Biotechnology), anti-EloB rabbit pAb (Santa Cruz Biotechnology) and anti-EloC mouse mAb (Santa Cruz Biotechnology).

Zhang J., Wu J., Wang W., Wu H., Yu B., Wang J., Lv M., Wang X., Zhang H., Kong W, & Yu X. (2014). Role of cullin-elonginB-elonginC E3 complex in bovine immunodeficiency virus and maedi-visna virus Vif-mediated degradation of host A3Z2-Z3 proteins. Retrovirology, 11, 77.

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