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Goat anti human igg hrp secondary antibody

Manufactured by Southern Biotech

The Goat anti-human IgG-HRP secondary antibody is a laboratory tool used in immunoassays. It is a conjugate of a goat-derived antibody that binds to human immunoglobulin G (IgG) and the enzyme horseradish peroxidase (HRP). This antibody-enzyme complex can be used to detect and quantify the presence of human IgG in samples.

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2 protocols using goat anti human igg hrp secondary antibody

1

Viral Vector Antigenicity Evaluation

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To analyze both the exposure and antigenicity of V2 on viral vectors, vectors (7 × 109 VP for Ad, Ad-HVR1-20aa-V2 and Ad-HVR1-V2, and 2.1 × 1010 VP for Ad-pIX-V1V2) were mixed with 4x native loading buffer without boiling, and resolved on native PAGE gels, followed by transfer and blocking on PVDF membrane. Blotting was performed with HIV-1 205 F strain-derived hMAb 6.4 C (1:1,000), and with goat anti-human IgG-HRP secondary antibody (1:2000; Southern biotech, Birmingham, AL). The proteins were detected by using 3′3′-diaminobenzidine tablets (Sigma-Aldrich, MO) (Gu et al., 2013 (link)).
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2

Quantifying Adenoviral Capsid Antigenicity

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The whole virus ELISAs were performed as described elsewhere (Gu et al., 2013 (link)), in order to investigate both the exposure and antigenicity of V2 on surface of capsid. Briefly, different amounts of vectors (2 × 109 VP/well for Ad-HVR1-20aa-V2 and Ad-HVR1-V2, and 6 × 109 VP/well for Ad and Ad-pIX-V1V2) were immobilized and blocked. The immobilized vectors were incubated with hMAb 6.4 C (1:1,000), followed by incubation with goat anti-human IgG-HRP secondary antibody (1:2000; Southern biotech, Birmingham, AL). ELISAs were developed with the SIGMAFAST OPD peroxidase substrate (Sigma-Aldrich, MO) and measured at OD 450 nm.
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