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Horseradish peroxidase conjugated goat anti human fc specific polyclonal igg

Manufactured by Merck Group
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Horseradish peroxidase conjugated goat anti-human Fc specific polyclonal IgG is a laboratory reagent used for detection and quantification of human antibodies in various immunoassays. It consists of polyclonal goat antibodies that specifically recognize the Fc region of human immunoglobulin G (IgG), conjugated to the enzyme horseradish peroxidase.

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Lab products found in correlation

Goat rabbit anti human α chain specific polyclonal iga, by Merck Group (2 mentions)

Spelling variants of this product

Horseradish peroxidase-conjugated goat anti-human IgG (14 citations) Peroxidase-conjugated goat anti-human IgG (12 citations) Peroxidase-conjugated anti-human IgG (11 citations) Horseradish-peroxidase-conjugated anti-human IgG (9 citations) Goat anti-human IgG-Fc (6 citations) Goat anti-Human IgG (Fc specific) (4 citations) IgG-Fc Specific-Peroxidase (4 citations) Peroxidase-conjugated anti-human Fc (3 citations) Peroxidase-conjugated human Fc-specific IgG (2 citations) Polyclonal human IgG (2 citations)

2 protocols using horseradish peroxidase conjugated goat anti human fc specific polyclonal igg

1

Evaluating SARS-CoV-2 Spike Protein Antibodies

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
Titers of plasma IgG and mucosal sIgA against the spike protein (S) of SARS-CoV-2 prototype strain and BA.1, BA.1.1, BA.2, BA.2.12.1, BA.2.75, and BA.4/5 were evaluated using the enzyme-linked immunosorbent assay (ELISA) as previously reported [13 (link)]. The optimal coating concentration of S protein of SARS-CoV-2 prototype strain and Omicron sublineages (ACROBiosystems, Beijing, China) were 50 ng. The optimal plasma dilutions were 1/400. The second antibodies were horseradish peroxidase conjugated goat anti-human Fc specific polyclonal IgG or goat rabbit anti-human α chain specific polyclonal IgA (Sigma Aldrich, St Louis, MO, USA), respectively.
Guo L., Zhang Q., Zhong J., Chen L., Jiang W., Huang T., Li Y., Zhang Y., Xu L., Wang X., Xiao Y., Wang Y., Dong X., Dong T., Peng Y., Zhang B., Xie Y., Gao H., Shen Z., Ren L., Cheng T, & Wang J. (2023). Omicron BA.1 breakthrough infections in inactivated COVID-19 vaccine recipients induced distinct pattern of antibody and T cell responses to different Omicron sublineages. Emerging Microbes & Infections, 12(1), 2202263.
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2

Evaluating SARS-CoV-2 Spike Protein Antibodies

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
Titers of plasma IgG and mucosal sIgA against the spike protein (S) of SARS-CoV-2 prototype strain and BA.1, BA.1.1, BA.2, BA.2.12.1, BA.2.75, and BA.4/5 were evaluated using the enzyme-linked immunosorbent assay (ELISA) as previously reported [13 (link)]. The optimal coating concentration of S protein of SARS-CoV-2 prototype strain and Omicron sublineages (ACROBiosystems, Beijing, China) were 50 ng. The optimal plasma dilutions were 1/400. The second antibodies were horseradish peroxidase conjugated goat anti-human Fc specific polyclonal IgG or goat rabbit anti-human α chain specific polyclonal IgA (Sigma Aldrich, St Louis, MO, USA), respectively.
Guo L., Zhang Q., Zhong J., Chen L., Jiang W., Huang T., Li Y., Zhang Y., Xu L., Wang X., Xiao Y., Wang Y., Dong X., Dong T., Peng Y., Zhang B., Xie Y., Gao H., Shen Z., Ren L., Cheng T, & Wang J. (2023). Omicron BA.1 breakthrough infections in inactivated COVID-19 vaccine recipients induced distinct pattern of antibody and T cell responses to different Omicron sublineages. Emerging Microbes & Infections, 12(1), 2202263.
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