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Goat anti mouse igg fc biotin conjugate

Manufactured by Thermo Fisher Scientific

Goat anti-mouse IgG Fc biotin conjugate is a secondary antibody reagent used in various immunoassay and immunochemical techniques. It is generated by conjugating biotin to the Fc region of goat-derived antibodies specific to the Fc portion of mouse immunoglobulin G (IgG) molecules.

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2 protocols using goat anti mouse igg fc biotin conjugate

1

JUNV GP1 Antibody Binding ELISA

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High-binding ELISA 96-half-well microplates (Corning) were coated with purified JUNV GP1 (25 μL, 3 μg/mL in PBS) overnight at 4°C. Plates were washed five times with PBS-T (0.05% Tween 20) and blocked with blocking buffer (5% nonfat milk in PBS-T) for 1 h at room temperature. The blocking buffer was removed, and serially diluted JUN1 Fab (at 50 μg/mL, 1:5 dilution in blocking buffer) was added for 30 min at room temperature. JUN1 to JUN7 IgG was added at the 80% effective concentration (EC80) and incubated for a further 1.5 h. Plates were washed five times with PBS-T. Secondary antibody (goat anti-mouse IgG Fc biotin conjugate; Thermo Fisher Scientific; 1:1,000) was added for 30 min, plates were washed as described above, and streptavidin-AP (1:10,000; Invitrogen) was added for 30 min. Following a final wash, p-nitrophenyl phosphate substrate (Sigma) was added to detect binding and the ODs were measured at 405 nm. The competition is reported for JUN1 Fab at 50 μg/mL and is reported relative to the percent competition measured for JUN1 IgG.
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2

ELISA Protocol for Viral GP1 Detection

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ELISAs were carried out as previously described (27 (link)). High-binding ELISA 96-half-well microplates (Corning) were coated with purified JUNV GP1 or MACV GP1 (25 μL, 3 μg/mL in phosphate-buffered saline [PBS]) overnight at 4°C. Plates were washed five times with PBS containing 0.05% Tween 20 (PBS-T) and blocked with blocking buffer (5% nonfat milk in PBS-T) for 1 h at room temperature. The blocking buffer was removed, and serially diluted Ab (starting at 10 μg/mL, 1:5 dilution in blocking buffer) was added for 2 h at room temperature. Plates were washed five times with PBS-T. Secondary Ab (goat anti-mouse IgG Fc, biotin conjugate; Thermo Fisher Scientific; 1:1,000) was added for 30 min, plates were washed as described above, and alkaline phosphatase (AP)-conjugated streptavidin (1:10,000; Invitrogen) was added for 30 min. Following a final wash, p-nitrophenyl phosphate substrate (Sigma) was added to detect binding, and the optical densities (ODs) were measured at 405 nm.
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