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Mouse anti his capture antibody

Manufactured by Thermo Fisher Scientific

The mouse anti-HIS capture antibody is a laboratory reagent used to detect and purify proteins with a histidine (HIS) tag. It is a monoclonal antibody that specifically binds to the HIS tag, allowing for the isolation and identification of HIS-tagged proteins from complex samples. The core function of this product is to facilitate the capture and isolation of HIS-tagged proteins for various research and analytical applications.

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2 protocols using mouse anti his capture antibody

1

ELISA Quantification of Antibody Binding

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Antibodies b12, 2G12, PGT121, PGT128 and PGT135 were obtained from the International AIDS Vaccine Initiative (IAVI, New York, NY). Microtitre ELISA plates (Corning) were coated with mouse anti-HIS capture antibody (2 μg mL−1 in PBS; Life Technologies) overnight at 4 °C. Plates were washed five times with a solution of PBS containing 0.05% Tween 20 (v/v) and then blocked for 1 h at room temperature with 5% non-fat milk in PBS + 0.05% Tween (blocking buffer). Gp120 was then added at a concentration of 2 μg ml−1 in blocking buffer, followed by incubation for 1 h at room temperature. Plates were washed (×5) before addition of primary antibodies (b12, 17b, 2G12, PGT121, PGT128 & PGT135). A 1:5 dilution series was used starting at 20 μg ml−1 or 40 μg ml−1 in blocking buffer. Incubation was carried out at room temperature for 2 h. Plates were then washed (×5) and alkaline phosphatase-conjugated goat anti-human Fab secondary antibody (Thermo Scientific Pierce) was added as a 1:1000 dilution in blocking buffer. Plates were washed (×5) and then AP substrate (50 μL per well) was added. Once color had developed the OD at 405 nm was measured.
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2

ELISA Quantification of Antibody Binding

Check if the same lab product or an alternative is used in the 5 most similar protocols
Antibodies b12, 2G12, PGT121, PGT128 and PGT135 were obtained from the International AIDS Vaccine Initiative (IAVI, New York, NY). Microtitre ELISA plates (Corning) were coated with mouse anti-HIS capture antibody (2 μg mL−1 in PBS; Life Technologies) overnight at 4 °C. Plates were washed five times with a solution of PBS containing 0.05% Tween 20 (v/v) and then blocked for 1 h at room temperature with 5% non-fat milk in PBS + 0.05% Tween (blocking buffer). Gp120 was then added at a concentration of 2 μg ml−1 in blocking buffer, followed by incubation for 1 h at room temperature. Plates were washed (×5) before addition of primary antibodies (b12, 17b, 2G12, PGT121, PGT128 & PGT135). A 1:5 dilution series was used starting at 20 μg ml−1 or 40 μg ml−1 in blocking buffer. Incubation was carried out at room temperature for 2 h. Plates were then washed (×5) and alkaline phosphatase-conjugated goat anti-human Fab secondary antibody (Thermo Scientific Pierce) was added as a 1:1000 dilution in blocking buffer. Plates were washed (×5) and then AP substrate (50 μL per well) was added. Once color had developed the OD at 405 nm was measured.
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