Suitable for WB, Dot, IHC-Fr, IHC-P, IM, ICC/IF, ELISA. Ideal for western blot. Cited in 1 publication.
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application WB | Reactivity Expected | Dilution info - | Notes - |
Application Dot | Reactivity Expected | Dilution info - | Notes - |
Application IHC-Fr | Reactivity Expected | Dilution info - | Notes - |
Application IHC-P | Reactivity Expected | Dilution info - | Notes - |
Application IM | Reactivity Expected | Dilution info - | Notes - |
Application ICC/IF | Reactivity Expected | Dilution info 1/500 - 1/2500 | Notes - |
Application ELISA | Reactivity Reacts | Dilution info 1/10000 - 1/50000 | Notes - |
Ig gamma 1 chain C region, Ig gamma 3 chain C region, Ig gamma 4 chain C region, Ig gamma-2 chain C region, Immunoglobin heavy constant gamma 1, Immunoglobulin G
Suitable for WB, Dot, IHC-Fr, IHC-P, IM, ICC/IF, ELISA. Ideal for western blot. Cited in 1 publication.
Preservative: 0.01% Gentamicin sulphate
Constituents: 1% Polyethylene glycol, 0.88% Sodium chloride, 0.424% Potassium phosphate solution
Anti-Bovine IgG antibody was prepared from monospecific antiserum by immunoaffinity chromatography using Bovine IgG coupled to agarose beads.
This HRP conjugate antibody may have a small amount of sediments or cloudiness in the buffer.
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ELISA results of ab6927 against purified Bovine IgG HRP. Each well was coated in duplicate with 1.0 µg of Bovine IgG. The working dilution is 1/102,000. The starting dilution of antibody was 5 µg/ml and the X-axis represents the Log10 of a 3-fold dilution. This titration is a 4-parameter curve fit where the IC50 is defined as the titer of the antibody. Assay performed using HRP Conjugation Stabilizer and TMB substrate.
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