Suitable for IHC-P, ICC, ELISA, WB. Ideal for western blot. Preadsorbed to minimise non-specific binding and high background staining. Cited in 1 publication.
| Application | Reactivity | Dilution info | Notes |
|---|---|---|---|
Application IHC-P | Reactivity Reacts | Dilution info 1/200.00000 - 1/5000.00000 | Notes - |
Application ICC | Reactivity Reacts | Dilution info 1/200.00000 - 1/5000.00000 | Notes - |
Application ELISA | Reactivity Reacts | Dilution info 1/10000.00000 - 1/100000.00000 | Notes (as primary). |
Application WB | Reactivity Reacts | Dilution info 1/5000.00000 - 1/50000.00000 | Notes Colorimetric: 1/5000 - 1/30000; Chemiluminescent: 1/10000 - 1/50000. |
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 IHC-P, ICC, ELISA, WB. Ideal for western blot. Preadsorbed to minimise non-specific binding and high background staining. Cited in 1 publication.
By immunoelectrophoresis and ELISA this antibody reacts specifically with bovine IgG and with light chains common to other bovine immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. Reduced cross-reactivity to human, mouse and rat IgG was detected. This antibody may cross react with IgG from other species.
pH: 6.8 - 7.4
Preservative: 0.05% CMIT/MIT based preservative
Antiserum was cross adsorbed using human, mouse and rat immunosorbents to remove cross reactive antibodies. This antibody was isolated by affinity chromatography using antigen coupled to agarose beads and conjugated to Horse Radish Peroxidase.
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