Goat Anti-Mouse IgG H&L (Biotin) is a secondary antibody that is suitable for Western blot, IHC, ICC/IF, ELISA and more.
- Cited in over 80 publications
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application ICC | Reactivity Expected | Dilution info - | Notes - |
Application Dot | Reactivity Expected | Dilution info - | Notes - |
Application IHC-Fr | Reactivity Expected | Dilution info - | Notes - |
Application IHC-P | Reactivity Reacts | Dilution info - | Notes - |
Application IM | Reactivity Expected | Dilution info - | Notes - |
Application ELISA | Reactivity Reacts | Dilution info 1/350000 | Notes - |
Application WB | Reactivity Expected | Dilution info 1/2000 - 1/20000 | Notes - |
Application ICC/IF | Reactivity Expected | Dilution info 1/1000 - 1/5000 | Notes - |
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Igh-4, Ighg1, Ig gamma-1 chain C region secreted form
Goat Anti-Mouse IgG H&L (Biotin) is a secondary antibody that is suitable for Western blot, IHC, ICC/IF, ELISA and more.
- Cited in over 80 publications
Preservative: 0.01% Sodium azide
Constituents: 1% BSA, 0.88% Sodium chloride, 0.424% Potassium phosphate solution
This product was prepared from monospecific antiserum by immunoaffinity chromatography using Mouse IgG coupled to agarose.
This antibody reacts with the heavy and light chains of Mouse IgG
When it comes to advancing your immunohistochemistry (IHC) research, Abcam offers comprehensive suite of IHC kits and secondary antibodies , designed to deliver precise and reliable results.
The conjugate is expected to have between 5 and 10 moles of biotin per mole of IgG.
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Full details and terms and conditions can be found here:
Terms & Conditions.
The section was pre-treated using pressure cooker heat mediated antigen retrieval with sodium citrate buffer (pH 6) for 30 mins. The section was then incubated with Anti-Histone H1.0 antibody [27] ab11080, 1/1,000 dilution, for 15 mins at room temperature. A goat anti-mouse biotinylated secondary antibody (ab6788, 1/1000 dilution), was used to detect the primary, and visualized using an HRP conjugated ABC system. Streptavidin HRP was used, Streptavidin (HRP) ab7403 at a 1/10,000 dilution. DAB was used as the chromogen (ab103723), diluted 1/100 and incubated for 10 min at room temperature. The section was then counterstained with hematoxylin and mounted with DPX. The inset negative control image is taken from an identical assay without primary antibody.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre
ELISA results of purified ab6788 tested against purified Mouse IgG. Each well was coated in duplicate with 1.0 μg of Mouse IgG. The starting dilution of antibody was 5 μg/ml and the X-axis represents the Log 10 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 3% fish gelatin as blocking buffer, Streptavidin Peroxidase Conjugated and TMB substrate.
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