Goat anti-mouse IgG H&L (HRP) is a secondary antibody for chemiluminescent detection. Ideal for western blot. Suitable for ICC, IHC, western blot and more.
- Cited in over 1580 publications
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application IP | Reactivity Reacts | Dilution info - | Notes - |
Application Dot | Reactivity Expected | Dilution info - | Notes - |
Application IM | Reactivity Expected | Dilution info - | Notes - |
Application IHC-Fr | Reactivity Expected | Dilution info 1/500 - 1/2500 | Notes - |
Application WB | Reactivity Reacts | Dilution info 1/2000 - 1/10000 | Notes - |
Application IHC-P | Reactivity Reacts | Dilution info 1/500 - 1/2500 | Notes - |
Application ELISA | Reactivity Reacts | Dilution info 1/100000 | Notes - |
Application ICC | Reactivity Expected | Dilution info 1/500 - 1/2500 | Notes - |
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Igh-4, Ighg1, Ig gamma-1 chain C region secreted form
Goat anti-mouse IgG H&L (HRP) is a secondary antibody for chemiluminescent detection. Ideal for western blot. Suitable for ICC, IHC, western blot and more.
- Cited in over 1580 publications
pH: 7.2
Preservative: 0.01% Gentamicin sulphate
Constituents: 1% BSA, 0.88% Sodium chloride, 0.424% Potassium phosphate solution
MOUSE IgG (H&L) Antibody Peroxidase Conjugated was prepared from monospecific antiserum by immunoaffinity chromatography using Mouse IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities.
The product can contain small precipitates giving a cloudy appearance. However this does not affect the performace of the product. Leaving the product at room temperature in the dark for a few hours may help. Please use as normal and if you do experience problems, contact Scientific Support.
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Terms & Conditions.
All lanes: Western blot - Anti-GAPDH antibody [mAbcam 9484] - Loading Control (Anti-GAPDH antibody [mAbcam 9484] - Loading Control ab9484) at 0.5 µg/mL
All lanes: HeLa cell lysate
All lanes: Western blot - Goat Anti-Mouse IgG H&L (HRP) (ab6789) at 1/5000 dilution
Developed using the ECL technique.
Performed under non-reducing conditions.
Predicted band size: 36 kDa
Exposure time: 30s
Anti-HA tag antibody [HA-7] ab49969 Immunoprecipitating HA Tag in HEK-293T whole cell lysate. 25 μg of cell lysate was incubated with primary antibody (1/2500 in lysis buffer) and matrix (Protein A/G) for 6 hours at 4°C. For western blotting a HRP-conjugated goat anti-mouse IgG H&L (ab6789) (1/1000) was used to confirm successful immunoprecipation.
All lanes: Immunoprecipitation - Goat Anti-Mouse IgG H&L (HRP) (ab6789)
All lanes: Anti-CDC42 Binding Protein Kinase Beta antibody (ab61328) at 1/2000 dilution
All lanes: Cytosolic fraction prepared from murine brain tissue at 10 µg
All lanes: Western blot - Goat Anti-Mouse IgG H&L (HRP) (ab6789) at 1/2000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Exposure time: 1min
IHC image of beta actin staining in human colon formalin fixed paraffin embedded tissue section*.
The section was pre-treated using pressure cooker heat mediated antigen retrieval with sodium citrate buffer (pH 6) for 30 mins. The section was incubated with Anti-beta Actin antibody [mAbcam 8224] - Loading Control ab8224, 3 μg/ml overnight at +4°C. An HRP-conjugated secondary (ab6789, 1/2000 dilution) was used for 1hr at room temperature. The section was counterstained with hematoxylin and mounted with DPX.
The inset negative control image is secondary-only at 1/500 dilution.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre
Western blot analysis of ab6789 used as a secondary antibody at 1/1000 dilution for 60 min at RT.
All lanes: Mouse IgG at 50 ng
All lanes: Western blot - Goat Anti-Mouse IgG H&L (HRP) (ab6789) at 1/1000 dilution
ELISA results of ab6789 against purified Mouse IgG protein. Each well was coated in duplicate with 10 µg of Mouse IgG. The starting dilution of antibody was 5 µg/ml and the X-axis represents the Log10 of a 3-fold dilution. The titer is 1/106,000. 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 and TMB substrate.
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