Suitable for IP, Dot, IM, IHC-Fr, WB, IHC-P, ELISA, ICC. Ideal for western blot. Cited in 1583 publications.
Goat
Mouse
IgG
Heavy & Light chains
HRP
IP, Dot, IM, IHC-Fr, WB, IHC-P, ELISA, ICC
Polyclonal
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application IP | Reactivity Reacts | Dilution info - | Notes - |
Application Dot | Reactivity Reacts | Dilution info - | Notes - |
Application IM | Reactivity Reacts | Dilution info - | Notes - |
Application IHC-Fr | Reactivity Reacts | 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 Reacts | Dilution info 1/500 - 1/2500 | Notes - |
Select an associated product type
Ig gamma-1 chain C region, membrane-bound form
Ig gamma-1 chain C region secreted form, Ighg1, Igh-4
Suitable for IP, Dot, IM, IHC-Fr, WB, IHC-P, ELISA, ICC. Ideal for western blot. Cited in 1583 publications.
Ig gamma-1 chain C region secreted form, Ighg1, Igh-4
Goat Anti-Mouse IgG H&L (HRP)
Goat
Mouse
IgG
Heavy & Light chains
HRP
IP, Dot, IM, IHC-Fr, WB, IHC-P, ELISA, ICC
Polyclonal
No
IgG
Liquid
Preservative: 0.01% Gentamicin sulphate
Constituents: 1% BSA, 0.878% Sodium chloride, 0.424% Tripotassium orthophosphate
Affinity purification
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.
Blue Ice
+4°C
Store in the dark
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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Full details and terms and conditions can be found here:
Terms & Conditions.
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: 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.
Predicted band size: 36 kDa
Exposure time: 30s
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
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