Suitable for WB, IP, Flow Cyt, ICC/IF, IHC-Fr, ELISA, IHC-P. Cited in 2 publications.
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application WB | Reactivity Reacts | Dilution info - | Notes - |
Application IP | Reactivity Reacts | Dilution info - | Notes - |
Application Flow Cyt | Reactivity Reacts | Dilution info - | Notes - |
Application ICC/IF | Reactivity Reacts | Dilution info - | Notes - |
Application IHC-Fr | Reactivity Reacts | Dilution info - | Notes - |
Application ELISA | Reactivity Reacts | Dilution info 1/20000.00000 - 1/200000.00000 | Notes - |
Application IHC-P | Reactivity Reacts | Dilution info 1/500.00000 - 1/5000.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Igh-4, Ighg1, Ig gamma-1 chain C region secreted form
Suitable for WB, IP, Flow Cyt, ICC/IF, IHC-Fr, ELISA, IHC-P. Cited in 2 publications.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: PBS, 30% Glycerol (glycerin, glycerine), 1% BSA
Immunogen affinity purified - This antibody was isolated by affinity chromatography using antigen coupled to agarose beads and conjugated to Biotin.
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IHC image of Histone H4 staining in a section of formalin-fixed paraffin-embedded normal human colon tissue*. ab208001 Donkey Anti-Mouse IgG H & L (Biotin) was used as the secondary antibody.
Staining was performed on a Leica BondTM. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins, before blocking of endogenous biotin using Avidin/Biotin Blocking Kit ab64212. The section was then incubated with Anti-Histone H4 antibody [mAbcam 31830] - ChIP Grade ab31830, 1/100 dilution, for 15 mins at room temperature, followed by ab208001, 1/500 dilution, for 15 mins at room temperature. Detection was via an HRP conjugated ABC system and DAB was used as the chromogen. The section was then counterstained with haematoxylin 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
ab208001was tested by direct ELISA, where wells were coated with serially diluted mouse IgG (1000 – 16 ng/ml) for 2 hours, followed by a 2 hour blocking step (5% BSA). ab208001 (1:20,000 dilution; 2 hours) was added and detected by streptavidin-HRP (Streptavidin (HRP) ab7403; 1:10,000 dilution; 1 hour). Signal was developed by TMB substrate. Data from duplicates; +/- SD.
IHC image of alpha Tubulin staining in a section of formalin-fixed paraffin-embedded normal human colon tissue*. ab208001 Donkey Anti-Mouse IgG H & L (Biotin) was used as the secondary antibody.
Staining was performed on a Leica BondTM. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins, before blocking of endogenous biotin using Avidin/Biotin Blocking Kit ab64212. The section was then incubated with Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291, 1/100 dilution, for 15 mins at room temperature, followed by ab208001, 1/500 dilution, for 15 mins at room temperature. Detection was via an HRP conjugated ABC system and DAB was used as the chromogen. The section was then counterstained with haematoxylin 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
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