Rabbit Recombinant Monoclonal H2A phospho T120 antibody. Carrier free. Suitable for ELISA, WB, PepArr, IHC-P and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
ELISA | WB | PepArr | IHC-P | |
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Human | Tested | Tested | Tested | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling.
H2AFM, HIST1H2AB, H2AC8, H2AFA, HIST1H2AE, H2AC4, Histone H2A type 1-B/E, Histone H2A.2, Histone H2A/a, Histone H2A/m, H2AT120p
Rabbit Recombinant Monoclonal H2A phospho T120 antibody. Carrier free. Suitable for ELISA, WB, PepArr, IHC-P and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
ab249963 is the carrier-free version of Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 2% BSA/TBST.
This target is specifically expressed at M phase according to the literature (PMID: 19965387).
All lanes: Western blot - Anti-Histone H2A (phospho T120) antibody [EPR17492] (Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391) at 1/1000 dilution
Lane 1: Core histones purified by acid extraction precipitation from untreated HeLa (Human epithelial cell line from cervix adenocarcinoma) cells at 10 µg
Lane 2: Core histones purified by acid extraction precipitation from HeLa (Human epithelial cell line from cervix adenocarcinoma) cells treated with colcemid at 10 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Predicted band size: 14 kDa
Observed band size: 14 kDa
Exposure time: 1s
This data was developed using Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391, the same antibody clone in a different buffer formulation.
Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391 was tested in Peptide Array against 501 different modified and unmodified histone peptides; each peptide is printed on the array at six concentrations (each in triplicate).
Circle area represents affinity between the antibody and a peptide: all antigen-containing peptides are displayed as red circles, all other peptides as blue circles. The affinity is calculated as area under curve when antibody binding values are plotted against the corresponding peptide concentration. Each circle area is normalized to the peptide with the strongest affinity.
The complete dataset, including full list of all peptides and information on the position of each peptide in the diagram, is available under the Support & downloads section.
This data was developed using Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded human colon tissue labeling Histone H2A (phospho T120) with Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391 at 1/16000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Sporadically nuclear staining on human colon [PMID: 19965387]. Counter stained with Hematoxylin. Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
This data was developed using Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded human spleen tissue labeling Histone H2A (phospho T120) with Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391 at 1/16000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Sporadically nuclear staining on germinal center of human spleen [PMID: 19965387]. Counter stained with Hematoxylin. Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
This data was developed using Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded human gastric tumor tissue labeling Histone H2A (phospho T120) with Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391 at 1/16000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Sporadically nuclear staining on tumor cells of human gastric tumor [PMID: 19965387]. Counter stained with Hematoxylin. Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
This data was developed using Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391, the same antibody clone in a different buffer formulation.Direct ELISA analysis using Anti-Histone H2A (phospho T120) antibody [EPR17492] ab177391 (0 to 1000 ng/ml) in peptide ELISA with H2A T120 phospho peptide, H2A unmodified peptide, H2A.XT120 phospho peptide and H2A.X unmodified peptide as antigens (at 1000 ng/ml concentration). An Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution was used as secondary antibody.
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