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Products:Epigenetics and Nuclear Signaling >> Histones >> H3 >> Acetyl + Phospho
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Read our guarantee »Anti-Histone H3 (phospho S10, acetyl K9) antibody [APH3-64]
See all Histone H3 products (2) ...
Mouse monoclonal [APH3-64] to Histone H3 (phospho S10, acetyl K9)
Staining of (acetyl K9) & (phospho S10) histone H3 in immunoblotting is specifically inhibited with the immunizing peptide. There is no inhibition with non-acetylated histone H3 peptide or with singly modified (acetyl K9) or (phospho S10) histone H3 peptide.
WB, ELISA, IPmore details
Reacts with
Human
Predicted to work with
Mouse, Rat, Chicken, Cow, Xenopus laevis, Caenorhabditis elegans, Fruit fly (Drosophila melanogaster), a wide range of other species
A synthetic, acetylated and phosphorylated histone H3 peptide (amino acids 7-20, acetyl K9 & phospho S10) corresponding to the N-terminus of human histone H3, conjugated to KLH.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 15mM Sodium Azide
Constituents: 0.01M PBS
Concentration information loading...
Immunogen affinity purified
Whole antiserum is fractionated and then further purified by ion-exchange chromatography. The resulting IgG fraction is further purified by absorption on the unmodified histone H3 peptide (human, amino acids 7-20).
Monoclonal
APH3-64
NS1
IgG2a
Epigenetics and Nuclear Signaling >> Histones >> H3 >> Acetyl + Phospho
Our Abpromise guarantee covers the use of ab12180 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ELISA: Use at an assay dependent dilution.
IP: Use at an assay dependent dilution.
WB: Use at a concentration of 1 - 2 µg/ml. Detects a band of approximately 17 kDa.
Not tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
We advise you to centrifuge this product vial before use.
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fibre is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. Covalent modifications of the canonical core histones, including acetylation, phosphorylation, methylation, and monoubiquitination, are used to mark nucleosomes to create chromatin domains with a range of functions. The information encoded by the modifications can contribute to the formation and/or maintenance of transcriptionally active and inactive chromatin in response to various signalling pathways. Phosphorylation, particularly that of histones H1 and H3, has long been implicated in chromosome condensation during mitosis. However, converging evidence suggests that H3 phosphorylation (specifically serine 10) is also directly correlated with the induction of immediate-early genes such as c-jun, c-fos and c-myc. The potential importance of the serine 10 phosphorylation mark in H3 is strengthened by the finding that MSK1, a kinase activated by growth factor and stress stimuli, also phosphorylates H3 in vitro. H3 phosphorylation at serine 10 in conjunction with phosphorylation at serine 28, is also required for proper segregation and condensation of chromosomes during mitosis and meiosis.
ab12180 has not yet been referenced specifically in any publications.
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