- Antibody Type
- Recombinant monoclonal
- Target
- Phospho-Histone H2B (Ser14)
- Reactivity
- Human
- Application
- WB
- MW(Calculated)
- 14 kDa
- MW(Observed)
- 15 kDa
- Host Species
- Rabbit
- Isotype
- IgG
- Conjugate
- Unconjugated
- Modification
- Phosphorylation
- Modification Site
- Ser14
- Recommended dilution ratio
- WB 1:1000
- Composition
- PBS, Glycerol, BSA
- Purification process
- Protein A affinity purification
- storageCondition
- Store at -20°C. Avoid repeated freeze-thaw cycles
- Stability
- Stable for 12 months from date of receipt / reconstitution.
- Concentration
- --
- Clonal
- Recombinant monoclonal
- Clone Number
- W-R47
- Immunogen
- polypeptide
- Gene Name
- HIST1H2BK
- Protein Name
- Histone H2B
- Alternative name
- H2B, H2BS14ph
- Organism-1
- Human
- Gene ID
- 127797
- SwissProt-1
- P62807
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- Background:
- Background
- Histone post-translational modifications (PTMs) are key mechanisms of epigenetics that modulate chromatin structures, termed as “histone code”. The PTMs on histone including acetylation, methylation, phosphorylation and novel acylation directly affect the accessibility of chromatin to transcription factors and other epigenetic regulators, altering genome stability, gene transcription, etc. Histone phosphorylation occurs on serine, threonine and tyrosine residues on the aminoterminal of core histones. This histone mark plays roles in DNA repair, transcription and chromatin remodeling. The best-known histone phosphorylation site is histone variant H2A.x Ser139ph, which were reported to be involved in the response to DNA damage. Histone phosphorylation is mainly involved in processes during both mitosis and meiosis. Many kinases and phosphatases regulate histone phosphorylation levels.
- Cellular Localization
- Cytoplasm, Nucleus, Mitochondrion matrix, Mitochondrion outer membrane
- --
- Background:Histone post-translational modifications (PTMs) are key mechanisms of epigenetics that modulate chromatin structures, termed as “histone code”. The PTMs on histone including acetylation, methylation, phosphorylation and novel acylation directly affect the accessibility of chromatin to transcription factors and other epigenetic regulators, altering genome stability, gene transcription, etc. Histone phosphorylation occurs on serine, threonine and tyrosine residues on the aminoterminal of core histones. This histone mark plays roles in DNA repair, transcription and chromatin remodeling. The best-known histone phosphorylation site is histone variant H2A.x Ser139ph, which were reported to be involved in the response to DNA damage. Histone phosphorylation is mainly involved in processes during both mitosis and meiosis. Many kinases and phosphatases regulate histone phosphorylation levels.
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