• Immunohistochemistry of paraffin-embedded rat liver using Phospho-Histone H2A-S129 antibody (STJ11101101) at dilution of 1:100 (40x lens).
  • Immunohistochemistry analysis of Phospho-Histone H2A-S129 in paraffin-embedded human breast cancer using Phospho-Histone H2A-S129 Rabbit polyclonal antibody (STJ11101101) at dilution of 1:100 (40x lens). Perform microwave antigen retrieval with 10 mM Tris/EDTA buffer pH 9. 0 before commencing with immunohistochemistry staining protocol.
  • Immunohistochemistry of paraffin-embedded human breast cancer using Phospho-Histone H2A-S129 antibody (STJ11101101) at dilution of 1:100 (40x lens).
  • Immunohistochemistry analysis of Phospho-Histone H2A-S129 in paraffin-embedded rat liver using Phospho-Histone H2A-S129 Rabbit polyclonal antibody (STJ11101101) at dilution of 1:100 (40x lens). Perform microwave antigen retrieval with 10 mM Tris/EDTA buffer pH 9. 0 before commencing with immunohistochemistry staining protocol.

Anti-Phospho-Histone H2A-S129 antibody (STJ11101101)

SKU:
STJ11101101

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Host: Rabbit
Applications: IHC
Reactivity: Human/Rat
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Rabbit polyclonal antibody anti-Phospho-Histone H2A-S129 is suitable for use in Immunohistochemistry research applications.
Clonality: Polyclonal
Conjugation: Unconjugated
Isotype: IgG
Formulation: PBS with 0.01% Thimerosal, 50% Glycerol, pH7.3.
Purification: Affinity purification
Dilution Range: IHC-P 1:50-1:200
Storage Instruction: Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.
Immunogen: A synthetic phosphorylated peptide around S129 of saccharomyces cerevisiae Histone H2A (NP_010511.3?).
Immunogen Sequence: KASQE
Background This gene encodes a single-strand specific DNA endonuclease that makes the 3 incision in DNA excision repair following UV-induced damage. The protein may also function in other cellular processes, including RNA polymerase II transcription, and transcription-coupled DNA repair. Mutations in this gene cause xeroderma pigmentosum complementation group G (XP-G) , which is also referred to as xeroderma pigmentosum VII (XP7) , a skin disorder characterized by hypersensitivity to UV light and increased susceptibility for skin cancer development following UV exposure. Some patients also develop Cockayne syndrome, which is characterized by severe growth defects, cognitive disability, and cachexia. Read-through transcription exists between this gene and the neighboring upstream BIVM (basic, immunoglobulin-like variable motif containing) gene.

Information sourced from Uniprot.org

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