XRCC1 (Phospho Thr284) rabbit pAb

    • Catalog No.:YP1744
    • Applications:WB
    • Reactivity:Human;Mouse;Rat
      • Target:
      • XRCC1
      • Fields:
      • >>Base excision repair
      • Gene Name:
      • XRCC1
      • Protein Name:
      • XRCC1 (Phospho-Thr284)
      • Human Gene Id:
      • 7515
      • Human Swiss Prot No:
      • P18887
      • Mouse Swiss Prot No:
      • Q60596
      • Immunogen:
      • Synthesized peptide derived from human XRCC1 (Phospho-Thr284)
      • Specificity:
      • This antibody detects endogenous levels of XRCC1 (Phospho-Thr284) at Human, Mouse,Rat
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Polyclonal, Rabbit,IgG
      • Dilution:
      • WB 1:500-2000
      • Purification:
      • The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
      • Concentration:
      • 1 mg/ml
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • DNA repair protein XRCC1 (X-ray repair cross-complementing protein 1)
      • Molecular Weight(Da):
      • 70kD
      • Background:
      • The protein encoded by this gene is involved in the efficient repair of DNA single-strand breaks formed by exposure to ionizing radiation and alkylating agents. This protein interacts with DNA ligase III, polymerase beta and poly (ADP-ribose) polymerase to participate in the base excision repair pathway. It may play a role in DNA processing during meiogenesis and recombination in germ cells. A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity. [provided by RefSeq, Jul 2008],
      • Function:
      • function:Corrects defective DNA strand-break repair and sister chromatid exchange following treatment with ionizing radiation and alkylating agents.,polymorphism:Carriers of the polymorphic Gln-399 allele may be at greater risk for tobacco- and age-related DNA damage.,PTM:Phosphorylation of Ser-371 causes dimer dissociation. Phosphorylation by CK2 promotes interaction with APTX and APLF.,PTM:Sumoylated.,similarity:Contains 2 BRCT domains.,subcellular location:Accumulates at sites of DNA damage.,subunit:Homodimer. Interacts with polynucleotide kinase (PNK), DNA polymerase-beta (POLB) and DNA ligase III (LIG3). Interacts with APTX and APLF.,
      • Subcellular Location:
      • Nucleus . Moves from the nucleoli to the global nuclear chromatin upon DNA damage. .
      • Expression:
      • Expressed in fibroblasts, retinal pigmented epithelial cells and lymphoblastoid cells (at protein level).
      • Products Images
      • Western Blot analysis of 1 HeLa cell, 2 LPS 100ng/mL 30min treated ,using primary antibody at 1:1000 dilution. Secondary antibody(catalog#:RS23920) was diluted at 1:10000