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RAD51C Antibody (Center)Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

Country
United States
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Ordering Information
Catalog # Size Availability Price  
AP14962c 0.1 mg 400 ul In Stock $ 255.00 Add to cart
AP14962c-ev20 Ev20 size 100 ul In Stock $ 95.00 Add to cart
  • Specification
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RAD51C Antibody (Center) - Product info

ApplicationWB
  • Applications Legend:
  • W=Western Blotting
  • IP=Immunoprecipitation
  • IHC-P=Immunohistochemistry (Paraffin)
  • IF-IC=Immunofluorescence (Immunocytochemistry)
  • F=Flow Cytometry
Primary AccessionO43502
Other AccessionNP_478123.1, NP_002867.1
ReactivityHuman
Concentration0.25 mg/ml
IsotypeRabbit Ig
Calculated MW42190 Da

RAD51C Antibody (Center) - Additional info

Gene ID 5889
Other Names
RAD51C; RAD51L2; DNA repair protein RAD51 homolog 3; RAD51 homolog C; RAD51-like protein 2
Target/Specificity
This RAD51C antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 168-198 amino acids from the Central region of human RAD51C.
Dilution
WB~~1:100~500
Format
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
RAD51C Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures.

RAD51C Antibody (Center) - Protein Information

Name RAD51C
Synonyms RAD51L2
Function
Essential for the homologous recombination (HR) pathway of DNA repair. Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks arising during DNA replication or induced by DNA-damaging agents. The RAD51B-RAD51C dimer exhibits single-stranded DNA-dependent ATPase activity. The BCDX2 complex binds single-stranded DNA, single-stranded gaps in duplex DNA and specifically to nicks in duplex DNA. Participates in branch migration and Holliday junction resolution and thus is important for processing HR intermediates late in the DNA repair process. Also has an early function in DNA repair in facilitating phosphorylation of the checkpoint kinase CHEK2 and thereby transduction of the damage signal, leading to cell cycle arrest and HR activation. Protects RAD51 from ubiquitin-mediated degradation that is enhanced following DNA damage. Plays a role in regulating mitochondrial DNA copy number under conditions of oxidative stress in the presence of RAD51 and XRCC3. Contributes to DNA cross-link resistance, sister chromatid cohesion and genomic stability. Involved in maintaining centrosome number in mitosis
Cellular Location
Nucleus. Cytoplasm. Cytoplasm, perinuclear region. Mitochondrion. Note=DNA damage induces an increase in nuclear levels. Accumulates in DNA damage induced nuclear foci or RAD51C foci which is formed during the S or G2 phase of cell cycle. Accumulation at DNA lesions requires the presence of NBN/NBS1, ATM and RPA
Tissue Location
Expressed in a variety of tissues, with highest expression in testis, heart muscle, spleen and prostate

RAD51C Antibody (Center) - Related products

AP14962c: RAD51C Antibody (Center)

AF1901a: RAD51C Antibody

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BACKGROUND

This gene is a member of the RAD51 family of related genes, which encode strand-transfer proteins thought to be involved in recombinational repair of damaged DNA and in meiotic recombination. This gene product interacts with two other DNA repair proteins, encoded by RAD51B and XRCC3, but not with itself. The protein copurifies with XRCC3 protein in a complex, reflecting their endogenous association and suggesting a cooperative role during recombinational repair. This gene is one of four localized to a region of chromosome 17q23 where amplification occurs frequently in breast tumors. Overexpression of the four genes during amplification has been observed and suggests a possible role in tumor progression. Alternative splicing has been observed for this gene and two variants encoding different isoforms have been identified.

REFERENCES

Zheng, Y., et al. Breast Cancer Res. Treat. (2010) In press : Briggs, F.B., et al. Am. J. Epidemiol. 172(2):217-224(2010) Monsees, G.M., et al. Breast Cancer Res. Treat. (2010) In press : Meindl, A., et al. Nat. Genet. 42(5):410-414(2010) Vaz, F., et al. Nat. Genet. 42(5):406-409(2010)