FANCC Rabbit Polyclonal Antibody

CAT#: TA319294

Rabbit polyclonal anti-FANCC antibody

Product Images

WB using Anti-FANCC antibody shows detection of a band at ~63 kDa (arrowhead) corresponding to FANCC present in a HeLa whole cell lysate. The identity of the lower molecular weight band is unknown. The primary antibody was diluted to 1:1, 500. IRDye™800 conjugated Gt-a-Rabbit IgG [H&L] was used at 1:10,000. Molecular weight estimation was made by comparison to prestained MW markers (indicated at left).

Specifications

Product Data

• Applications: WB
• Recommended Dilution: ELISA: 1:20,000 - 1:80,000, WB: 1:1,000 - 1:3,000
• Reactivities: Chimpanzee, Human
• Host: Rabbit
• Isotype: IgG
• Clonality: Polyclonal
• Immunogen: This affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to amino acids 96-112 of Human FANCC.
• Formulation: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
• Concentration: lot specific
• Conjugation: Unconjugated
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Gene Name: Fanconi anemia complementation group C
• Database Link:
  NP_000127
  Entrez Gene 2176 Human
  UniProt ID Q00597
• Synonyms: FA3; FAC; FACC
• Note: FANCC (also called Protein FACC or Fanconi Anemia Group C protein) is involved in DNA repair, perhaps specifically with post-replication repair or a cell cycle checkpoint function. FANCC may also be implicated in interstrand DNA cross-link repair and in the maintenance of normal chromosome stability. FANCC belongs to the multi-subunit Fanconi Anemia (FA) complex composed of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL/PHF9 and FANCM. FANCC is mainly found within the nucleus although some protein is localized in the cytoplasm. This protein is ubiquitously expressed. Defects in FANCC are a cause of Fanconi anemia (FA). FA is a genetically heterogeneous, autosomal recessive disorder characterized by progressive pancytopaenia, a diverse assortment of congenital malformations, and

Reference Data

• Protein Families: Druggable Genome