FANCG / XRCC9 polyclonal, anti-human

Background:
The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group G.

Other Names:
Fanconi anemia group G protein, Protein FACG, DNA repair protein XRCC9, FANCG, XRCC9

Antigen Types:
Synthetic Peptide

Gene Name:
FANCG
Gene ID:
2189
Primary Accession: O15287
Other Accession: NP_004620;2189;