FANCG (phospho Ser383) Polyclonal Antibody

Background:
Fanconi anemia complementation group G(FANCG) Homo sapiens 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. [provided by RefSeq, Jul 2008],

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

Immunogen: Synthesized phospho-peptide around the phosphorylation site of human FANCG (phospho Ser383)

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

Observed band: 69

GeneID: FANCG

Storage: -20°C/1 year

NOTE: For Research Use Only