FANCG (phospho Ser383) rabbit pAb - ES5203

FANCG (phospho Ser383) rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES5203-50, ES5203-100

Citations, Manuals and MSDS Available upon request.

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. [provided by RefSeq, Jul 2008],

Alternate Name: FANCG; XRCC9; Fanconi anemia group G protein; Protein FACG; DNA repair protein XRCC9

Source: Rabbit

Applications: WB; ELISA

Dilution: Western Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.

Reactivity: Human; Rat; Mouse;

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

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Observed Band (KD): 69kD

Human Gene ID: 2189

Human SWISS Prot NO: O15287

Subcellular Location: Nucleus. Cytoplasm. The major form is nuclear. The minor form is cytoplasmic.

Research Use Only