FANCA Polyclonal Antibody | G-AB-11799

FANCA Polyclonal Antibody | G-AB-11799 | Gentaur Antibodies

Overview: 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 A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia.

Category Type: Polyclonal Antibody

Research Areas: Epigenetics and Nuclear Signaling

Synonyms: FANCA, FA, FA-H, FA1, FAA, FACA, FAH, FANCH

Reactivity: Human

Host: Rabbit

Isotype: IgG

Gene ID: 2175

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human FANCA (NP_000126.2) .

Clone #:

Conjugation: Unconjugated

Swissprot: O15360

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: IHC

Dilution: IHC 1:50-1:200

Storage: Store at -20°C. Avoid freeze / thaw cycles.

FANCA Polyclonal Antibody DataSheet