|Full Name||Fanconi anemia, complementation group G|
|Product Description||Rabbit Polyclonal antibody to FANCG (Fanconi anemia, complementation group G)|
|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]|
|Synonyms||FAG antibody, XRCC9 antibody, FANCG antibody, DNA repair protein XRCC9 antibody, Fanconi anemia group G protein antibody, X-ray repair complementing defective repair in Chinese hamster cells 9 antibody, "X-ray repair, complementing defective, in Chinese hamster, 9 antibody", "Fanconi anemia, complementation group G antibody"|
|Immunogen||Recombinant protein encompassing a sequence within the center region of human FANCG. The exact sequence is proprietary.|
|Species Reactivity||Human, Mouse|
|Predicted Cross Reactivity species Predicted cross-reactivity:|
Predicted cross-reactivity is based on sequence homology, with greater than 80% immunogen sequence identity considered positive.
Please note that we are only able to guarantee products to work in applications and species in which they have been tested.
|Predict Reactivity Note||Rhesus Monkey (95%)|