FANCG antibody [N1N3]

Cannot supply to this region.

SKU:: GTX100164
Additional Names:: FA complementation group G , FAG , XRCC9
Application:: WB, IF, ICC
Concentration:: 1 mg/ml
Physical State:: Liquid
Species Reactivity:: Human
Purification:: Affinity Purified
Storage Conditions:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:: Genetex
Host:: Rabbit
Reactivities:: Human, Mouse
Buffer:: PBS, 40% Glycerol, 0.01% Thimerosal.
Immunogen:: Recombinant protein encompassing a sequence within the center region of human FANCG. The exact sequence is proprietary.
Clone:: N1N3
Uniprot:: O15287
Synonyms:: DNA repair protein XRCC9;FAG;Fanconi anemia complementation group G;Fanconi anemia group G protein;truncated Fanconi anemia group G protein;X-ray repair complementing defective repair in Chinese hamster cells 9;X-ray repair, complementing defective, in Chinese hamster, 9;XRCC9
Extra Details:: 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]

Shipping Conditions:: Blue Ice