E-AB-11217
FANCG Polyclonal Antibody
Size
£106.20
Was £118.00
- SKU:
- E-AB-11217
- Additional Names:
- 9,DNA repair protein XRCC9,FAG,FANCG,Fanconi anaemia complementation group G,Fanconi anemia group G protein,Protein FACG,X ray repair,X-ray repair,XRCC9,complementing defective,in Chinese hamster,in Chinese hamster cells 9
- Application:
- IHC
- Concentration:
- 1 mg/ml
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Recombinant protein of human FANCG
- 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.
- Shipping Conditions:
- Blue Ice