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.
仕様
Synonyms：DNA repair protein XRCC9,FAG,FANCG,FANCG,Fanconi anaemia complementation group G,Fanconi anemia group G protein,Protein FACG,X ray repair,complementing defective,in Chinese hamster cells 9,X-ray repair,complementing defective,in Chinese hamster,9,XRCC9
Host：Rabbit
Reactivity：Human
Applications：IHC,ELISA
Concentration：1mg/mL
Immunogen：Recombinant protein of human FANCG
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：PBS with 0.05％ sodium azide, 50％ glycerol, PH7.3
