Recommended positive controls: 293T, A431, HeLa, HepG2, NIH-3T3.
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
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 C.
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
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Protein Aliases: FA3; FAC; FACC; Fanconi anemia group C protein; Fanconi anemia group C protein homolog; Fanconi anemia, complementation group C; Protein FACC; RP11-80I15.2
Gene Aliases: FA3; FAC; FACC; FANCC; mir-3074-1