Xeroderma Pigmentosum, Complementation Group G (XPG)
XP-G; ERCM2; ERCC5; UVDR; XPGC; Excision Repair Cross-Complementing Rodent Repair Deficiency,Complementation Group 5; Cockayne Syndrome
 HGNC 3437
 MGI 103582
 PubMed 22417308
 RGD 1586176
 UniProt P28715
 USCN B871
 Wiki ERCC5
Xeroderma Pigmentosum, Complementation Group G (XPG)
ERCC5  is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined.
The human genes correcting DNA repair defects are termed excision-repair cross-complementing or ERCC genes. A number appended to the symbol refers to the rodent complementary group that is corrected by the human gene. The ERCC5 gene corrects the excision repair deficiency of Chinese hamster ovary cell line UV135 of complementation group 5.
Organism species: Homo sapiens (Human)
CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins RPB871Hu01 Recombinant Xeroderma Pigmentosum, Complementation Group G (XPG) SDS-PAGE; WB; ELISA; IP.
Antibodies MAB871Hu22 Monoclonal Antibody to Xeroderma Pigmentosum, Complementation Group G (XPG) WB, ICC, IHC-P, IHC-F, ELISA
PAB871Hu01 Polyclonal Antibody to Xeroderma Pigmentosum, Complementation Group G (XPG) WB, ICC, IHC-P, IHC-F, ELISA
Assay Kits SEB871Hu ELISA Kit for Xeroderma Pigmentosum, Complementation Group G (XPG) Enzyme-linked immunosorbent assay
SCB871Hu CLIA Kit for Xeroderma Pigmentosum, Complementation Group G (XPG) Chemiluminescent immunoassay
Organism species: Mus musculus (Mouse)
CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a n/a n/a
Antibodies n/a n/a n/a
Assay Kits n/a n/a n/a
Organism species: Rattus norvegicus (Rat)
CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a n/a n/a
Antibodies n/a n/a n/a
Assay Kits n/a n/a n/a