XPA Antibody

Mutations in XPA (xeroderma pigmentosum group A-complementing protein) are the cause of xeroderma pigmentosum A (XP-A), an autosomal recessive disease that is mainly characterized by a susceptibility to UV-induced skin cancer and in some cases neurological abnormalities. XPA is one of seven XP complementation groups that have been identified. The XP complementation groups represent genes critical to the nucleotide excision repair (NER) pathway. XPA is thought to function in the recognition of DNA damage and as a processivity factor for XPF and XPG.
XPA
XPA, DNA damage recognition and repair factor
DNA repair protein complementing XP-A cells
:  excision repair-controlling mutant xeroderma pigmentosum complementation group A xeroderma pigmentosum group A-complementing protein xeroderma pigmentosum, complementation group A XP1 XPAC
Product
Specifications
Ordering Information
Human
WB, IP, IHC
Between 1 and 50
$339
$229
$99
Human
IHC
Between 1 and 50
$360
$99