XRCC2 Polyclonal Antibody, 20ul Molecular Weight Markers Mutations in this gene are

Mutations in this gene are associated with isolated steroid-17 alpha-hydroxylase deficiency

is a multimeric protein composed of 3 alpha subunits

Among its related pathways are Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 and Bacterial invasion of epithelial cells

The upstream stimulatory factor 2 can activate transcription through pyrimidine-rich initiator (Inr) elements and E-box motifs and is involved in regulating multiple cellular processes

one of two putative serine/threonine kinases that become associated with the interleukin-1 receptor (IL1R) upon stimulation

XRCC2 Polyclonal Antibody, 20ul Molecular Weight Markers Mutations in this gene areXRCC2 encodes a member of the RecA Rad51 related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. This gene is involved in the repair of DNA double strand breaks by homologous recombination and it functionally complements Chinese hamster irs1, a repair deficient mutant that exhibits hypersensitivity to a number of different DNA damaging agents.