epitope corresponding to amino acids 641-940 mapping at the C-terminus of XPC of human origin
recommended for detection of XPC of mouse, rat and human origin by WB, IP, IF, IHC(P) and ELISA; also reactive with additional species, including canine, bovine and porcine
XPC Background Information Xeroderma pigmentosum (XP) is an autosomal recessive disorder characterized by a genetic predisposition to sunlight-induced skin cancer due to deficiencies in the DNA repair enzymes. The most frequent mutations are found in the XP genes of group A through G and group V, which encode nucleotide excision repair (NER) proteins. NER provides versatile DNA repair mechanisms to en-sure the proper functioning of all cells. The majority of patients with XP carry mutations in either the XPA or XPC genes, which encode proteins involved in the recognition of damaged DNA. The gene encoding human XPC maps to chromosome 3p25. XPC forms a complex with Cen2 and the human homolog of yeast Rad23B (HR23B), both of which stabilize XPC; it also excises thymine dimers from damaged DNA. Specifically, the carboxy-terminus of XPC is re-quired for HR23B and DNA binding and, subsequently, mutations leading to carboxy-terminal truncations result in nonfunctional XPC proteins.
XPC (H-300) 논문정보
XPC (H-300): sc-30156 antibody 및 XPC (H-300) antibody conjugates를 사용한 논문들을 보세요.
5 total citations
논문 자료 로드 중입니다.
XPC (H-300)
클릭하시면 확대된 이미지를 보실 수 있습니다.
XPC (H-300): sc-30156. Western blot analysis of XPC expression in Hs68 whole cell lysate.
XPC (H-300): sc-30156. Immunofluorescence staining of methanol-fixed HeLa cells showing nuclear localization.
XPC (H-300): sc-30156. Immunoperoxidase staining of formalin fixed, paraffin-embedded human fallopian tube tissue showing nuclear staining of glandular cells at low (A) and high (B) magnification. Kindly provided by The Swedish Human Protein Atlas (HPA) program.
