Independent Antibodies: Western Blot: XPC Antibody [NB100-58801] - Detection of Human XPC on HeLa whole cell lysate using NB100-58801. XPC was also immunoprecipitated by rabbit anti-XPC antibody NB100-58800.
The immunogen recognized by this antibody maps to a region between residue 890 and 940 of human xeroderma pigmentosum, complementation group C using the numbering given in entry NP_004619.2 (GeneID 7508).
Xeroderma pigmentosum group C-complementing protein
xeroderma pigmentosum, complementation group C
XP3
XPCCDNA repair protein complementing XP-C cells
Background
Human XPC (Xeroderma pigmentosum group C) is a member of a family of proteins that has been shown to be involved in the repair of DNA via the nucleotide excision repair (NER) pathway. Specifically, XPC is believed to be a part of a heteromeric protein complex that is involved in the recognition of the DNA lesions during global genomic repair but not transcription-coupled repair. XPC may play a part in DNA damage recognition and/or in altering chromatin structure to allow access by damage processing enzymes. Defects in XPC are a cause of xeroderma pigmentosum complementation group C (XPC); also known as xeroderma pigmentosum III (XP3). XPC is a rare human autosomal recessive disease characterized by solar sensitivity, high predisposition for developing cancers on areas exposed to sunlight and, in some cases, neurological abnormalities.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
van der Weegen Y, Berman HG, Mevissen TET, Apelt K The sequential and cooperative action of CSB, CSA and UVSSA targets the TFIIH complex to DNA damage-stalled RNA polymerase II bioRxiv (WB, Human)
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