XPG Antibody

Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) 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.

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.

We have publications tested in 1 confirmed species: Human.

We have publications tested in 2 applications: ICC/IF, WB.

Showing Publications 1 - 5 of 5.

Publications using NB100-74611	Applications	Species
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)	WB	Human
Stefos GC, Szantai E, Konstantopoulos D et al. aniFOUND: analysing the associated proteome and genomic landscape of the repaired nascent non-replicative chromatin Nucleic acids research 2021-03-08 [PMID: 33693861] (ICC/IF, Human)	ICC/IF	Human
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 Nat Commun 2020-11-07 [PMID: 33159085]
Tillhon M, Cazzalini O, Nardo T et al. p300/CBP acetyl transferases interact with and acetylate the nucleotide excision repair factor XPG. DNA Repair (Amst) 2012-10-01 [PMID: 22954786]
Wang QE, Han C, Milum K et al. Stem cell protein Piwil2 modulates chromatin modifications upon cisplatin treatment. Mutat Res 2011-03-01 [PMID: 21310163]

Array NB100-74611

• XPG Antibodies
• XPG ELISA Kits
• XPG Lysate
• XPG Proteins