ANTIBODIES

Contributor Information
- Name Dawn Batty ; Rick Wood
- Institute Cancer Research UK, London Research Institute: Lincoln's Inn Fields
Tool Details
- Tool name: Anti-XPC [RW028]
- Clone: RW028
- Tool type: Antibodies
- Tool sub-type: Primary antibody
- Class: Polyclonal
- Conjugate: Unconjugated
- Reactivity: Human
- Host: Rabbit
- Application: IF ; IF ; WB
- Description: Involved in global genome nucleotide excision repair (GG-NER) by acting as damage sensing and DNA-binding factor component of the XPC complex. Has only a low DNA repair activity by itself which is stimulated by RAD23B and RAD23A. Has a preference to bind DNA containing a short single-stranded segment but not to damaged oligonucleotides. This feature is proposed to be related to a dynamic sensor function: XPC can rapidly screen duplex DNA for non-hydrogen-bonded bases by forming a transient nucleoprotein intermediate complex which matures into a stable recognition complex through an intrinsic single-stranded DNA-binding activity.
- Immunogen: 96-299 of human XPC protein
- Research area: Genetics
- For Research Use Only
Target Details
- Target: Xeroderma Pigmentosum Group C (XPC)
- Target background: Involved in global genome nucleotide excision repair (GG-NER) by acting as damage sensing and DNA-binding factor component of the XPC complex. Has only a low DNA repair activity by itself which is stimulated by RAD23B and RAD23A. Has a preference to bind DNA containing a short single-stranded segment but not to damaged oligonucleotides. This feature is proposed to be related to a dynamic sensor function: XPC can rapidly screen duplex DNA for non-hydrogen-bonded bases by forming a transient nucleoprotein intermediate complex which matures into a stable recognition complex through an intrinsic single-stranded DNA-binding activity.
Application Details
- Application: IF ; IF ; WB
Handling
- Format: Liquid
- Shipping conditions: Shipping at 4ðC
Related Tools
References
- • HCMV-infected cells maintain efficient nucleotide excision repair of the viral genome while abrogating repair of the host genome.
- • O'Dowd et al. 2012. PLoS Pathog. 8(11):e1003038. PMID: 23209410.
- • O'Dowd et al. 2012. PLoS Pathog. 8(11):e1003038. PMID: 23209410.
- • Lange et al. 2009. DNA Repair (Amst). 8(7):865-72. PMID: 19446504.
- • Human HMGB1 directly facilitates interactions between nucleotide excision repair proteins on triplex-directed psoralen interstrand crosslinks.
- • Louat et al. 2004. FEBS Lett. 574(1-3):121-5. PMID: 15358551.
- • Atypical protein kinase C stimulates nucleotide excision repair activity.
- • Ara
jo et al. 2001. Mol Cell Biol. 21(7):2281-91. PMID: 11259578. - • Strong Fn interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome.
- • Batty et al. 2000. J Mol Biol. 300(2):275-90. PMID: 10873465.
- • Stable binding of human XPC complex to irradiated DNA confers strong discrimination for damaged sites.
- • K
berle et al. 1999. Curr Biol. 9(5):273-6. PMID: 10074455. - • Defective repair of cisplatin-induced DNA damage caused by reduced XPA protein in testicular germ cell tumours.