ANTIBODIES

Contributor Information
- Name Michael Tilby
- Institute The Institute of Cancer Research; Newcastle University
Tool Details
- Tool name: Anti-Cisplatin modified DNA [CP9/19]
- Clone: CP9/19
- Tool type: Antibodies
- Tool sub-type: Primary antibody
- Class: Monoclonal
- Conjugate: Unconjugated
- Host: Rat
- Cancer type: Chemotherapy; Broadly Applicable
- Application: ELISA ; FACS ; IHC ; IP ; DB
- Description: Antibody CP9/19 recognises only the intra-strand cross-links formed by cisplatin between adjacent purines.
- Immunogen: Cisplatin modified native DNA
- Isotype: IgG2a
- Research area: Genetics
- Myeloma used: Y3.AG.1.2.3
- For Research Use Only
Target Details
- Target: Cisplatin modified native DNA
- Target background: This antibody enables the quantification of cisplatin-induced adducts on DNA. This antibody has also been recently used for isolation of DNA fragments carrying adducts to enhance the sensitivity of subsequent PCR-based analyses and is central to ongoing studies of variation in the nature of cisplatin adducts formed in different cell lines.
Application Details
- Application: ELISA ; FACS ; IHC ; IP ; DB
Handling
- Format: Liquid
- Concentration: 1 mg/ml
- Storage buffer: PBS with 0.02% azide
- Storage conditions: -15ðC to -25ðC
- Shipping conditions: Shipping at 4ðC
Related Tools
References
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- • 3D-DIP-Chip: a microarray-based method to measure genomic DNA damage.
- • Kothandapani et al. 2012. Exp Cell Res. 318(16):1973-86. PMID: 22721696.
- • Downregulation of SWI/SNF chromatin remodeling factor subunits modulates cisplatin cytotoxicity.
- • Kothandapani et al. 2011. J Biol Chem. 286(16):14564-74. PMID: 21357694.
- • Novel role of base excision repair in mediating cisplatin cytotoxicity.
- • Meczes et al. 2005. Biochem Pharmacol. 70(12):1717-25. PMID: 16259963.
- • Specific adducts recognised by a monoclonal antibody against cisplatin-modified DNA.
- • Deverman et al. 2002. Cell. 111(1):51-62. PMID: 12372300.
- • Bcl-xL deamidation is a critical switch in the regulation of the response to DNA damage.
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- • Veal et al. 2001. Clin Cancer Res. 7(8):2205-12. PMID: 11489793.
- • Influence of cellular factors and pharmacokinetics on the formation of platinum-DNA adducts in leukocytes of children receiving cisplatin therapy.
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- • BRG-1 is required for RB-mediated cell cycle arrest.
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- • Pharmacokinetically guided dose escalation of carboplatin in epithelial ovarian cancer: effect on drug-plasma AUC and peripheral blood drug-DNA adduct levels.
- • Welters et al. 1999. Ann Oncol. 10(1):97-103. PMID: 10076728.
- • The potential of plantinum-DNA adduct determination in ex vivo treated tumor fragments for the prediction of sensitivity to cisplatin chemotherapy.
- • Peng et al. 1997. Br J Cancer. 76(11):1466-73. PMID: 9400943.
- • Platinum-DNA adduct formation in leucocytes of children in relation to pharmacokinetics after cisplatin and carboplatin therapy.
- • Cross et al. 1996. Int J Cancer. 66(3):404-8. PMID: 8621265.
- • Effect of quercetin on the genotoxic potential of cisplatin.
- • Evans et al. 1994. Cancer Res. 54(6):1596-603. PMID: 8137265.
- • Differential sensitivity to the induction of apoptosis by cisplatin in proliferating and quiescent immature rat thymocytes is independent of the levels of drug accumulation and DNA adduct formation.
- • Tilby et al. 1991. Cancer Res. 51(1):123-9. PMID: 1703029.
- • Sensitive detection of DNA modifications induced by cisplatin and carboplatin in vitro and in vivo using a monoclonal antibody.