1) Studies on homologous recombination in mammals including human 2) Studies on the interaction of Rad51 protein with various proteins 3) To be used as a standard for Western blotting
限制
仅限研究用
状态
Liquid
浓度
1.0 mg/mL
缓冲液
20 mM Tris-HCl pH 8.0, 100 mM KCl, 1 mM DTT, 0.5 mM EDTA, 10 % glycerol
储存液
Dithiothreitol (DTT)
注意事项
This product contains Dithiothreitol (DTT): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
储存条件
-20 °C/-80 °C
储存方法
Store at -80 C for long period.
Murayama, Kurokawa, Mayanagi, Iwasaki: "Formation and branch migration of Holliday junctions mediated by eukaryotic recombinases." in: Nature, Vol. 451, Issue 7181, pp. 1018-21, (2008) (PubMed).
Kurumizaka, Aihara, Kagawa, Shibata, Yokoyama: "Human Rad51 amino acid residues required for Rad52 binding." in: Journal of molecular biology, Vol. 291, Issue 3, pp. 537-48, (1999) (PubMed).
Human Rad51 protein is a functional and structural homolog of E. coli RecA protein, which plays a major role in genetic recombination and recombination repair by mediating strand exchange reaction between homologous DNA strands. Rad51 functionally and physically interacts with its paralogs Dmc1, Rad51B, Rad51C, Rad51D, Xrcc2 and Xrcc3, and also with Rad52 in recombination processes. It also interacts with oncogene proteins and tumor suppressors such as BRCA1, BRCA2, and P53 for the maintenance of genome stability. Rad51 protein was highly purified from E. coli over-expressing human Rad51 protein as a recombinant protein. Since the tag was removed from the recombinant protein (it still contains Gly-Ser-His at the N-terminal), it has been shown to retain nuclear filament forming and strand-exchange activity as well as interaction with Rad52.