Copyright
©The Author(s) 2005.
World J Gastroenterol. Nov 14, 2005; 11(42): 6694-6700
Published online Nov 14, 2005. doi: 10.3748/wjg.v11.i42.6694
Published online Nov 14, 2005. doi: 10.3748/wjg.v11.i42.6694
Figure 1 Representative gel shift experiments on nuclear (A) and cytoplasmic (B) extracts from human colon tissues.
Panel A: Normal (n) and pathologic (t) nuclear extracts, obtained from four colorectal cancer (K1-K4) and five adenoma (A1-A5) patients, were analyzed by EMSA as described in "Materials and methods". The positions of Ku band-shifts and of the free probe (FP) are indicated. The binding activity in nuclear extracts from the CaCo-2 cell line (CaCo) has been used as a standard in order to compare the activity in the different gels. Lane P: free probe without protein extract. Panel B: EMSA was performed on pathologic cytoplasmic extracts from colorectal cancer (K1-K6) and adenoma (A1-A9) patients. Lane P: free probe without protein extract.
- Citation: Mazzarelli P, Parrella P, Seripa D, Signori E, Perrone G, Rabitti C, Borzomati D, Gabbrielli A, Matera MG, Gravina C, Caricato M, Poeta ML, Rinaldi M, Valeri S, Coppola R, Fazio VM. DNA end binding activity and Ku70/80 heterodimer expression in human colorectal tumor. World J Gastroenterol 2005; 11(42): 6694-6700
- URL: https://www.wjgnet.com/1007-9327/full/v11/i42/6694.htm
- DOI: https://dx.doi.org/10.3748/wjg.v11.i42.6694