EJBiotechnology logo
Electronic Journal of Biotechnology ISSN: 0717-3458
  © 2010 by Universidad Católica de Valparaíso -- Chile
Vol. 13 No. 5, Issue of September 15, 2010
 


Figure 4. Agarose gel electrophoresis of chromosomal DNA of 3 x 106 cells of (A) variouscancer cells and (B) normal cells treated with the extracts at 37ºC for 24 hrs in 5%CO2.
(A) M = molecular weight marker; P = Positive control; lane 1, U937 cells untreated; lane 2, U937 treated with Ys102 extract; lane 3, HeLa untreated; lane 4, HeLa with B92 extract; lane 5, HepG2 untreated; lane 6, HepG2 cells with B151 extract; lane 7, MCF-7 untreated; and lane 8, MCF-7 treated with B100 extract.
(B) M = molecular weight marker; lane 1, PBMC treated with Ys102 extract; lane 2, Vero cells treated with Ys102 extract; lane 3, PBMC treated with B92 extract; lane 4, Vero cell treated with B92 extract; lane 5, PBMC treated with B151 extract; lane 6, Vero cell treated with B151 extract; lane 7, PBMC treated with B100 extract; lane 8, Vero cell treated with B100 extract.


Supported by UNESCO / MIRCEN network