Fomin V V, Borisov M B, Zaĭtsev A V, Blokhin D Iu
Biull Eksp Biol Med. 1993 Apr;115(4):416-8.
Methods, used for indirect determination of single-thread breaks' quantity in DNA, based on it's denaturation in alkali medium and further determination of double-thread DNA quantity by it's fluorescence has been adapted to the measuring of thread disturbances on leukemia P-388 cells. Influence of cells' and alkali concentrations and the time of denaturation of quantity of double-thread DNA has been investigated.
基于DNA在碱性介质中的变性以及通过荧光进一步测定双链DNA数量来间接测定DNA中单链断裂数量的方法,已适用于测量白血病P - 388细胞中的链干扰情况。研究了细胞浓度、碱浓度以及双链DNA数量变性时间的影响。