Frumgarts L A, Kipriianov S M, Kalachikov S M, Dudareva N A, Dymshits G M
Bioorg Khim. 1986 Nov;12(11):1508-13.
A method of the fluorescent-labeled DNA preparation for visualization of the complementary nucleotide sequences has been developed. Polynucleotide probes were alkylated randomly by 4-(N-methylamino-N-2-chloroethyl)-benzylamine followed by modification with such fluorochromes as dansyl chloride or fluorescein isothiocyanate (FITC). It was found that the FITC but not dansyl-labeled polynucleotides could serve as efficient probes when about 4% of nitrogen bases were modified. The conditions minimizing the loss of the alkylated bases from DNA were determined. The procedure for hybridization with FITC-labeled DNA as a probe is described, concentration of DNA probe being about 4 ng/mm2 of the nitrocellulose filter.
已开发出一种用于可视化互补核苷酸序列的荧光标记DNA制备方法。多核苷酸探针先用4-(N-甲基氨基-N-2-氯乙基)苄胺进行随机烷基化,然后用丹磺酰氯或异硫氰酸荧光素(FITC)等荧光染料进行修饰。结果发现,当约4%的氮碱基被修饰时,FITC标记的多核苷酸而非丹磺酰标记的多核苷酸可作为有效的探针。确定了使DNA中烷基化碱基损失最小的条件。描述了以FITC标记的DNA为探针的杂交程序,DNA探针的浓度约为硝酸纤维素滤膜4 ng/mm²。