The 15 mL DNA and 3 mL 6 DNA loadi

The 15 mL DNA and 3 mL 6 DNA loading buffer mixed samples
were added intowells of 1% agarose gel in TAE containing 0.5 mg/mL
ethidium bromide. Gel electrophoresis was run at 60 V for 2 h. DNA
ladders were finally visualized by a UV light source and documented
by photography. DNA extracted from apoptotic cells
showed a distinct DNA ladder, and DNA from viable cells stayed on
the top of the gel as a high-molecular weight band.

結果 (中文) 1:

15 毫升 DNA 和 3 毫升 6 DNA 加载缓冲混合样品在含有 0.5 毫克/毫升的泰中添加 1%琼脂糖凝胶 intowells溴化乙锭。运行为 60 V，2 h.DNA 凝胶电泳梯子最后由紫外光源可视化及记录由摄影。从凋亡细胞中提取 DNA显示不同的 DNA 梯，并留任的可行细胞 DNA 从作为一个高分子量乐队凝胶的顶部。

結果 (中文) 3:

15毫升和3毫升6  DNA DNA上样缓冲液混合样品进行
TAE中含有0.5毫克/毫升
溴化乙锭加入1%琼脂糖凝胶intowells。凝胶电泳运行在60伏的2小时。dna的梯子，最后通过一个紫外线光源和记录的摄影，通过摄影。从凋亡细胞中提取dna，显示出不同的dna，并在存活的细胞中存活作为一个高的分子量带的凝胶的顶部。