Martin C S
Tropix, Inc., Bedford, Massachusetts, USA.
Curr Protoc Mol Biol. 2001 May;Chapter 7:Unit7.4B. doi: 10.1002/0471142727.mb0704bs47.
Standard dideoxy DNA sequencing can be performed easily and efficiently with nonisotopic, chemiluminescent detection by utilizing primers labeled with biotin in the sequencing reactions. As described in this unit, reaction products are separated by denaturing gel electrophoresis, transferred to a nylon membrane, and detected by first binding a streptavidin-alkaline phosphatase conjugate, then incubating with a chemiluminescent 1,2-dioxetane substrate. The emitted light signal is imaged on standard X-ray film, producing high-resolution DNA sequencing ladders. Indirect alkaline phosphatase-labeling of biotinylated DNA with free streptavidin and biotinylated alkaline phosphatase is also detailed, Finally, the detection of sequencing reactions labeled with other haptens using specific antibody-alkaline phosphatase conjugates is described.
通过在测序反应中使用生物素标记的引物,标准双脱氧DNA测序可以轻松、高效地采用非同位素化学发光检测法进行。如本单元所述,反应产物通过变性凝胶电泳分离,转移至尼龙膜上,首先结合链霉亲和素-碱性磷酸酶偶联物,然后与化学发光的1,2-二氧杂环丁烷底物孵育进行检测。发射的光信号在标准X光片上成像,产生高分辨率的DNA测序梯。还详细介绍了用游离链霉亲和素和生物素化碱性磷酸酶对生物素化DNA进行间接碱性磷酸酶标记。最后,描述了使用特异性抗体-碱性磷酸酶偶联物检测用其他半抗原标记的测序反应。