Roeder T
University of Hamburg, Zoological Institute, Department of Neurophysiology, Martin-Luther-King-Platz 3,D-20146 Hamburg, Germany.
Nucleic Acids Res. 1998 Jul 15;26(14):3451-2. doi: 10.1093/nar/26.14.3451.
A rapid and versatile method for cDNA library construction was developed. It is based on conventional cDNA library synthesis including all enzymatic steps usually required, but is performed on a solid support. The cDNA is immobilised via a biotin residue to streptavidin coupled magnetic beads, which allows rapid and easy to perform changes of buffers and enzymes. Therefore, it combines speed (library construction within a single day) with high quality libraries, making it ideally suited for most purposes.
开发了一种快速且通用的cDNA文库构建方法。它基于常规的cDNA文库合成,包括通常所需的所有酶促步骤,但在固体支持物上进行。cDNA通过生物素残基固定在与链霉亲和素偶联的磁珠上,这使得缓冲液和酶的更换快速且易于操作。因此,它将速度(一天内构建文库)与高质量文库相结合,使其非常适合大多数用途。