Polymerase chain reaction |
| |
Authors: | Henry A. Erlich |
| |
Affiliation: | (1) Department of Human Genetics, Cetus Corporation, 1400 53rd Street, 94608 Emeryville, California |
| |
Abstract: | Summary The PCR, like recombinant DNA technology, has had an enormous impact in both basic and diagnostic aspects of molecular biology because it can produce large amounts of a specific DNA fragment from small amounts of a complex template. Recombinant DNA techniques create molecular clones by conferring on a specific sequence the ability to replicate by inserting it into a vector and introducing the vector into a host cell. PCR represents a form of in vitro cloning that can generate, as well as modify, DNA fragments of defined length and sequence in a simple automated reaction. In addition to its many applications in basic molecular biological research, PCR promises to play a critical role in the identification of medically important sequences as well as an important diagnostic one in their detection. |
| |
Keywords: | Polymerase chain reaction DNA denaturing gradient gel electrophoresis |
本文献已被 SpringerLink 等数据库收录! |
|