Inverse Polymerase Chain Reaction
- Sheng-He HuangAffiliated withDivision of Infectious Disease Department of Pediatrics, University of Southern California Children’ Hospital of Los Angeles
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Since the first report on cDNA cloning in 1972 (1), this technology has been developed into a powerful and universal tool in the isolation, characterization, and analysis of both eukaryotic and prokaryotic genes. But the conventional methods of cDNA cloning require much effort to generate a library that is packaged in phage or plasmid and then survey a large number of recombinant phages or plasmids. There are three major limitations in those methods. First, substantial amount (at least 1 µg) of purified mRNA is needed as starting material to generate libraries of sufficient diversity (2). Second, the intrinsic difficulty of multiple sequential enzymatic reactions required for cDNA cloning often leads to low yields and truncated clones (3). Finally, screening of a library with hybridization technique is time consuming.
- Inverse Polymerase Chain Reaction
- Book Title
- The Nucleic Acid Protocols Handbook
- Book Part
- pp 625-631
- Print ISBN
- Online ISBN
- Humana Press
- Copyright Holder
- Humana Press Inc., Totowa, NJ
- Additional Links
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