Selective amplification of cDNA sequence from total RNA by cassette-ligation mediated polymerase chain reaction (PCR): Application to sequencing 6·5 kb genome segment of hantavirus strain B-1-Reference-Cited by-同舟云学术

Selective amplification of cDNA sequence from total RNA by cassette-ligation mediated polymerase chain reaction (PCR): Application to sequencing 6·5 kb genome segment of hantavirus strain B-1

Published:1992-12 Issue:6 Volume:6 Page:467-475
ISSN:0890-8508
Container-title:Molecular and Cellular Probes
language:en
Short-container-title:Molecular and Cellular Probes

Author:

Isegawa Yuji,Sheng Jun,Sokawa Yoshihiro,Yamanishi Koichi,Nakagomi Osamu,Ueda Shigeharu

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference18 articles.

1. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase;Saiki;Science,1988

2. Genetic applications of an inverse polymerase chain reaction;Ochman;Genetics,1988

3. A procedure for in vitro amplification of DNA segments that lie outside the boundaries on known sequences;Triglia;Nucleic Acids Research,1988

4. A simple method for direct cloning cDNA sequence that flanks a region of known sequence from total RNA by applying the inverse polymerase chain reaction;Huang;Nucleic Acids Research,1990

5. Genomic walking and sequencing by oligo-cassette mediated polymerase chain reaction;Rosenthal;Nucleic Acids Research,1990

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