Literature DB >> 21400290

Single Specific Primer-Polymerase Chain Reaction (SSP-PCR) and Genome Walking.

V Shyamala1, G Ferro-Luzzi Ames.   

Abstract

The polymerase chain reaction (PCR) is used for selective amplification of DNA fragments from both prokaryotes and eukaryotes (1-3). The only requirement for amplification is that the sequence of the extremities of the DNA fragment to be amplified be known (4). This places a limitation on the use of PCR in the amplification of adjacent unknown regions. We have developed a method that allows the amplification of double-stranded DNA even when the sequence information is available at one end only (5). This method, the single specific primer-PCR (SSP-PCR), permits amplification of genes for which only a partial sequence information is available, and allows unidirectional genome walking from known into unknown regions of the chromosome.

Year:  1993        PMID: 21400290     DOI: 10.1385/0-89603-244-2:339

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  3 in total

1.  Clostridium sordellii phospholipase C: gene cloning and comparison of enzymatic and biological activities with those of Clostridium perfringens and Clostridium bifermentans phospholipase C.

Authors:  Tadahiro Karasawa; Xingmin Wang; Tsuneo Maegawa; Yoshio Michiwa; Hiroyuki Kita; Koichi Miwa; Shinichi Nakamura
Journal:  Infect Immun       Date:  2003-02       Impact factor: 3.441

2.  B12-dependent ribonucleotide reductases from deeply rooted eubacteria are structurally related to the aerobic enzyme from Escherichia coli.

Authors:  A Jordan; E Torrents; C Jeanthon; R Eliasson; U Hellman; C Wernstedt; J Barbé; I Gibert; P Reichard
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-09       Impact factor: 11.205

3.  Optimization of an in-house PCR method for the detection of HLA-B*27 alleles.

Authors:  Noor Afshan; Mukarram Bashir; Hamid Nawaz Tipu; Mohammad Hussain
Journal:  Biomed Rep       Date:  2018-02-01
  3 in total

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