Modified linker-PCR primers facilitate complete sequencing of DGGE DNA fragments

Journal of Microbiological Methods

Volumn 75, Issue 3, 2008, Pages 579-581

  O'Sullivan, Louise A ^a   Webster, Gordon ^a   Fry, John C ^a   Parkes, R John ^b   Weightman, Andrew J ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

^b CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

16S rRNA genes; Archaea; Bacteria; PCR DGGE; Prokaryotic diversity

Indexed keywords

BACTERIAL RNA; DNA FRAGMENT; PRIMER DNA; RIBOSOME RNA;

ARCHAEBACTERIUM; ARTICLE; BACTERIAL GENE; CONTROLLED STUDY; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA MODIFICATION; DNA SEQUENCE; HALOBACTERIUM SALINARUM; METHANOBACTERIUM BRYANTII; METHANOSARCINA BARKERI; METHANOSPIRILLUM HUNGATEI; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ARCHAEA; BACTERIA; DNA PRIMERS; DNA, ARCHAEAL; DNA, BACTERIAL; DNA, RIBOSOMAL; ELECTROPHORESIS, POLYACRYLAMIDE GEL; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; RNA, RIBOSOMAL, 16S; SEQUENCE ANALYSIS, DNA;

ARCHAEA; BACTERIA (MICROORGANISMS); PROKARYOTA;

EID: 55149123344     PISSN: 01677012     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mimet.2008.08.006     Document Type: Article

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