1991
DOI: 10.1016/0003-2697(91)90092-8
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Direct sequencing of double-stranded polymerase chain reaction-amplified 16S rDNA

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Cited by 24 publications
(15 citation statements)
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“…The 16S rRNA gene was amplified according to Both et al . The set of primers used in this experiment were 5′‐AGAGTTTGATCCTGGCTCAGAACGAACGCT‐3′ (positions 8–37) and 5′‐TACGGCTACCTTGTTACGACTTCACCCC‐3′ (positions 1479–1506) according to the Escherichia coli numbering system.…”
Section: Methodsmentioning
confidence: 99%
“…The 16S rRNA gene was amplified according to Both et al . The set of primers used in this experiment were 5′‐AGAGTTTGATCCTGGCTCAGAACGAACGCT‐3′ (positions 8–37) and 5′‐TACGGCTACCTTGTTACGACTTCACCCC‐3′ (positions 1479–1506) according to the Escherichia coli numbering system.…”
Section: Methodsmentioning
confidence: 99%
“…intergenic spacer region PCR was performed as described by Both et al [13]. Primers used for amplification of the spacer region were Al 6 : 5'-TTGCATGGATCCTGCGG-CTGGATCACCTCC-3' and B23 : 5'-GAATCAG-GATCCGAATGCCCTTATCGCGCTC-3'.…”
Section: In Vitro Ampkjication and Cloning Of The 16s-23smentioning
confidence: 99%
“…16S ribosomal DNA (rDNA) was amplified in vitro (PCR) by using the method of Both et al (1) in combination with oligonucleotide primers complementary to highly conserved regions of bacterial rRNA genes. The 5Ј-and 3Ј-terminal primers used were GAGTTTGAT(C/T)(C/A)TGGCTCA (positions 9 to 26, according to the E. coli numbering system [2]) and CA(G/T)AAAGGAGGTGATCC (positions 1545 to 1529), respectively (11).…”
mentioning
confidence: 99%