Potential risks of gene amplification by PCR as determined by 16S rDNA analysis of a mixed-culture of strict barophilic bacteria (Q58425247)

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29 February 2020

title

Potential risks of gene amplification by PCR as determined by 16S rDNA analysis of a mixed-culture of strict barophilic bacteria (English)

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29 February 2020

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1

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29 February 2020

Erko Stackebrandt

series ordinal

3

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29 February 2020

author name string

H Weyland

series ordinal

2

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publication date

1 December 1991

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29 February 2020

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volume

21

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issue

1

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29 February 2020

page(s)

191-198

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https://scigraph.springernature.com/pub.10.1007/bf02539153

29 February 2020

exact match

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cites work

Rapid Generation of Vector-Free Digoxygenin-dUTP Labeled Probes for Nonradioactive Hybridization Using the Polymerase Chain Reaction (PCR) Method

1 reference

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Nucleotide Sequence of the 16S rRNA from Vibrio anguillarum

21 January 2018

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A non-sequential method for constructing trees and hierarchical classifications

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Genetic diversity in Sargasso Sea bacterioplankton

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Conservation of the primary structure at the 3' end of 18S rRNA from eucaryotic cells

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12 December 2020

16S rRNA sequences reveal numerous uncultured microorganisms in a natural community

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12 December 2020

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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12 December 2020

Production of single-stranded DNA templates by exonuclease digestion following the polymerase chain reaction.

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12 December 2020

Development and application of oligonucleotide probes for molecular identification of Xenorhabdus species.

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12 December 2020

Selective Recovery of 16S rRNA Sequences from Natural Microbial Communities in the Form of cDNA

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12 December 2020

Optimal conditions for directly sequencing double-stranded PCR products with sequenase

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12 December 2020

Recovery of DNA from soils and sediments

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Compilation of small ribosomal subunit RNA sequences

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12 December 2020

Identifiers

DOI

10.1007/BF02539153

1 reference

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29 February 2020

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