Home LiteratureArticle Details

PMID: 1549491 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Pre-boiling high GC content, mixed primers with 3' complementation allows the successful PCR amplification of Pseudomonas aeruginosa DNA.

Nucleic acids research ·Vol. 20 ·No. 5 ·1992-03-11 ·Pages 1155

Kureishi A, Bryan LE

Abstract

暂无摘要

Related Genes

gyrA

MeSH Terms

Base Composition/genetics Base Sequence DNA, Bacterial/genetics Molecular Sequence Data Oligodeoxyribonucleotides/genetics Polymerase Chain Reaction/methods Pseudomonas aeruginosa/genetics Temperature

Chemicals

DNA, Bacterial Oligodeoxyribonucleotides

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Kureishi A

Department of Microbiology & Infectious Diseases, University of Calgary, Alberta, Canada.

Bryan L E

References (3)

3 references, click to expand

DNA cloning and organization of the Staphylococcus aureus gyrA and gyrB genes: close homology among gyrase proteins and implications for 4-quinolone action and resistance.
J Bacteriol. 1990 Jun;172(6):3481-4 PMID: 2160946
Base pairing involving deoxyinosine: implications for probe design.
Nucleic Acids Res. 1985 Dec 20;13(24):8927-38 PMID: 4080553
Cloning and sequencing of the Escherichia coli gyrA gene coding for the A subunit of DNA gyrase.
J Mol Biol. 1987 Oct 20;197(4):729-36 PMID: 2828631

Article Info

Journal

Nucleic acids research

Abbr.

Nucleic Acids Res

ISSN

0305-1048

DOI

10.1093/nar/20.5.1155

Published

1992-03-11

Pages

1155

Language

English

Region

England

NLM ID

0411011

PMCID

PMC312118

Subset

External Links

PubMed source DOI: 10.1093/nar/20.5.1155 PMC Full Text View journal details

Analysis Services

Pre-boiling high GC content, mixed primers with 3' complementation allows the successful PCR amplification of Pseudomonas aeruginosa DNA.

Contact

WeChat Official Account