(PDF) PCR Amplification and Direct Sequencing of gyrB Genes

PCR Amplification and Direct Sequencing of gyrB Genes With Universal Primers and Their Application to the Detection and Taxonomic Analysis of Pseudomonas Putida Strains.

Applied and Environmental Microbiology - United States

doi 10.1128/aem.61.3.1104-1109.1995

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Abstract

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Date

January 1, 1995

Authors

S Yamamoto

S Harayama

Publisher

American Society for Microbiology

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PCR Amplification and Direct Sequencing of gyrB Genes With Universal Primers and Their Application to the Detection and Taxonomic Analysis of Pseudomonas Putida Strains.

Applied and Environmental Microbiology - United States

doi 10.1128/aem.61.3.1104-1109.1995

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

PCR Amplification and Direct Sequencing of gyrB Genes With Universal Primers and Their Application to the Detection and Taxonomic Analysis of Pseudomonas Putida Strains.

Application of Qualitative and Quantitative Real-Time PCR, Direct Sequencing, and Terminal Restriction Fragment Length Polymorphism Analysis for Detection and Identification of Polymicrobial 16S rRNA Genes in Ascites

Table S2: Primers Used in PCR and Sequencing

Molecular Diagnosis of Helicobacter Pylori Strain by 16S rDNA PCR Amplification and Direct Sequencing

Phylogenetic Analysis of Acinetobacter Strains Based on the Nucleotide Sequences of gyrB Genes and on the Amino Acid Sequences of Their Products

PCR Amplification and Sequencing Analysis of Full-Length Turkey Coronavirus Spike Gene

Table 1: PCR Primers and Conditions for the Amplification of the Tested Markers.

PCR Amplification on a Microarray of Gel-Immobilized Oligonucleotides: Detection of Bacterial Toxin- And Drug-Resistant Genes and Their Mutations

Use of PCR With Universal Primers and Restriction Endonuclease Digestions for Detection and Identification of Common Bacterial Pathogens in Cerebrospinal Fluid