The inclusivity, exclusivity, and detection limit of six 16S rRNA gene-based Helicobacter genus-specific PCR assays were examined. Five out of six assays were 100% inclusive, but the tests varied considerably in their exclusivity (9.1 to 95.5%). The clinical detection limit varied between 10(3) and 1 viable bacterial cell per reaction mixture
Molecular detection and classification of the bacterial groups in a sample are relevant in several a...
<p>(lanes M: step-ladder marker; 1: positive control of gastric biopsy-derived <i>H. pylori</i> DNA;...
A 1.9-kb cloned fragment of chromosomal DNA randomly selected from a Helicobacterpylori cloned libra...
The inclusivity, exclusivity, and detection limit of six 16S rRNA gene-based Helicobacter genus-spec...
AbstractThe present study aimed to establish a genus-specific PCR-based assay to detect helicobacter...
Sequence data on Helicobacter pylori 16S rRNA were used to select two 22-base oligonucleotide primer...
Using polymerase chain reaction (PCR), we examined 16S ribosomal DNA (rDNA) of Helicobacter species ...
Within the paradigm of clinical infectious disease research, Acinetobacter baumannii, Escherichia co...
Helicobacter infections of laboratory animals may influence the results of in vivo experiments, nece...
Helicobacter species are fastidious bacterial pathogens that are difficult to culture by standard me...
Amplification and sequence analysis of the 16S rRNA gene can be applied to detect and identify bacte...
<div><p>Within the paradigm of clinical infectious disease research, <em>Acinetobacter baumannii</em...
We report the design and evaluation of PCR primers 63f and 1387r for amplification of 16S rRNA genes...
Here we determined the analytical sensitivities of broad-range real-time PCR-based assays employing ...
Broad-range real-time PCR and sequencing of the 16S rRNA gene region is a widely known method for th...
Molecular detection and classification of the bacterial groups in a sample are relevant in several a...
<p>(lanes M: step-ladder marker; 1: positive control of gastric biopsy-derived <i>H. pylori</i> DNA;...
A 1.9-kb cloned fragment of chromosomal DNA randomly selected from a Helicobacterpylori cloned libra...
The inclusivity, exclusivity, and detection limit of six 16S rRNA gene-based Helicobacter genus-spec...
AbstractThe present study aimed to establish a genus-specific PCR-based assay to detect helicobacter...
Sequence data on Helicobacter pylori 16S rRNA were used to select two 22-base oligonucleotide primer...
Using polymerase chain reaction (PCR), we examined 16S ribosomal DNA (rDNA) of Helicobacter species ...
Within the paradigm of clinical infectious disease research, Acinetobacter baumannii, Escherichia co...
Helicobacter infections of laboratory animals may influence the results of in vivo experiments, nece...
Helicobacter species are fastidious bacterial pathogens that are difficult to culture by standard me...
Amplification and sequence analysis of the 16S rRNA gene can be applied to detect and identify bacte...
<div><p>Within the paradigm of clinical infectious disease research, <em>Acinetobacter baumannii</em...
We report the design and evaluation of PCR primers 63f and 1387r for amplification of 16S rRNA genes...
Here we determined the analytical sensitivities of broad-range real-time PCR-based assays employing ...
Broad-range real-time PCR and sequencing of the 16S rRNA gene region is a widely known method for th...
Molecular detection and classification of the bacterial groups in a sample are relevant in several a...
<p>(lanes M: step-ladder marker; 1: positive control of gastric biopsy-derived <i>H. pylori</i> DNA;...
A 1.9-kb cloned fragment of chromosomal DNA randomly selected from a Helicobacterpylori cloned libra...