Comparison of real-time PCR with SYBR Green I or 5'-nuclease assays and dot-blot hybridization with rDNA-targeted oligonucleotide probes in quantification of selected faecal bacteria
Clicks: 398
ID: 110520
2003
Article Quality & Performance Metrics
Overall Quality
Improving Quality
0.0
/100
Combines engagement data with AI-assessed academic quality
Reader Engagement
Emerging Content
0.3
/100
1 views
1 readers
Trending
AI Quality Assessment
Not analyzed
Abstract
PCR primers and hybridization probes were designed for the 16S rRNA genes of six bacterial species or groups typically present in human faeces or used in the dairy industry. The primers and probes were applied for quantification of the target bacterial genomes added in artificial DNA mixtures or fae …Reference Key |
e2003microbiologycomparison
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
---|---|
Authors | Malinen E;Kassinen A;Rinttilä T;Palva A;; |
Journal | Microbiology (Reading, England) |
Year | 2003 |
DOI | DOI not found |
URL | |
Keywords |
National Center for Biotechnology Information
NCBI
NLM
MEDLINE
RNA
humans
pubmed abstract
nih
national institutes of health
national library of medicine
research support
non-u.s. gov't
Comparative Study
DNA
Ribosomal
16S / genetics
pmid:12576600
doi:10.1099/mic.0.25975-0
Evaluation Study
Erja Malinen
Anna Kassinen
Airi Palva
Bacteria / genetics
Bacteria / isolation & purification*
Bacterial / analysis
Ribosomal / analysis
Feces / microbiology*
Fluorescent Dyes / metabolism
Immunoblotting
Nucleic Acid Hybridization / methods*
Oligonucleotide Probes*
Organic Chemicals*
Polymerase Chain Reaction / methods*
Taq Polymerase / metabolism
|
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.