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In vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory.
The acceptance of nucleic acid probes as diagnostic tools for the clinical laboratory has been hampered by a number of factors, including laborious techniques and limited sensitivity. The focus of this review is on the recent development of amplification techniques to enhance the signal generated by...
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Formato: | Texto |
Lenguaje: | English |
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Yale Journal of Biology and Medicine
1989
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2589213/ https://www.ncbi.nlm.nih.gov/pubmed/2672619 |
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author | Persing, D. H. Landry, M. L. |
author_facet | Persing, D. H. Landry, M. L. |
author_sort | Persing, D. H. |
collection | PubMed |
description | The acceptance of nucleic acid probes as diagnostic tools for the clinical laboratory has been hampered by a number of factors, including laborious techniques and limited sensitivity. The focus of this review is on the recent development of amplification techniques to enhance the signal generated by nucleic acid-based detection systems. Three general areas are discussed: (1) amplification of target sequences using the polymerase chain reaction or the transcript amplification system, (2) amplification of the probe sequences using Q beta replicase, and (3) amplification of probe-generated signals with compound or "Christmas tree" probes. The hope of these new technologies is to simplify yet improve on the sensitivity of nucleic acid-based tests to enable them to attain a more prominent place in the diagnostic repertoire of the clinical laboratory. |
format | Text |
id | pubmed-2589213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | Yale Journal of Biology and Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-25892132008-11-28 In vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory. Persing, D. H. Landry, M. L. Yale J Biol Med Research Article The acceptance of nucleic acid probes as diagnostic tools for the clinical laboratory has been hampered by a number of factors, including laborious techniques and limited sensitivity. The focus of this review is on the recent development of amplification techniques to enhance the signal generated by nucleic acid-based detection systems. Three general areas are discussed: (1) amplification of target sequences using the polymerase chain reaction or the transcript amplification system, (2) amplification of the probe sequences using Q beta replicase, and (3) amplification of probe-generated signals with compound or "Christmas tree" probes. The hope of these new technologies is to simplify yet improve on the sensitivity of nucleic acid-based tests to enable them to attain a more prominent place in the diagnostic repertoire of the clinical laboratory. Yale Journal of Biology and Medicine 1989 /pmc/articles/PMC2589213/ /pubmed/2672619 Text en |
spellingShingle | Research Article Persing, D. H. Landry, M. L. In vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory. |
title | In vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory. |
title_full | In vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory. |
title_fullStr | In vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory. |
title_full_unstemmed | In vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory. |
title_short | In vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory. |
title_sort | in vitro amplification techniques for the detection of nucleic acids: new tools for the diagnostic laboratory. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2589213/ https://www.ncbi.nlm.nih.gov/pubmed/2672619 |
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