Loading…

Quantitative PCR : a survey of the present technology

PCR-based amplification of nucleic acids has had a major impact in almost every field of basic research and has already found extensive applications in the area of clinical diagnosis. For many of these applications, quantitative data are sought to relate the quantity of amplified product to the amou...

Full description

Saved in:
Bibliographic Details
Published in:Molecular biotechnology 1995-02, Vol.3 (1), p.55-71
Main Authors: REISCHL, U, KOCHANOWSKI, B
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c306t-a2d4578d5d6ccdb83c2fc33244263aaf8e929586c0a7b41eab2624e95f10bd593
container_end_page 71
container_issue 1
container_start_page 55
container_title Molecular biotechnology
container_volume 3
creator REISCHL, U
KOCHANOWSKI, B
description PCR-based amplification of nucleic acids has had a major impact in almost every field of basic research and has already found extensive applications in the area of clinical diagnosis. For many of these applications, quantitative data are sought to relate the quantity of amplified product to the amount of original target nucleic acid present in the sample. Since the PCR methodology with its exponential nature can be adapted for this purpose, a lot of different strategies have emerged in the last few years for sensitive and specific PCR product detection and quantification. Basic strategies, including the use of external and internal standards, are presented with respect to statistical aspects, and the advantages as well as the limitations of individual protocols are discussed. Furthermore the suitability of conventional laboratory techniques, such as gel systems or HPLC, nonradioactive labeling procedures, and the principles of advanced solid-phase-mediated strategies for the precise determination of amplification products, are outlined with the help of selected examples.
doi_str_mv 10.1007/BF02821335
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_77380388</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77380388</sourcerecordid><originalsourceid>FETCH-LOGICAL-c306t-a2d4578d5d6ccdb83c2fc33244263aaf8e929586c0a7b41eab2624e95f10bd593</originalsourceid><addsrcrecordid>eNpFkEtLw0AUhQdRaq1u3AuzEBdC9M7czCPutPiCgg90HSaTiY2kSZ2ZFPrvjbTU1TlwPs7iI-SUwRUDUNd3D8A1Z4hij4yZEFkCCGJ_6KAwkaDFITkK4RuAM5HiiIyUBClAjIl4600b62hivXL0dfpOb6ihofcrt6ZdRePc0aV3wbWRRmfnbdd0X-tjclCZJriTbU7I58P9x_Qpmb08Pk9vZ4lFkDExvEyF0qUopbVlodHyyiLyNOUSjam0y3gmtLRgVJEyZwoueeoyUTEoSpHhhFxsfpe---ldiPmiDtY1jWld14dcKdSAWg_g5Qa0vgvBuypf-nph_DpnkP85yv8dDfDZ9rUvFq7coVspw36-3U2wpqm8aW0ddhgKgagV_gLj8mvr</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>77380388</pqid></control><display><type>article</type><title>Quantitative PCR : a survey of the present technology</title><source>SpringerLink_过刊(NSTL购买)</source><creator>REISCHL, U ; KOCHANOWSKI, B</creator><creatorcontrib>REISCHL, U ; KOCHANOWSKI, B</creatorcontrib><description>PCR-based amplification of nucleic acids has had a major impact in almost every field of basic research and has already found extensive applications in the area of clinical diagnosis. For many of these applications, quantitative data are sought to relate the quantity of amplified product to the amount of original target nucleic acid present in the sample. Since the PCR methodology with its exponential nature can be adapted for this purpose, a lot of different strategies have emerged in the last few years for sensitive and specific PCR product detection and quantification. Basic strategies, including the use of external and internal standards, are presented with respect to statistical aspects, and the advantages as well as the limitations of individual protocols are discussed. Furthermore the suitability of conventional laboratory techniques, such as gel systems or HPLC, nonradioactive labeling procedures, and the principles of advanced solid-phase-mediated strategies for the precise determination of amplification products, are outlined with the help of selected examples.</description><identifier>ISSN: 1073-6085</identifier><identifier>EISSN: 1559-0305</identifier><identifier>DOI: 10.1007/BF02821335</identifier><identifier>PMID: 7606505</identifier><identifier>CODEN: MLBOEO</identifier><language>eng</language><publisher>Totowa, NJ: Humana Press</publisher><subject>Biological and medical sciences ; Biotechnology ; Fundamental and applied biological sciences. Psychology ; Genetic engineering ; Genetic technics ; In vitro gene amplification. Pcr technique ; Methods. Procedures. Technologies ; Polymerase Chain Reaction - methods ; Polymerase Chain Reaction - standards</subject><ispartof>Molecular biotechnology, 1995-02, Vol.3 (1), p.55-71</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c306t-a2d4578d5d6ccdb83c2fc33244263aaf8e929586c0a7b41eab2624e95f10bd593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3553387$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7606505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>REISCHL, U</creatorcontrib><creatorcontrib>KOCHANOWSKI, B</creatorcontrib><title>Quantitative PCR : a survey of the present technology</title><title>Molecular biotechnology</title><addtitle>Mol Biotechnol</addtitle><description>PCR-based amplification of nucleic acids has had a major impact in almost every field of basic research and has already found extensive applications in the area of clinical diagnosis. For many of these applications, quantitative data are sought to relate the quantity of amplified product to the amount of original target nucleic acid present in the sample. Since the PCR methodology with its exponential nature can be adapted for this purpose, a lot of different strategies have emerged in the last few years for sensitive and specific PCR product detection and quantification. Basic strategies, including the use of external and internal standards, are presented with respect to statistical aspects, and the advantages as well as the limitations of individual protocols are discussed. Furthermore the suitability of conventional laboratory techniques, such as gel systems or HPLC, nonradioactive labeling procedures, and the principles of advanced solid-phase-mediated strategies for the precise determination of amplification products, are outlined with the help of selected examples.</description><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>In vitro gene amplification. Pcr technique</subject><subject>Methods. Procedures. Technologies</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Polymerase Chain Reaction - standards</subject><issn>1073-6085</issn><issn>1559-0305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNpFkEtLw0AUhQdRaq1u3AuzEBdC9M7czCPutPiCgg90HSaTiY2kSZ2ZFPrvjbTU1TlwPs7iI-SUwRUDUNd3D8A1Z4hij4yZEFkCCGJ_6KAwkaDFITkK4RuAM5HiiIyUBClAjIl4600b62hivXL0dfpOb6ihofcrt6ZdRePc0aV3wbWRRmfnbdd0X-tjclCZJriTbU7I58P9x_Qpmb08Pk9vZ4lFkDExvEyF0qUopbVlodHyyiLyNOUSjam0y3gmtLRgVJEyZwoueeoyUTEoSpHhhFxsfpe---ldiPmiDtY1jWld14dcKdSAWg_g5Qa0vgvBuypf-nph_DpnkP85yv8dDfDZ9rUvFq7coVspw36-3U2wpqm8aW0ddhgKgagV_gLj8mvr</recordid><startdate>19950201</startdate><enddate>19950201</enddate><creator>REISCHL, U</creator><creator>KOCHANOWSKI, B</creator><general>Humana Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19950201</creationdate><title>Quantitative PCR : a survey of the present technology</title><author>REISCHL, U ; KOCHANOWSKI, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-a2d4578d5d6ccdb83c2fc33244263aaf8e929586c0a7b41eab2624e95f10bd593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>In vitro gene amplification. Pcr technique</topic><topic>Methods. Procedures. Technologies</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Polymerase Chain Reaction - standards</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>REISCHL, U</creatorcontrib><creatorcontrib>KOCHANOWSKI, B</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>REISCHL, U</au><au>KOCHANOWSKI, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative PCR : a survey of the present technology</atitle><jtitle>Molecular biotechnology</jtitle><addtitle>Mol Biotechnol</addtitle><date>1995-02-01</date><risdate>1995</risdate><volume>3</volume><issue>1</issue><spage>55</spage><epage>71</epage><pages>55-71</pages><issn>1073-6085</issn><eissn>1559-0305</eissn><coden>MLBOEO</coden><abstract>PCR-based amplification of nucleic acids has had a major impact in almost every field of basic research and has already found extensive applications in the area of clinical diagnosis. For many of these applications, quantitative data are sought to relate the quantity of amplified product to the amount of original target nucleic acid present in the sample. Since the PCR methodology with its exponential nature can be adapted for this purpose, a lot of different strategies have emerged in the last few years for sensitive and specific PCR product detection and quantification. Basic strategies, including the use of external and internal standards, are presented with respect to statistical aspects, and the advantages as well as the limitations of individual protocols are discussed. Furthermore the suitability of conventional laboratory techniques, such as gel systems or HPLC, nonradioactive labeling procedures, and the principles of advanced solid-phase-mediated strategies for the precise determination of amplification products, are outlined with the help of selected examples.</abstract><cop>Totowa, NJ</cop><pub>Humana Press</pub><pmid>7606505</pmid><doi>10.1007/BF02821335</doi><tpages>17</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1073-6085
ispartof Molecular biotechnology, 1995-02, Vol.3 (1), p.55-71
issn 1073-6085
1559-0305
language eng
recordid cdi_proquest_miscellaneous_77380388
source SpringerLink_过刊(NSTL购买)
subjects Biological and medical sciences
Biotechnology
Fundamental and applied biological sciences. Psychology
Genetic engineering
Genetic technics
In vitro gene amplification. Pcr technique
Methods. Procedures. Technologies
Polymerase Chain Reaction - methods
Polymerase Chain Reaction - standards
title Quantitative PCR : a survey of the present technology
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T07%3A45%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Quantitative%20PCR%20:%20a%20survey%20of%20the%20present%20technology&rft.jtitle=Molecular%20biotechnology&rft.au=REISCHL,%20U&rft.date=1995-02-01&rft.volume=3&rft.issue=1&rft.spage=55&rft.epage=71&rft.pages=55-71&rft.issn=1073-6085&rft.eissn=1559-0305&rft.coden=MLBOEO&rft_id=info:doi/10.1007/BF02821335&rft_dat=%3Cproquest_cross%3E77380388%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c306t-a2d4578d5d6ccdb83c2fc33244263aaf8e929586c0a7b41eab2624e95f10bd593%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=77380388&rft_id=info:pmid/7606505&rfr_iscdi=true