Quantitation of infectious human immunodeficiency virus using a modified plaque forming assay
This report describes a modified plaque forming assay which has been used for quantitation of infectious human immunodeficiency virus (HIV) in cell culture supernatant fluid. The number of infectious units determined by the plaque assay correlates closely with the 50% infectious dose determined by a...
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Veröffentlicht in: | Journal of virological methods 1988-12, Vol.22 (2), p.303-308 |
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creator | Kiernan, R.E. McPhee, D.A. Doherty, R.R. |
description | This report describes a modified plaque forming assay which has been used for quantitation of infectious human immunodeficiency virus (HIV) in cell culture supernatant fluid. The number of infectious units determined by the plaque assay correlates closely with the 50% infectious dose determined by a conventional assay in cell culture. In contrast, particle associated reverse transcriptase (RT) activity correlates poorly with the amount of infectious HIV present in culture supernatant fluids. |
doi_str_mv | 10.1016/0166-0934(88)90112-7 |
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The number of infectious units determined by the plaque assay correlates closely with the 50% infectious dose determined by a conventional assay in cell culture. In contrast, particle associated reverse transcriptase (RT) activity correlates poorly with the amount of infectious HIV present in culture supernatant fluids.</description><identifier>ISSN: 0166-0934</identifier><identifier>EISSN: 1879-0984</identifier><identifier>DOI: 10.1016/0166-0934(88)90112-7</identifier><identifier>PMID: 2464609</identifier><identifier>CODEN: JVMEDH</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>AIDS/HIV ; Biological and medical sciences ; Cell Line ; Cytopathogenic Effect, Viral ; Fundamental and applied biological sciences. 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The number of infectious units determined by the plaque assay correlates closely with the 50% infectious dose determined by a conventional assay in cell culture. In contrast, particle associated reverse transcriptase (RT) activity correlates poorly with the amount of infectious HIV present in culture supernatant fluids.</description><subject>AIDS/HIV</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Cytopathogenic Effect, Viral</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>HIV</subject><subject>HIV - enzymology</subject><subject>HIV - growth & development</subject><subject>HIV - isolation & purification</subject><subject>human immunodeficiency virus</subject><subject>Humans</subject><subject>Microbiology</subject><subject>Plaque assay</subject><subject>Quantitation</subject><subject>RNA-Directed DNA Polymerase - analysis</subject><subject>Techniques used in virology</subject><subject>Viral Plaque Assay</subject><subject>Virology</subject><issn>0166-0934</issn><issn>1879-0984</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkVtLHTEUhUOx2KPtP1DIgxT7MDaZ3F8EEa0FQQT7WEImF02ZyZwmMwfOv2_OhfNYH0JI1tpr73wB4AyjK4ww_14Xb5Ai9FLKbwph3DbiA1hgKVS9lvQILA6WT-CklD8IISYIOQbHLeWUI7UAv59nk6Y4mSmOCY4BxhS8rYe5wLd5MAnGYZjT6HyINvpk13AVcxXnEtMrNHAYXQzRO7jszd_ZwzDmYauUYtafwcdg-uK_7PdT8Ov-7uX2oXl8-vHz9uaxsRSLqTGubQXtjOKdRALhlmDmCTEYicA7Z7lyqrUMWaWoF66zDDvSWWWYooQFR07B113uMo91iDLpIRbr-94kX1-iheRMSoXfNWJWmxNJqpHujDaPpWQf9DLHweS1xkhv8OsNW71hq6XUW_xa1LLzff7cDd4diva8q36x102xpg_ZJBvLwSZa1hK-ibne2XyFtoo-67KF713M9Xe0G-P_5_gHBCGh1w</recordid><startdate>19881201</startdate><enddate>19881201</enddate><creator>Kiernan, R.E.</creator><creator>McPhee, D.A.</creator><creator>Doherty, R.R.</creator><general>Elsevier B.V</general><general>Elsevier</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>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19881201</creationdate><title>Quantitation of infectious human immunodeficiency virus using a modified plaque forming assay</title><author>Kiernan, R.E. ; McPhee, D.A. ; Doherty, R.R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-ad2274ba96b807012315e33a107f6bdc69d92c50c994e7dbc51d3bc9a59435fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>AIDS/HIV</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Cytopathogenic Effect, Viral</topic><topic>Fundamental and applied biological sciences. 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The number of infectious units determined by the plaque assay correlates closely with the 50% infectious dose determined by a conventional assay in cell culture. In contrast, particle associated reverse transcriptase (RT) activity correlates poorly with the amount of infectious HIV present in culture supernatant fluids.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>2464609</pmid><doi>10.1016/0166-0934(88)90112-7</doi><tpages>6</tpages></addata></record> |
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subjects | AIDS/HIV Biological and medical sciences Cell Line Cytopathogenic Effect, Viral Fundamental and applied biological sciences. Psychology HIV HIV - enzymology HIV - growth & development HIV - isolation & purification human immunodeficiency virus Humans Microbiology Plaque assay Quantitation RNA-Directed DNA Polymerase - analysis Techniques used in virology Viral Plaque Assay Virology |
title | Quantitation of infectious human immunodeficiency virus using a modified plaque forming assay |
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