A Rapid Direct Telomerase Assay Method Using 96-Well Streptavidin Plates

We have developed a high-throughput direct assay method for the assay of telomerase activity that improves on previous direct telomerase assays in two ways that allow larger numbers of samples to be conveniently processed: (i) 96-well streptavidin coated plates are used to bind and wash biotinylated...

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Main Authors: Rawle Francis, Simon H. Friedman
Format: Article
Language:English
Published: Taylor & Francis Group 2002-05-01
Series:BioTechniques
Online Access:https://www.future-science.com/doi/10.2144/02325dd05
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author Rawle Francis
Simon H. Friedman
author_facet Rawle Francis
Simon H. Friedman
author_sort Rawle Francis
collection DOAJ
description We have developed a high-throughput direct assay method for the assay of telomerase activity that improves on previous direct telomerase assays in two ways that allow larger numbers of samples to be conveniently processed: (i) 96-well streptavidin coated plates are used to bind and wash biotinylated primer extension products from the telomerase assay, as opposed to tubes containing streptavidin-coated magnetic beads; and (ii) storage phosphorimagery is used instead of film autoradiography to detect telomerase products after being washed and released from the streptavidin- derivatized matrix. This method improves on previous direct assay methods using magnetic beads by allowing larger numbers of samples to be conveniently assayed. Also, the total activity of the radiolabeled nucleotides used in this procedure is significantly lower than that used in standard direct telomerase assays, lowering costs and exposure to radioactivity. We have validated the assay by repeating, in triplicate, the IC50 determination of rivanol, our previously identified telomerase inhibitor.
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spelling doaj-art-7400c58a3a10486e99afc60afc70cd5c2025-08-20T02:26:03ZengTaylor & Francis GroupBioTechniques0736-62051940-98182002-05-013251154116010.2144/02325dd05A Rapid Direct Telomerase Assay Method Using 96-Well Streptavidin PlatesRawle Francis0Simon H. Friedman11University of Missouri, Kansas City, MO, USA1University of Missouri, Kansas City, MO, USAWe have developed a high-throughput direct assay method for the assay of telomerase activity that improves on previous direct telomerase assays in two ways that allow larger numbers of samples to be conveniently processed: (i) 96-well streptavidin coated plates are used to bind and wash biotinylated primer extension products from the telomerase assay, as opposed to tubes containing streptavidin-coated magnetic beads; and (ii) storage phosphorimagery is used instead of film autoradiography to detect telomerase products after being washed and released from the streptavidin- derivatized matrix. This method improves on previous direct assay methods using magnetic beads by allowing larger numbers of samples to be conveniently assayed. Also, the total activity of the radiolabeled nucleotides used in this procedure is significantly lower than that used in standard direct telomerase assays, lowering costs and exposure to radioactivity. We have validated the assay by repeating, in triplicate, the IC50 determination of rivanol, our previously identified telomerase inhibitor.https://www.future-science.com/doi/10.2144/02325dd05
spellingShingle Rawle Francis
Simon H. Friedman
A Rapid Direct Telomerase Assay Method Using 96-Well Streptavidin Plates
BioTechniques
title A Rapid Direct Telomerase Assay Method Using 96-Well Streptavidin Plates
title_full A Rapid Direct Telomerase Assay Method Using 96-Well Streptavidin Plates
title_fullStr A Rapid Direct Telomerase Assay Method Using 96-Well Streptavidin Plates
title_full_unstemmed A Rapid Direct Telomerase Assay Method Using 96-Well Streptavidin Plates
title_short A Rapid Direct Telomerase Assay Method Using 96-Well Streptavidin Plates
title_sort rapid direct telomerase assay method using 96 well streptavidin plates
url https://www.future-science.com/doi/10.2144/02325dd05
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