General Method for HPLC Purification and Sequencing of Selected dsDNA Gene Fragments from Complex PCRs Generated during Gene Expression Profiling

Gene expression profiling using an AFLP-based technique generates a large number of gene fragments that require identification by sequencing. The DNA fragments vary in length from about 50–500 bp. Ion-pair reversed-phase HPLC can be used to purify selected double-stranded DNA fragments that represen...

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Main Authors: L.Y. Wong, V. Belonogoff, V.L. Boyd, N.M. Hunkapiller, P.M. Casey, S.-N. Liew, K.D. Lazaruk, S. Baumhueter
Format: Article
Language:English
Published: Taylor & Francis Group 2000-04-01
Series:BioTechniques
Online Access:https://www.future-science.com/doi/10.2144/00284rr07
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author L.Y. Wong
V. Belonogoff
V.L. Boyd
N.M. Hunkapiller
P.M. Casey
S.-N. Liew
K.D. Lazaruk
S. Baumhueter
author_facet L.Y. Wong
V. Belonogoff
V.L. Boyd
N.M. Hunkapiller
P.M. Casey
S.-N. Liew
K.D. Lazaruk
S. Baumhueter
author_sort L.Y. Wong
collection DOAJ
description Gene expression profiling using an AFLP-based technique generates a large number of gene fragments that require identification by sequencing. The DNA fragments vary in length from about 50–500 bp. Ion-pair reversed-phase HPLC can be used to purify selected double-stranded DNA fragments that represent differentially expressed genes. The gene fragments are sequenced directly after vacuum drying of the collected HPLC fractions.
format Article
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issn 0736-6205
1940-9818
language English
publishDate 2000-04-01
publisher Taylor & Francis Group
record_format Article
series BioTechniques
spelling doaj-art-a453f7e63db74282a0f70588554d0d5f2025-08-20T02:25:53ZengTaylor & Francis GroupBioTechniques0736-62051940-98182000-04-0128477678310.2144/00284rr07General Method for HPLC Purification and Sequencing of Selected dsDNA Gene Fragments from Complex PCRs Generated during Gene Expression ProfilingL.Y. Wong0V. Belonogoff1V.L. Boyd2N.M. Hunkapiller3P.M. Casey4S.-N. Liew5K.D. Lazaruk6S. Baumhueter71Celera Genomics, Foster City, CA, USA1Celera Genomics, Foster City, CA, USA1Celera Genomics, Foster City, CA, USA1Celera Genomics, Foster City, CA, USA1Celera Genomics, Foster City, CA, USA1Celera Genomics, Foster City, CA, USA1Celera Genomics, Foster City, CA, USA1Celera Genomics, Foster City, CA, USAGene expression profiling using an AFLP-based technique generates a large number of gene fragments that require identification by sequencing. The DNA fragments vary in length from about 50–500 bp. Ion-pair reversed-phase HPLC can be used to purify selected double-stranded DNA fragments that represent differentially expressed genes. The gene fragments are sequenced directly after vacuum drying of the collected HPLC fractions.https://www.future-science.com/doi/10.2144/00284rr07
spellingShingle L.Y. Wong
V. Belonogoff
V.L. Boyd
N.M. Hunkapiller
P.M. Casey
S.-N. Liew
K.D. Lazaruk
S. Baumhueter
General Method for HPLC Purification and Sequencing of Selected dsDNA Gene Fragments from Complex PCRs Generated during Gene Expression Profiling
BioTechniques
title General Method for HPLC Purification and Sequencing of Selected dsDNA Gene Fragments from Complex PCRs Generated during Gene Expression Profiling
title_full General Method for HPLC Purification and Sequencing of Selected dsDNA Gene Fragments from Complex PCRs Generated during Gene Expression Profiling
title_fullStr General Method for HPLC Purification and Sequencing of Selected dsDNA Gene Fragments from Complex PCRs Generated during Gene Expression Profiling
title_full_unstemmed General Method for HPLC Purification and Sequencing of Selected dsDNA Gene Fragments from Complex PCRs Generated during Gene Expression Profiling
title_short General Method for HPLC Purification and Sequencing of Selected dsDNA Gene Fragments from Complex PCRs Generated during Gene Expression Profiling
title_sort general method for hplc purification and sequencing of selected dsdna gene fragments from complex pcrs generated during gene expression profiling
url https://www.future-science.com/doi/10.2144/00284rr07
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