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A Homogeneous HLA-B*27 Genotyping Assay Using Dried Reagent Mixtures
The presence of HLA-B*27 allele with patients suspected with ankylosing spondylitis can be used in the diagnostic process. We have developed an assay for typing for the HLA-B*27 in whole blood dried on sample collection cards using pre-dried reagent wells and homogeneous time-resolved fluorescence b...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835278/ https://www.ncbi.nlm.nih.gov/pubmed/19893203 http://dx.doi.org/10.3233/DMA-2009-0653 |
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author | Kiviniemi, Minna Ilonen, Jorma Lövgren, Timo |
author_facet | Kiviniemi, Minna Ilonen, Jorma Lövgren, Timo |
author_sort | Kiviniemi, Minna |
collection | PubMed |
description | The presence of HLA-B*27 allele with patients suspected with ankylosing spondylitis can be used in the diagnostic process. We have developed an assay for typing for the HLA-B*27 in whole blood dried on sample collection cards using pre-dried reagent wells and homogeneous time-resolved fluorescence based PCR approach. Essentially only the sample needs to be added to the dry ready-to-use reaction well in order to start the homogenous amplification assay. The method was validated with 229 samples also typed with an existing DELFIA-based method and results of both assays were 100% concordant. The dried reagents were shown to be stable at least up to eight weeks at room temperature without any decline in their performance. |
format | Online Article Text |
id | pubmed-3835278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38352782013-12-02 A Homogeneous HLA-B*27 Genotyping Assay Using Dried Reagent Mixtures Kiviniemi, Minna Ilonen, Jorma Lövgren, Timo Dis Markers Other The presence of HLA-B*27 allele with patients suspected with ankylosing spondylitis can be used in the diagnostic process. We have developed an assay for typing for the HLA-B*27 in whole blood dried on sample collection cards using pre-dried reagent wells and homogeneous time-resolved fluorescence based PCR approach. Essentially only the sample needs to be added to the dry ready-to-use reaction well in order to start the homogenous amplification assay. The method was validated with 229 samples also typed with an existing DELFIA-based method and results of both assays were 100% concordant. The dried reagents were shown to be stable at least up to eight weeks at room temperature without any decline in their performance. IOS Press 2009 2009-11-05 /pmc/articles/PMC3835278/ /pubmed/19893203 http://dx.doi.org/10.3233/DMA-2009-0653 Text en Copyright © 2009 Hindawi Publishing Corporation. |
spellingShingle | Other Kiviniemi, Minna Ilonen, Jorma Lövgren, Timo A Homogeneous HLA-B*27 Genotyping Assay Using Dried Reagent Mixtures |
title | A Homogeneous HLA-B*27 Genotyping Assay Using Dried Reagent Mixtures |
title_full | A Homogeneous HLA-B*27 Genotyping Assay Using Dried Reagent Mixtures |
title_fullStr | A Homogeneous HLA-B*27 Genotyping Assay Using Dried Reagent Mixtures |
title_full_unstemmed | A Homogeneous HLA-B*27 Genotyping Assay Using Dried Reagent Mixtures |
title_short | A Homogeneous HLA-B*27 Genotyping Assay Using Dried Reagent Mixtures |
title_sort | homogeneous hla-b*27 genotyping assay using dried reagent mixtures |
topic | Other |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835278/ https://www.ncbi.nlm.nih.gov/pubmed/19893203 http://dx.doi.org/10.3233/DMA-2009-0653 |
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