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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...

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Detalles Bibliográficos
Autores principales: Kiviniemi, Minna, Ilonen, Jorma, Lövgren, Timo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2009
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.
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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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