An alternate method for DNA and RNA extraction from clotted blood

We developed an alternative method to extract DNA and RNA from clotted blood for genomic and molecular investigations. A combination of the TRIzol method and the QIAamp spin column were used to extract RNA from frozen clotted blood. Clotted blood was sonicated and then the QIAamp DNA Blood Mini Kit...

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Published in:Genetics and Molecular Research
Main Author: Zakaria Z.; Umi S.H.; Mokhtar S.S.; Mokhtar U.; Zaiharina M.Z.; Aziz A.T.A.; Hoh B.P.
Format: Article
Language:English
Published: Fundacao de Pesquisas Cientificas de Ribeirao Preto 2013
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84887342624&doi=10.4238%2f2013.February.4.4&partnerID=40&md5=9133d2e4ef54b6b1cbe8c87981147dd4
id 2-s2.0-84887342624
spelling 2-s2.0-84887342624
Zakaria Z.; Umi S.H.; Mokhtar S.S.; Mokhtar U.; Zaiharina M.Z.; Aziz A.T.A.; Hoh B.P.
An alternate method for DNA and RNA extraction from clotted blood
2013
Genetics and Molecular Research
12
1
10.4238/2013.February.4.4
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84887342624&doi=10.4238%2f2013.February.4.4&partnerID=40&md5=9133d2e4ef54b6b1cbe8c87981147dd4
We developed an alternative method to extract DNA and RNA from clotted blood for genomic and molecular investigations. A combination of the TRIzol method and the QIAamp spin column were used to extract RNA from frozen clotted blood. Clotted blood was sonicated and then the QIAamp DNA Blood Mini Kit was used for DNA extraction. Extracted DNA and RNA were adequate for gene expression analysis and copy number variation (CNV) genotyping, respectively. The purity of the extracted RNA and DNA was in the range of 1.8-2.0, determined by absorbance ratios of A260:A280. Good DNA and RNA integrity were confirmed using gel electrophoresis and automated electrophoresis. The extracted DNA was suitable for qPCR and microarrays for CNV genotyping, while the extracted RNA was adequate for gene analysis using RT-qPCR. © FUNPEC-RP.
Fundacao de Pesquisas Cientificas de Ribeirao Preto
16765680
English
Article
All Open Access; Bronze Open Access
author Zakaria Z.; Umi S.H.; Mokhtar S.S.; Mokhtar U.; Zaiharina M.Z.; Aziz A.T.A.; Hoh B.P.
spellingShingle Zakaria Z.; Umi S.H.; Mokhtar S.S.; Mokhtar U.; Zaiharina M.Z.; Aziz A.T.A.; Hoh B.P.
An alternate method for DNA and RNA extraction from clotted blood
author_facet Zakaria Z.; Umi S.H.; Mokhtar S.S.; Mokhtar U.; Zaiharina M.Z.; Aziz A.T.A.; Hoh B.P.
author_sort Zakaria Z.; Umi S.H.; Mokhtar S.S.; Mokhtar U.; Zaiharina M.Z.; Aziz A.T.A.; Hoh B.P.
title An alternate method for DNA and RNA extraction from clotted blood
title_short An alternate method for DNA and RNA extraction from clotted blood
title_full An alternate method for DNA and RNA extraction from clotted blood
title_fullStr An alternate method for DNA and RNA extraction from clotted blood
title_full_unstemmed An alternate method for DNA and RNA extraction from clotted blood
title_sort An alternate method for DNA and RNA extraction from clotted blood
publishDate 2013
container_title Genetics and Molecular Research
container_volume 12
container_issue 1
doi_str_mv 10.4238/2013.February.4.4
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-84887342624&doi=10.4238%2f2013.February.4.4&partnerID=40&md5=9133d2e4ef54b6b1cbe8c87981147dd4
description We developed an alternative method to extract DNA and RNA from clotted blood for genomic and molecular investigations. A combination of the TRIzol method and the QIAamp spin column were used to extract RNA from frozen clotted blood. Clotted blood was sonicated and then the QIAamp DNA Blood Mini Kit was used for DNA extraction. Extracted DNA and RNA were adequate for gene expression analysis and copy number variation (CNV) genotyping, respectively. The purity of the extracted RNA and DNA was in the range of 1.8-2.0, determined by absorbance ratios of A260:A280. Good DNA and RNA integrity were confirmed using gel electrophoresis and automated electrophoresis. The extracted DNA was suitable for qPCR and microarrays for CNV genotyping, while the extracted RNA was adequate for gene analysis using RT-qPCR. © FUNPEC-RP.
publisher Fundacao de Pesquisas Cientificas de Ribeirao Preto
issn 16765680
language English
format Article
accesstype All Open Access; Bronze Open Access
record_format scopus
collection Scopus
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