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Article type: Research Article
Authors: Dahlstrøm, Berit | Esbensen, Ying | Blom, Peter | Bukholm, Geir
Affiliations: Department of Obstetrics and Gynecology, Akershus University Hospital, Lørenskog, Norway | Institute of Clinical Epidemiology and Molecular Biology, Akershus University Hospital, Lørenskog, Norway | Department of Pathology, Faculty Division Akershus University Hospital, University of Oslo, N-1478 Lørenskog, Norway
Note: [] Corresponding author: Berit Dahlstrøm, Department of Obstetrics and Gynecology, Akershus University Hospital, P.B.24 Ahus, N-1478 Lørenskog, Norway. Tel.: +47 91694411; E-mail: [email protected]
Abstract: The aim of this study was to develop an assay method for determination of down stream gene expression in endothelial cells from human decidual tissue preserved in an RNA-conserving buffer. Human decidual tissue was collected and preserved in RNAlater. The tissue samples were dissected and passed through a mechanical tissue disaggregator, incubated with CD31-coated paramagnetic beads and the attached cells were extracted. RNA isolated from the enriched cells proved to be conserved with good quality and a genome RNA-microarray was successfully performed. The method provides an alternative for studying in vivo gene expression in endothelial cells from human decidual tissue.
Keywords: HEEC, endothelial cells, in vivo gene expression, cell isolation, RNA degradation
Journal: Journal of Neonatal-Perinatal Medicine, vol. 1, no. 4, pp. 245-251, 2008
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