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mRNA analysis of single living cells

Analysis of specific gene expression in single living cells may become an important technique for cell biology. So far, no method has been available to detect mRNA in living cells without killing or destroying them. We have developed here a novel method to examine gene expression of living cells usi...

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Detalles Bibliográficos
Autores principales: Osada, Toshiya, Uehara, Hironori, Kim, Hyonchol, Ikai, Atsushi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC151804/
https://www.ncbi.nlm.nih.gov/pubmed/12646067
http://dx.doi.org/10.1186/1477-3155-1-2
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author Osada, Toshiya
Uehara, Hironori
Kim, Hyonchol
Ikai, Atsushi
author_facet Osada, Toshiya
Uehara, Hironori
Kim, Hyonchol
Ikai, Atsushi
author_sort Osada, Toshiya
collection PubMed
description Analysis of specific gene expression in single living cells may become an important technique for cell biology. So far, no method has been available to detect mRNA in living cells without killing or destroying them. We have developed here a novel method to examine gene expression of living cells using an atomic force microscope (AFM). AFM tip was inserted into living cells to extract mRNAs. The obtained mRNAs were analyzed with RT-PCR, nested PCR, and quantitative PCR. This method enabled us to examine time-dependent gene expression of single living cells without serious damage to the cells.
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spelling pubmed-1518042003-03-21 mRNA analysis of single living cells Osada, Toshiya Uehara, Hironori Kim, Hyonchol Ikai, Atsushi J Nanobiotechnology Research Analysis of specific gene expression in single living cells may become an important technique for cell biology. So far, no method has been available to detect mRNA in living cells without killing or destroying them. We have developed here a novel method to examine gene expression of living cells using an atomic force microscope (AFM). AFM tip was inserted into living cells to extract mRNAs. The obtained mRNAs were analyzed with RT-PCR, nested PCR, and quantitative PCR. This method enabled us to examine time-dependent gene expression of single living cells without serious damage to the cells. BioMed Central 2003-02-14 /pmc/articles/PMC151804/ /pubmed/12646067 http://dx.doi.org/10.1186/1477-3155-1-2 Text en Copyright © 2003 Osada et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research
Osada, Toshiya
Uehara, Hironori
Kim, Hyonchol
Ikai, Atsushi
mRNA analysis of single living cells
title mRNA analysis of single living cells
title_full mRNA analysis of single living cells
title_fullStr mRNA analysis of single living cells
title_full_unstemmed mRNA analysis of single living cells
title_short mRNA analysis of single living cells
title_sort mrna analysis of single living cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC151804/
https://www.ncbi.nlm.nih.gov/pubmed/12646067
http://dx.doi.org/10.1186/1477-3155-1-2
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