Efficiency of two different transfection reagents for use with human NTERA2 cells

The teratocarcinoma cell line NTERA2 is recently used in a wide range of researches (from developmental biology to toxicology, for their ability to be induced to neural differentiation. In order to study the genetic potential of these cells, it is needed to use methods for gene silencing and/or mRNA...

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Main Authors: MG Aluigi, S Hofreiter, C Falugi, M Pestarino, S Candiani
Format: Article
Language:English
Published: PAGEPress Publications 2009-08-01
Series:European Journal of Histochemistry
Online Access:http://www.ejh.it/index.php/ejh/article/view/1155
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spelling doaj-ede04ebc3e8248b9b195393c2d6e568d2020-11-25T03:41:43ZengPAGEPress PublicationsEuropean Journal of Histochemistry 1121-760X2038-83062009-08-0151430130410.4081/1155791Efficiency of two different transfection reagents for use with human NTERA2 cellsMG AluigiS HofreiterC FalugiM PestarinoS CandianiThe teratocarcinoma cell line NTERA2 is recently used in a wide range of researches (from developmental biology to toxicology, for their ability to be induced to neural differentiation. In order to study the genetic potential of these cells, it is needed to use methods for gene silencing and/or mRNA interference, allowing cell viability and further differentiation. To check these features, we simultaneously tested the transfection efficiency of NTERA2, A549 and HeLa cells with Metafectene PRO (Biontex, Germany) and another optimal transfection reagent currently used in our Laboratory, using as a reporter gene the DsRed2 vector (Clontech, Mountain View, CA). Under our culture conditions for NTERA2 and HeLa cells, Metafectene PRO transfection method was found to possess high throughput performance, that allows low concentration rate and low exposure time to excitation light source, thus reducing both toxicity and phototoxicity.http://www.ejh.it/index.php/ejh/article/view/1155
collection DOAJ
language English
format Article
sources DOAJ
author MG Aluigi
S Hofreiter
C Falugi
M Pestarino
S Candiani
spellingShingle MG Aluigi
S Hofreiter
C Falugi
M Pestarino
S Candiani
Efficiency of two different transfection reagents for use with human NTERA2 cells
European Journal of Histochemistry
author_facet MG Aluigi
S Hofreiter
C Falugi
M Pestarino
S Candiani
author_sort MG Aluigi
title Efficiency of two different transfection reagents for use with human NTERA2 cells
title_short Efficiency of two different transfection reagents for use with human NTERA2 cells
title_full Efficiency of two different transfection reagents for use with human NTERA2 cells
title_fullStr Efficiency of two different transfection reagents for use with human NTERA2 cells
title_full_unstemmed Efficiency of two different transfection reagents for use with human NTERA2 cells
title_sort efficiency of two different transfection reagents for use with human ntera2 cells
publisher PAGEPress Publications
series European Journal of Histochemistry
issn 1121-760X
2038-8306
publishDate 2009-08-01
description The teratocarcinoma cell line NTERA2 is recently used in a wide range of researches (from developmental biology to toxicology, for their ability to be induced to neural differentiation. In order to study the genetic potential of these cells, it is needed to use methods for gene silencing and/or mRNA interference, allowing cell viability and further differentiation. To check these features, we simultaneously tested the transfection efficiency of NTERA2, A549 and HeLa cells with Metafectene PRO (Biontex, Germany) and another optimal transfection reagent currently used in our Laboratory, using as a reporter gene the DsRed2 vector (Clontech, Mountain View, CA). Under our culture conditions for NTERA2 and HeLa cells, Metafectene PRO transfection method was found to possess high throughput performance, that allows low concentration rate and low exposure time to excitation light source, thus reducing both toxicity and phototoxicity.
url http://www.ejh.it/index.php/ejh/article/view/1155
work_keys_str_mv AT mgaluigi efficiencyoftwodifferenttransfectionreagentsforusewithhumanntera2cells
AT shofreiter efficiencyoftwodifferenttransfectionreagentsforusewithhumanntera2cells
AT cfalugi efficiencyoftwodifferenttransfectionreagentsforusewithhumanntera2cells
AT mpestarino efficiencyoftwodifferenttransfectionreagentsforusewithhumanntera2cells
AT scandiani efficiencyoftwodifferenttransfectionreagentsforusewithhumanntera2cells
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