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PMID: 9778453 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Semi-quantitative RT-PCR for comparison of mRNAs in cells with different amounts of housekeeping gene transcripts.

Molecular and cellular probes ·Vol. 12 ·No. 5 ·1998-10-00 ·Pages 283-91

Serazin-Leroy V, Denis-Henriot D, Morot M, de Mazancourt P, Giudicelli Y

Abstract

A simple method is reported here for the semi-quantitative assay of mRNAs in the presence of an exogenous mRNA (pBR322 transcript) as a standard. This method uses the co-reverse transcription and co-amplification (co RT-PCR) of the target and standard mRNAs. This procedure enables transcripts to be compared when the differentiation process affects the transcription pattern of the beta-actin housekeeping gene, a commonly used internal standard. This method is sensitive and avoids constructing internal competitive RNA standards. As an example, it is shown that beta-actin transcription decreases and type V adenylyl cyclase transcription increases in adipocytes, when compared to preadipocytes.

MeSH Terms
Actins/genetics Adipocytes/cytology,metabolism Animals Cells, Cultured DNA Primers DNA, Complementary Epididymis Male Plasmids Quality Control RNA, Messenger/analysis,genetics Rats Rats, Sprague-Dawley Reproducibility of Results Reverse Transcriptase Polymerase Chain Reaction/methods,standards Transcription, Genetic
Chemicals
Actins DNA Primers DNA, Complementary RNA, Messenger
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Serazin-Leroy V
Laboratoire de Biochimie de la Faculté de Médecine Paris-Ouest, INSERM CJF 94-02, Université René, Descartes Paris V, France.
Denis-Henriot D
Morot M
de Mazancourt P
Giudicelli Y
Article Info
Journal
Molecular and cellular probes
Abbr.
Mol Cell Probes
ISSN
0890-8508
Published
1998-10-00
Pages
283-91
Language
English
Region
England
NLM ID
8709751
Subset
IM
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