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Development of Competitive mRNA PCR for the Quantification of Interleukin-6-Responsive junB Oncogene Expression
Author(s) -
Péter Igaz,
György Fejér,
Csaba Szalai,
Sára Tóth,
András Falus
Publication year - 1998
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/98245rr02
Subject(s) - junb , biology , messenger rna , microbiology and biotechnology , gene expression , oncogene , interleukin 1β , interleukin , genetics , computational biology , gene , cytokine , cell cycle
The transcription factor junB belongs to the jun family of protooncogenes. The appearance of junB mRNA in hepatic cells is an extremely early and sensitive marker of the action of proinflammatory cytokines including interleukin-6. In this study, a competitive reverse transcription (RT)-PCR assay has been developed that is suitable for the quantitative determination of junB mRNA expression. This nonisotopic assay compared to other methods (e.g., Northern blot) is a fast and convenient way to determine the expression of the junB gene and thus the immediate concentration- and time-dependent action of interleukin-6. Because interleukin-6 and interleukin-6-type cytokines play a highly important regulatory role in various pathophysiologically important processes, such as hepatic acute-phase reaction, the quantitative assay of junB mRNA completes the scale of laboratory approaches in inflammation and among other pathological conditions.

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