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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-269304
- DOI to cite this document:
- 10.5283/epub.26930
Alternative links to fulltext:Pubmed
Abstract
The aim of the present study was to set up a method to quantify renin mRNA levels in mouse renal juxtaglomerular cells, the main physiological site of renin synthesis. Because of the scarcity of the cells, a quantitative polymerase chain reaction had to be developed to measure renin mRNA. Juxtaglomerular cells were isolated and cultured for 2 days under various conditions, and renin mRNA was ...

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