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Suppression of Caspase-3 Expression Using the psiSTRIKE™ hMGFP Vector

Jolanta Vidugiriene, Ph.D., Thomas Yeager, Ph.D., Cheryl Bailey, Ph.D., Cindy Sprecher, B.S., Bob Bulleit, Ph.D., and Doug Storts, Ph.D.
Promega Corporation

The siSTRIKE™ U6 Hairpin Cloning System—hMGFP includes a short hairpin RNA expression vector for the production of short interfering RNAs. This vector contains an internal fluorescent marker, the Monster Green™ Fluorescent Protein (hMGFP), to monitor the cellular delivery of these shRNA constructs. This psiSTRIKE™ hMGFP Vector allows fast and reliable cloning of hairpin target sequences. The presence of the hMGFP gene enables transfection efficiency to be determined easily and facilitates selection of transfected cells by fluorescence-activated cell sorting (FACS®). Importantly, the expression of hMGFP does not affect gene silencing by shRNA molecules expressed from the same vector. In this article, we demonstrate efficient suppression of caspase-3 gene expression using the psiSTRIKE™ hMGFP Vector.

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Promega Notes 88 (2004) 16–19: Request this issue.
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