Rapid quantitation of gene therapy specific CFTR expression using the amplification refractory mutation system

Gene therapy offers the potential of correcting genetic disorders such as cystic fibrosis (CF). By complementing the non-functional endogenous cystic fibrosis transmembrane conductance regulator (CFTR) gene with a functional transgene, we anticipate it may alleviate the disease phenotype. All approa...

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Veröffentlicht in:BioTechniques. - 1993. - 27(1999), 1 vom: 01. Juli, Seite 122-6
1. Verfasser: Thorpe, P H (VerfasserIn)
Weitere Verfasser: Porteous, D J
Format: Aufsatz
Sprache:English
Veröffentlicht: 1999
Zugriff auf das übergeordnete Werk:BioTechniques
Schlagworte:Journal Article Research Support, Non-U.S. Gov't CFTR protein, human DNA Primers DNA, Complementary RNA, Messenger Cystic Fibrosis Transmembrane Conductance Regulator 126880-72-6
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245 1 0 |a Rapid quantitation of gene therapy specific CFTR expression using the amplification refractory mutation system 
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520 |a Gene therapy offers the potential of correcting genetic disorders such as cystic fibrosis (CF). By complementing the non-functional endogenous cystic fibrosis transmembrane conductance regulator (CFTR) gene with a functional transgene, we anticipate it may alleviate the disease phenotype. All approaches to CF gene therapy rely upon sensitive assays to monitor delivery, expression and maintenance of CFTR vectors. Here, we describe the adaptation of the amplification refractory mutation system (ARMS) to discriminate between different forms of CFTR. A LightCycler PCR machine allows realtime continuous fluorescence monitoring of rapid-cycle PCR. We show quantitation of and discrimination between expression of endogenous (wild-type or mutant) CFTR and the introduced transgene 
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650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a DNA Primers  |2 NLM 
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