Subventions et des contributions :

Titre :
Validation of functionalized transcription factors as a novel cell culture supplements
Numéro de l’entente :
CRDPJ
Valeur d'entente :
100 000,00 $
Date d'entente :
13 déc. 2017 -
Organisation :
Conseil de recherches en sciences naturelles et en génie du Canada
Location :
Colombie-Britannique, Autre, CA
Numéro de référence :
GC-2017-Q3-00364
Type d'entente :
subvention
Type de rapport :
Subventions et des contributions
Informations supplémentaires :

Subvention ou bourse octroyée s'appliquant à plus d'un exercice financier (2017-2018 à 2019-2020).

Nom légal du bénéficiaire :
Willerth, Stephanie (University of Victoria)
Programme :
Subventions de recherche et développement coopérative - projet
But du programme :

The market for cell culture media and supplements is estimated to be $6 billion per year as reported by Global Industry Analysts Inc. The overall goal of this project is to validate novel protein therapeutics consisting of transcription factors functionalized with a novel intracellular protein delivery technology developed by iProgen Biotech for use as cell culture supplements. This project represents a continuation of a successful collaboration between Dr. Stephanie Willerth, a Canada Research Chair in Biomedical Engineering and Associate Professor of Biomedical Engineering at the University of Victoria, and the biotechnology company - iProgen Biotech. Our previous collaboration validated a novel protein therapeutic called IASCL1 for use as a cell culture supplement that promoted the differentiation of human induced pluripotent stem cells into neurons, which are cells found in the central nervous system. We also have promising preliminary data that IASCL can directly reprogram skin cells called fibroblasts into neuron-like cells. This project will further characterize ability of IASCL1 to reprogram fibroblasts into neurons as well as characterize the effects of other novel transcription factors, including ISOX2, IBRN2, IMYT1L, and INGN2, on the reprogramming process.x000D
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