Genetic Engineering Innovations - DNA-RNA Platforms GEG Tech
GEG Tech. GEG Tech establishes research programs using its platform with academic and industrial groups for fundamental research and...
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Genetic Engineering Innovations - DNA-RNA Platforms GEG Tech
GEG Tech establishes research programs using its platform with academic and industrial groups for fundamental research and early-stage therapeutic development.
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Frequently asked questions about our products and services
What kind of products does the catalog offer? For what kind of applications can lentiviral vectors be used? Which cell type can be transduced? What is the On-Demand Service? Is the On-Demand service "...
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Frequently asked questions about our products and services
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Live tracking of HIV-1 based lentiviral vectors - GEG Tech
Technology breakthrough: visualization of lentivirus genomes in living cells using ANCHOR technology.
Geg-tech.com news digest
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5 years
The CAR T-Cells Revolution has begun
These past few months, cancer immunotherapy has sped-up thanks to CAR technology. One look at the recent news about this is enough to figure that out. As examples:
Two major deals between pharmaceutical companies and biotechs specialized in CAR T-cells: Gilead bought Kite Pharma for $12 billion, and Celgene bought Juno Therapeutics for $9 billion.... -
6 years
Live tracking of HIV-1 based lentiviral vectors
First-ever live tracking of HIV-1 based lentiviral vectors in human cells
Technology breakthrough: visualization of lentivirus genomes in living cells using ANCHOR technology.
We are proud to announce that we obtain great results through a collaborative project with NeoVirTech, a company developing auto fluorescent virus for imaging and screening applications. GEG Tech has validated the auto-fluorescent ANCHOR tagging of lentiviral... -
6 years
Self-Inactivating KamiCas9 System
The Self-Inactivating KamiCas9 System for the Editing of CNS Disease Genes
In this article, Merienne et al. designed a smart lentiviral vector system to improve the safety for genome editing of CNS disease gene. They characterized their CRISPR self-inactivating system (KamiCas9) for permanent disruption of huntingtin gene in... -
6 years
Preclinical Evaluation of a Lentiviral Vector
Preclinical Evaluation of a Lentiviral Vector for Huntingtin Silencing
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder resulting from a polyglutamine expansion in the huntingtin (HTT) protein. There is currently no cure for this disease, but recent studies suggest that RNAi to downregulate...
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