Gene Knock down (RNAi) |
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RNA interference (RNAi) is a mechanism in which double-stranded RNAs inhibits corresponding gene expression by inducing degradation of its mRNA.
RNAi approaches have become state-of-the-art methods for in vitro target validation.
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Invitrogen Corporation and genOway are working together to provide
a complete RNAi solutions platform for the in vivo use of shRNA to researchers worldwide
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genOway has developed a panel of technologies that secures in vivo gene Knock-down. |
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Random insertion of the shRNA construct into the mouse genome |
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shRNA copy number is controlled |
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Access to high numbers of founders to avoid shRNA position effects |
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Short development time (similar to DNA microinjection) |
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The offer genOway has developed can include the following steps, but the service is flexible (can be limited to part of this offer and/or adapted to customer requirements) |
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| Step 1 : |
Construction of the shRNA expression vector |
| Step 2 : |
Random integration of the shRNA expression vector |
| Step 3 : |
Blastocyst injection and chimera generation |
| Step 4 : |
Breeding to the F1 and F2 generation |
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Targeted insertion of the shRNA construct into the mouse genome |
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The " Safe in vivo RNAi" technology enables a targeted insertion (knock-in) of the shRNA construct and secures its expression: |
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Access to ready-to-use targeting vectors suitable for spatio-temporal control of shRNA expression |
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For in vivo validation of shRNA and relevant comparative studies |
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The target gene can be subsequently removed to study shRNA off-target effects. |
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The offer genOway has developed can include the following steps, but the service is flexible (can be limited to part of this offer and/or adapted to customer requirements) |
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| Step 1 : |
Insertion of the shRNA of interest into genOway ready-to-use knock-in vector |
| Step 2 : |
Homologous recombination in Embryonic Stem cells (ES Cell) |
| Step 3 : |
Blastocyst injection and chimera generation |
| Step 4 : |
Breeding to the F1 and F2 generation |
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