Protocol of CRISPR /Cas9 mediated gene knockout in vitro and in vivo

Gene editing, also called genome editing, is a group of technologies to change the sequence of DNA in the genome. Several approaches to genome editing have been developed, including Zinc Finger, TALEN, and CRISPR/Cas9. Compared with the other gene editing tools, CRISPR/Cas9 system is faster, cheaper, more accurate, and more efficient, showing unprecedented advantages in gene therapy.

CRISPR/Cas9 premade products

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Type of Crispr
Viral vector
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spCas9
lentivirus
CBH
EGFP
FLAG
spCas9
lentivirus
CBH
mcherry
FLAG
AAV-CMV-saCas9
saCas9
AAV
CMV
Null
HA
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Genemedi has launched a comprehensive AAV packaging service combined with CRISPR/Cas9, the versatile genome-editing platform. The followings are some protocols of CRISPR /Cas9 mediated gene knockout in vitro and in vivo. For AAV CRISPR/Cas9 service, please visit: https://www.genemedi.com/i/aav-sacas9-packaging For lentivirus CRISPR/Cas9 service, please visit: https://www.genemedi.com/i/crispr-cas9-knockout-lentivirus-production-service For Adenovirus CRISPR/Cas9 service, please visit: https://www.genemedi.com/i/adenovirus-cas9-packaging CRISPR/Cas9 AAV Production-User Manual /pdf/Genemedi-AAV-Sa Cas9%20User%20Manual.pdf Recombinant Adenovirus-CRISPR/Cas9 Knockout System-User Manual https://www.genemedi.com/pdf/Genemedi-Adenovirus-crispr%20User%20Manual.pdf Recombinant Lentivirus-CRISPR/Cas9 Knockout System-User Manual /pdf/Genemedi-Lentivirus-crispr%20User%20Manual.pdf View Crispr Knowledge Base>>