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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 related products
Adeno Associated Virus (AAV) CRISPR/Cas9 Servicepdf download
Adenovirus CRISPR/Cas9 Service
Lentivirus CRISPR/Cas9 Service

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.net/i/aav-sacas9-packaging

For lentivirus CRISPR/Cas9 service, please visit:

https://www.genemedi.net/i/crispr-cas9-knockout-lentivirus-production-service

For Adenovirus CRISPR/Cas9 service, please visit:

https://www.genemedi.net/i/adenovirus-cas9-packaging

 

CRISPR/Cas9 AAV Production-User Manual

https://www.genemedi.net/pdf/Genemedi-AAV-Sa Cas9%20User%20Manual.pdf

Recombinant Adenovirus-CRISPR/Cas9 Knockout System-User Manual

https://www.genemedi.net/pdf/Genemedi-Adenovirus-crispr%20User%20Manual.pdf

Recombinant Lentivirus-CRISPR/Cas9 Knockout System-User Manual

https://www.genemedi.net/pdf/Genemedi-Lentivirus-crispr%20User%20Manual.pdf



View Crispr Knowledge Base>>

Other knowledge bases

AAV Knowledge Basepdf download
CRISPR/Cas9-gRNA system Knowledge Base
Adenovirus Knowledge Basepdf download
Transfection Knowledge Base
Lentivirus Knowledge Basepdf download
Advanced cell therapy