CRISPR for Transcriptional Activation and Repression Several research groups have harnessed the specificity and easy re-programmability of the CRISPR/Cas9 system to create targetable CRISPR/Cas9 ribonucleoprotein......
CRISPR/Cas9基因编辑系统主要由靶向目标基因序列的gRNA和切割DNA双链的Cas9蛋白组成。......
A Guide to CRISPR /Cas9 Delivery: How to Maximize Your Editing Efficiency While CRISPR/Cas9 editing is utilized in a wide variety of cell types, editing efficiency continues to pose a challenge to researchers......
CRISPR/Cas9 technology for precise gene editing has already proven successful in other species including in mice, C. elegans, Xenopus tropicalis, and plants.......
Briefly, targeting of the Cas9 nuclease to specific genomic sequences depends on the guide RNA and particularly a 20 nucleotide sequence, which interacts with the DNA at the target site.......
Lumeng Ye, R&D Senior Scientist, leads the design and synthesis of ssDNA for non-viral DNA CRISPR/Cas9 gene-editing applications.......
Please Select T cell engineering with Lentivirus vectors T cell engineering with CRISPR/Cas9 and AAV vectors Fully Non-viral T cell engineering Unsure Are you interested in viral or non-viral T cell engineering
No caminho para imunoterapias não virais de células T Obtenha o novo cartaz de GenScript As imunoterapias de células T têm conseguido respostas duradouras em tumores malignos hematológicos e prometem
Using CRISPR Libraries for Screening Pooled CRISPR guide RNA libraries, or gRNA libraries, are ideal for high-throughput screening of important molecular targets. These libraries leverage the efficien
Avanzamento verso le immunoterapie a cellule T non virali Ottieni il nuovo poster di GenScript Le immunoterapie con cellule T hanno ottenuto risposte a lungo termine nelle neoplasie ematologiche e pro