CRISPR Mouse Deletion SL4

Get tips on using Edit-R CRISPR-Cas9 Nuclease Expression Plasmid to perform CRISPR Mouse - Repression XylT2

The RNA-guided CRISPR-Cas9 nuclease system has revolutionized the genome editing practices. For the most part, the Cas9-mediated genome editing is performed either via nonhomologous end joining (NHEJ) or homology-directed repair (HDR) in mammalian cells, However, designing of specific sgRNAs and minimizing off-target cleavage mediated mutagenesis are the major challenges in CRISPR-Cas based genome editing. To circumvent these issues, we can take advantages of many available tools and approaches for sgRNA construction and delivery.

The RNA-guided CRISPR-Cas9 nuclease system has revolutionized the genome editing practices. For the most part, the Cas9-mediated genome editing is performed either via nonhomologous end joining (NHEJ) or homology-directed repair (HDR) in mammalian cells, However, designing of specific sgRNAs and minimizing off-target cleavage mediated mutagenesis are the major challenges in CRISPR-Cas based genome editing. To circumvent these issues, we can take advantages of many available tools and approaches for sgRNA construction and delivery.

Get tips on using lentiCRISPR v2 to perform CRISPR Human - Deletion CD38

Get tips on using lentiGuide-Puro to perform CRISPR Human - Deletion CLK1

Get tips on using pLX-sgRNA to perform CRISPR Human - Deletion CIITA

Get tips on using lentiCRISPR v2 to perform CRISPR Human - Deletion AXL

Get tips on using lentiCRISPR v2 to perform CRISPR Human - Deletion NGRN

Get tips on using lentiCRISPR v2 to perform CRISPR Human - Deletion SST3B

Get tips on using lentiCRISPR v2 to perform CRISPR Human - Deletion SST3A