siRNA / miRNA gene silencing Mouse NIH-3T3

Get tips on using BV421 Mouse Anti-Human CD27 to perform Flow cytometry Anti-bodies Human - CD27

Get tips on using PE Mouse anti-Human CD105 to perform Flow cytometry Anti-bodies Human - CD105

Get tips on using FITC Mouse Anti-Human CD71 to perform Flow cytometry Anti-bodies Human - CD71

Get tips on using APC Mouse Anti-Human CD71 to perform Flow cytometry Anti-bodies Human - CD71

Get tips on using FITC Mouse Anti-Human CD90 to perform Flow cytometry Anti-bodies Human - CD90

Get tips on using PE Mouse Anti-Human CD90 to perform Flow cytometry Anti-bodies Human - CD90

Get tips on using BV605 Mouse Anti-Human CD15 to perform Flow cytometry Anti-bodies Human - CD15

Get tips on using PE Mouse Anti-Human CD44 to perform Flow cytometry Anti-bodies Human - CD44

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 APC anti-mouse CD117 (c-kit) Antibody to perform Flow cytometry Anti-bodies Mouse - CD117/c-kit