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 miRNeasy FFPE Kit to perform RNA isolation / purification Tissue - rat brain tissue
Get tips on using miRNeasy FFPE Kit to perform RNA isolation / purification Tissue - rat spleen tissue
Get tips on using miRNeasy FFPE Kit to perform RNA isolation / purification Tissue - rat kidney tissue
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - mouse lung tissue
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - mouse brain tissue
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - mouse kidney tissue
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - mouse bone tissue
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - mouse liver tissue
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - mouse muscle tissue
Fill out your contact details and receive price quotes in your Inbox
Outsource experiment