Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Human Larynx
Get tips on using miRNeasy FFPE Kit to perform RNA isolation / purification Tissue - Human Colon
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Human Duodenum
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Human Cerebellum
Get tips on using miRNeasy FFPE Kit to perform RNA isolation / purification Tissue - Human Bladder
Get tips on using pMT-hFIX/M to perform Protein Expression Eukaryotic cells - Drosophila S2 rFIX
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 RNeasy Mini Kit to perform RNA isolation / purification Cells - immortalized Raji
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Human Spinal cord
Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - Human Pituitary gland
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