Get tips on using 100 bp DNA Ladder Ready to Load to perform DNA Ladder 100 bp
Get tips on using Quick-Load® 100 bp DNA Ladder to perform DNA Ladder 100 bp
Get tips on using Quick-Load® 100 bp DNA Ladder to perform DNA Ladder 100 bp
Get tips on using TriDye™ 1 kb Plus DNA Ladder to perform DNA Ladder 1 kb
Get tips on using Quick-Load® 1 kb DNA Ladder to perform DNA Ladder 1 kb
Get tips on using TrackIt™ 1 Kb Plus DNA Ladder to perform DNA Ladder 1 kb
Get tips on using GD 1Kb Plus DNA Ladder RTU Ladder to perform DNA Ladder 1 kb
Get tips on using MethylFlash Methylated DNA 5-mC Quantification Kit to perform DNA quantification Human - BJ
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 AllPrep DNA/RNA/Protein Mini Kit (50) to perform DNA isolation / purification Tissue - brain
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