dna-methylation-profiling-gene-specific-profiling-ca-ski-hpv-16

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DNA DNA isolation / purification Soil samples

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RNA siRNA / miRNA gene silencing Human HUVEC ATF4 Lipid

DNA DNA quantification Human MCF10A

DNA DNA isolation / purification Viral

DNA DNA isolation / purification Insects

DNA DNA isolation / purification Fish

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.

DNA CRISPR Human Repression HBV

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Get tips on using E-Gel™ 50 bp DNA Ladder to perform DNA Ladder 50 bp

Products Thermo Fisher Scientific E-Gel™ 50 bp DNA Ladder

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