siRNA / RNAi /miRNA transfection Human Cells THP-1

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Get tips on using Gibco™ DMEM, high glucose to perform Stem cell Differentiation media hMSCs differentiation into osteogenic cells

Products Fisher Scientific Gibco™ DMEM, high glucose

Get tips on using Gibco™ MEM α, Nucleosides to perform Stem cell Differentiation media hMSCs differentiation into myogenic cells

Products Fisher Scientific Gibco™ MEM α, Nucleosides

Get tips on using Gibco™ DMEM, high glucose to perform Stem cell Differentiation media hMSCs differentiation into myogenic cells

Products Fisher Scientific Gibco™ DMEM, high glucose

Get tips on using Gibco™ DMEM, high glucose to perform Stem cell Differentiation media hBMSCs differentiation into chondrogenic cells

Products Fisher Scientific Gibco™ DMEM, high glucose

Get tips on using QIAamp DNA Blood Mini Kit to perform DNA isolation / purification Cells - Immortalized cell lines HEK 293T

Products Qiagen QIAamp DNA Blood Mini Kit

Get tips on using DNeasy Blood and Tissue Kit (250) to perform DNA isolation / purification Cells - Immortalized cell lines Loucy

Products Qiagen DNeasy Blood and Tissue Kit (250)

Get tips on using DMEM with Glucose and L-Glutamine to perform 3D Cell Culture Media U87MG cells- glioblastoma spheres

Products Lonza DMEM with Glucose and L-Glutamine

Get tips on using Wizard® Genomic DNA Purification Kit to perform DNA isolation / purification Cells - Immortalized cell lines 3T3

Products Promega Wizard® Genomic DNA Purification Kit

Get tips on using Wizard® Genomic DNA Purification Kit to perform DNA isolation / purification Cells - Immortalized cell lines HeLa

Products Promega Wizard® Genomic DNA Purification Kit

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 Mouse Activation 3T3-L1 C/EBPβ

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