siRNA / miRNA gene silencing Human UCC (urothelial cancer cell lines)

- Found 8759 results

Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - mouse bone tissue

Products Qiagen miRNeasy Mini kit

Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - mouse liver tissue

Products Qiagen miRNeasy Mini kit

Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Tissue - mouse muscle tissue

Products Qiagen miRNeasy Mini kit

Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Bacteria - Gram positive Listeria monocytogens

Products Qiagen miRNeasy Mini kit

Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Bacteria - Gram negative Bordetella pertussis

Products Qiagen miRNeasy Mini kit

Get tips on using miRNeasy FFPE Kit to perform RNA isolation / purification Tissue - rat heart muscle tissue

Products Qiagen miRNeasy FFPE Kit

Get tips on using Click-iT™ EdU Alexa Fluor™ 555 Imaging Kit to perform Cell cytotoxicity / Proliferation assay cell type - PC-3

Products Thermo Fisher Scientific Click-iT™ EdU Alexa Fluor™ 555 Imaging Kit

Get tips on using Viability/Cytotoxicity Assay Kit for Animal Live & Dead Cells to perform Live / Dead assay mammalian cells - FE002-SK2 human skin progenitor cells

Products Biotium Viability/Cytotoxicity Assay Kit for Animal Live & Dead Cells

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 Deletion ES (embryonic stem) cells MIR

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 Deletion ES (embryonic stem) cells Slx2

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