DNA methylation profiling Gene specific profiling Rat whole pituitary glands

- Found 5696 results

siRNA / miRNA gene silencing Mouse - Glomerular mesangial cells HIPK2 Polymer / Lipid delivery Experiment

RNA siRNA / miRNA gene silencing Mouse Glomerular mesangial cells HIPK2 Polymer / Lipid delivery

siRNA / miRNA gene silencing Human - Jurkat MK2 (MAPK Kinase 2) Viral vectors Experiment

RNA siRNA / miRNA gene silencing Human Jurkat MK2 (MAPK Kinase 2) Viral vectors

siRNA / miRNA gene silencing Human - U937 MK2 (MAPK Kinase 2) Viral vectors Experiment

RNA siRNA / miRNA gene silencing Human U937 MK2 (MAPK Kinase 2) Viral vectors

DNA isolation / purification Cells - Immortalized cell lines Human Neuroblastoma Cell Lines Experiment

DNA DNA isolation / purification Cells Immortalized cell lines Human Neuroblastoma Cell Lines

siRNA / miRNA gene silencing Human - HNSCC cell line Eph receptor B4 Polymer / Lipid Experiment

RNA siRNA / miRNA gene silencing Human HNSCC cell line Eph receptor B4 Polymer / Lipid

siRNA / miRNA gene silencing Human - Primary Human Aortic Endothelial Cells GLO-1 Lipid Experiment

RNA siRNA / miRNA gene silencing Human Primary Human Aortic Endothelial Cells GLO-1 Lipid

GeneArt™ Site-Directed Mutagenesis PLUS System Product

Get tips on using GeneArt™ Site-Directed Mutagenesis PLUS System to perform Site Directed Mutagenesis (SDM) Rat - Point mutation Rat-2 PIK3CB

Products Thermo Fisher Scientific GeneArt™ Site-Directed Mutagenesis PLUS System

siRNA / miRNA gene silencing Human - 501 Mel and SK Mel 28 FANCD2 Polymer / Lipid Experiment

RNA siRNA / miRNA gene silencing Human 501 Mel and SK Mel 28 FANCD2 Polymer / Lipid

siRNA / miRNA gene silencing Human - Primary Endometrial Stromal Cells hsa-miR-542-3p Lipid Experiment

RNA siRNA / miRNA gene silencing Human Primary Endometrial Stromal Cells hsa-miR-542-3p Lipid

CRISPR Human - Repression HBV RT Experiment

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 RT

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