siRNA / miRNA gene silencing Rat INS-1

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Get tips on using Mouse Rat Estradiol ELISA Kit to perform ELISA Rat - Estradiol

Products BosterBio Mouse Rat Estradiol ELISA Kit

Get tips on using Rat CX3CL1/Fractalkine DuoSet ELISA to perform ELISA Rat - CX3CL1

Products R&D Systems Rat CX3CL1/Fractalkine DuoSet ELISA

Get tips on using Rat Adiponectin ELISA Kit (ab108784) to perform ELISA Rat - Adiponectin

Products Abcam Rat Adiponectin ELISA Kit (ab108784)

Get tips on using mirVana™ miRNA Isolation Kit, with phenol to perform RNA isolation / purification Cells - immortalized PK-1

Products Thermo Fisher Scientific mirVana™ miRNA Isolation Kit, with phenol

Get tips on using mirVana™ miRNA Isolation Kit, with phenol to perform RNA isolation / purification Cells - immortalized THP-1

Products Thermo Fisher Scientific mirVana™ miRNA Isolation Kit, with phenol

Get tips on using Rat Transferrin ELISA Kit (ab137993) to perform ELISA Rat - Transferrin (Tf)

Products Abcam Rat Transferrin ELISA Kit (ab137993)

Get tips on using Rat Transferrin ELISA Kit (Colorimetric) to perform ELISA Rat - Transferrin (Tf)

Products Novus Biologicals Rat Transferrin ELISA Kit (Colorimetric)

Get tips on using Rat beta-NGF DuoSet ELISA to perform ELISA Rat - beta-NGF

Products R&D Systems Rat beta-NGF DuoSet ELISA

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 Rat Deletion PC12 Munc18

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 Rat Deletion PC12 MMP9

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