shRNA gene silencing Human Neuroblastoma cells (SH-SY5Y) Connexin 43

- Found 8820 results

Get tips on using CytoSelect™ 24-Well Wound Healing Assay to perform Wound healing assay cell type - human HUVEC

Products Cell Biolabs CytoSelect™ 24-Well Wound Healing Assay

Get tips on using LIVE/DEAD™ Fixable Blue Dead Cell Stain Kit, for UV excitation to perform Live / Dead assay mammalian cells - Spleen cells

Products Thermo Fisher Scientific LIVE/DEAD™ Fixable Blue Dead Cell Stain Kit, for UV excitation

Get tips on using EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit to perform ChIP Human - Glioblastoma cell line

Products Merck Millipore EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit

Get tips on using SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003 to perform ChIP Human - Glioblastoma cell line

Products Cell Signaling Technology SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003

Get tips on using EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit to perform ChIP Human - Fibroblast cell lines

Products Merck Millipore EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit

Get tips on using TRIzol Reagent to perform RNA isolation / purification Cells - immortalized SHG44

Products Thermo Fisher Scientific TRIzol Reagent

Get tips on using GenJet™ In Vitro DNA Transfection Reagent to perform DNA transfection Mammalian cells - Immortalized cell lines COS7

Products SignaGen Laboratories GenJet™ In Vitro DNA Transfection Reagent

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 3T3-L1 fmnl 2/3

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 INS-1 832/13 Ep300

Get tips on using GenJet™ In Vitro DNA Transfection Reagent to perform DNA transfection Mammalian cells - Immortalized cell lines MCF-7

Products SignaGen Laboratories GenJet™ In Vitro DNA Transfection Reagent

Outsource your experiment

Fill out your contact details and receive price quotes in your Inbox

  Outsource experiment
Become shareholder Discussions About us Contact Privacy Terms