Site Directed Mutagenesis (SDM) Human Point mutation HEK293

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pCEP-4-MBP Product

Get tips on using pCEP-4-MBP to perform Protein Expression Eukaryotic cells - HEK293 BM40

Products Manuel Koch, Institute for Dental Research and Oral Musculoskele pCEP-4-MBP

Get tips on using Qubit RNA HS Assay Kit to perform RNA quantification Fuorimetric - HEK293

Products Thermo Fisher Scientific Qubit RNA HS Assay Kit

Get tips on using ApopTag® Peroxidase In Situ Apoptosis Detection Kit to perform Apoptosis assay cell type - HEK293

Products Millipore ApopTag® Peroxidase In Situ Apoptosis Detection 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 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

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 Etv2 promoter

Get tips on using NEBNext® Multiplex Small RNA Library Prep Set for Illumina® to perform RNA sequencing Human - HEK293T

Products New England BioLabs NEBNext® Multiplex Small RNA Library Prep Set for Illumina®
pVRB2B3 Product

Get tips on using pVRB2B3 to perform Protein Expression Eukaryotic cells - HEK293 hβ-defensin 2/3

Products Rong Gao, Key Laboratory of Bio-Resource and Eco-Environment, Mi pVRB2B3

Get tips on using pGEn2-GFP-ST6GalI to perform Protein Expression Eukaryotic cells - HEK293 GFP-ST6GalI

Products Adam Barb, The Roy J. Carver Department of Biochemistry, Biophys pGEn2-GFP-ST6GalI

Get tips on using pPICZ-mEGFP-hPORCN to perform Protein Expression Eukaryotic cells - HEK293 mEGFP-hPORCN

Products Anirban Banerjee, Cell Biology and Neurobiology Branch, National pPICZ-mEGFP-hPORCN

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