Site Directed Mutagenesis (SDM) Human Point mutation HEK293

- Found 6043 results

pcDNA-oGP1 Product

Get tips on using pcDNA-oGP1 to perform Protein Expression Eukaryotic cells - HEK293 GP1

Products Peter D. Sun, Structural Immunology Section, Laboratory of Immun pcDNA-oGP1
pMT3-RhoGC Product

Get tips on using pMT3-RhoGC to perform Protein Expression Eukaryotic cells - HEK293 RhoGC

Products Daniel D. Oprian, Dept. of Biochemistry, Brandeis University pMT3-RhoGC
pONE-40A Product

Get tips on using pONE-40A to perform Protein Expression Eukaryotic cells - HEK293 MBP

Products László Beinrohr, Institute of Enzymology, Research Centre for pONE-40A

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 Activation Neuro-2a Sim1

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 C2C12 Sgms2

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 C2C12 Sgms1
pIL-15 Product

Get tips on using pIL-15 to perform Protein Expression Eukaryotic cells - HEK293 IL-15

Products JianweiZhu, Engineering Research Center of Cell & Therapeutic An pIL-15

Get tips on using pFastBac1-TEV-TRPV1 to perform Protein Expression Eukaryotic cells - HEK293 TRPV1

Products Yifan Cheng, Department of Biochemistry and Biophysics, Keck Adv pFastBac1-TEV-TRPV1

Get tips on using pCMV-HA2/DKK1 to perform Protein Expression Eukaryotic cells - HEK293 DKK1

Products G.Y. Bao, Department of Clinical Laboratory, Yangzhou First Peop pCMV-HA2/DKK1

Get tips on using pgMAX system-DsRed2 to perform Protein Expression Eukaryotic cells - HEK293 DsRed2

Products Manabu Murakami, Department of Pharmacology, Hirosaki University pgMAX system-DsRed2

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