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Get tips on using Eco52I (XmaIII) restriction enzyme to perform Restriction Enzymes Eco52I / EagI

Products Takara Bio Inc Eco52I (XmaIII) restriction enzyme

Get tips on using Bsp1286I (SduI) restriction enzyme to perform Restriction Enzymes Bsp1286I / SduI

Products Takara Bio Inc Bsp1286I (SduI) restriction enzyme

Get tips on using SmiI (SwaI) restriction enzyme to perform Restriction Enzymes SwaI / SmiI

Products Takara Bio Inc SmiI (SwaI) restriction enzyme

Get tips on using BssHII (BsePI) restriction enzyme to perform Restriction Enzymes BssHII / PteI

Products Takara Bio Inc BssHII (BsePI) restriction enzyme

Get tips on using HincII (HindII) restriction enzyme to perform Restriction Enzymes HincII / HindII

Products Takara Bio Inc HincII (HindII) restriction enzyme

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 PE anti-mouse CD49b (pan-NK cells) Antibody to perform Flow cytometry Anti-bodies Mouse - CD49b

Products BioLegend PE anti-mouse CD49b (pan-NK cells) Antibody

Get tips on using E.Z.N.A.® Total RNA Kit I to perform RNA isolation / purification Cells - primary bovine umbilical vein endothelial cells

Products Omega Bio Tek E.Z.N.A.® Total RNA Kit I

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