GenCrispr Cas9-N-NLS Nuclease
¥1600 | |
Z03468 | |
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¥1600 | |
Z03468 | |
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This is a basic protocol. The reagent concentrations, conditions, and parameters may need to be optimized.
1000 nM is equal to 160 ng/μL.
Storage & Stability | GenCrispr Cas9-N-NLS Nuclease is supplied with 1X storage buffer (10 mM Tris, 300 mM NaCl, 0.1 mM EDTA,1 mM DTT, 50% Glycerol PH7.4, at 25°C) and recommended to be stored at -20°C. Guaranteed stable for 18 months when properly stored. |
In vitro DNA cleavage assay with Z03468.
Reactions were set up according to recommended conditions, and cleavage products were resolved on a 1.5% agarose gel. Input DNA is linearized pUC57 plasmid DNA. The cleavage efficiency of Z03468 is comparable to competitors.
Lane 1, marker;
Lane 2-3, DNA + gRNA + IDT;
Lane 4-5, DNA + gRNA + Merck;
Lane 6-7, DNA + gRNA + Z03468;
Lane 8-9, negative control.
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In vivo gene editing efficiency assay of Z03468:
Cas9 and gRNA were transfected into THP1 cells by electroporation. Cells were lysed after 48h and analyzed by T7E1 assay. The editing efficiency of Z03468 is higher than competitors.
Lane 1, gRNA + Z03468;
Lane 2, gRNA + Merck;
Lane 3, gRNA + IDT;
Lane 4, gRNA + Thermo;
Lane 5, negative control;
Lane 6, marker.
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In vivo gene editing efficiency assay of Z03468:
Cas9 and gRNA were transfected into 293T cells by liposome. Cells were lysed after 48h and analyzed by T7E1 assay. The editing efficiency of Z03468 is comparable to competitors.
Lane 1, marker;
Lane 2, gRNA + Z03468;
Lane 3, gRNA + Merck;
Lane 4, gRNA + IDT;
Lane 5, negative control.
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