Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : EROT0458
| Cat. No. | EROT0458 |
| Recognition Site | GC↓NGC |
| Size | 200 Units |
| Reaction Buffer | 10mM Tris-HCl (pH7.5 at 37 °C), 10mM MgCl2, 50mM NaCl and 0.1mg/mL BSA |
| Reaction Conditions | Incubate at 37 °C |
| Storage | 10mM Tris-HCl (pH7.4 at 25°C), 100mM KCl, 1mM DTT, 1mM EDTA, 0.2mg/mL BSA and 50% (v/v) glycerol |
A: SatI is sensitive to CpG methylation, insensitive to Dam methylation, and insensitive to Dcm methylation.
A: When using SatI for restriction digestion, there are 380 cutting sites.
A: SatI enzyme belongs to the high-end enzymes of fast restriction endonucleases and exhibits 100% activity in both universal FastDigest buffer and FastDigest Green reaction buffer.
A: SatI enzyme is sensitive to thermal inactivation.
A: The optimal reaction temperature for SatI enzyme is 37°C.
A: SatI enzyme should be stored at -20°C.
A: The main reasons for the failure of DNA digestion reactions include the presence of inhibitory agents in the template DNA, such as phenol, chloroform, detergents, ethanol, excessive salt, EDTA, etc.
A: To remove enzymes without using phenol/chloroform, we recommend using silica column purification.
A: For convenience, both traditional restriction enzyme buffers and FastDigest universal buffers contain BSA. This eliminates the need to add BSA in a separate step.
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