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. : EROT0380
| Cat. No. | EROT0380 |
| Recognition Site | GCTCTTC(1/4)↓ |
| Size | 500 Units |
| Reaction Buffer | 33mM Tris-acetate (pH 7.9 at 37 °C), 10mM Mg-acetate, 66mM K-acetate and 0.1mg/mL BSA |
| Reaction Conditions | Incubate at 37 °C |
| Storage | 10mM Tris-HCl (pH 7.4 at 25°C), 100mM KCl, 1mM DTT, 1mM EDTA, 0.2mg/mL BSA and 50% (v/v) glycerol |
A: The optimal cutting conditions for LguI can be identified by testing different ion strengths, pH values, and temperatures. Manufacturers typically provide recommended reaction conditions.
A: Incomplete digestion may be due to poor DNA quality, DNA methylation, low enzyme activity, or inappropriate reaction buffer systems.
A: The enzyme should be stored under the conditions recommended by the manufacturer and avoid repeated freeze-thaw cycles. If activity decreases, consider increasing the amount of enzyme used.
A: LguI can be used to construct recombinant vectors, but it is important to ensure that the enzyme cutting sites on the vector and the insert are matched and that the ends of the insert are compatible.
A: Self-ligation can be prevented by dephosphorylating the 5'-phosphate groups of the fragments or by using the enzyme's star activity conditions.
A: Yes, LguI recognizes and cuts specific nucleotide sequences, so it is essential to ensure that the target DNA contains the recognition sequence for LguI in the experimental design.
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