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. : EROT0368
| Cat. No. | EROT0368 |
| Recognition Site | CTN↓NAC |
| Size | 200 Units;400 Units |
| Reaction Buffer | 3mM 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 (pH7.5 at 25 °C), 50mM KCl, 1mM DTT, 0.1mM EDTA, 0.5mg/mL BSA and 50% (v/v) glycerol |
A: The specific recognition sequence of Hpy8I restriction enzyme is 5'-GTNACC-3'.
A: The cutting efficiency of Hpy8I may be affected by factors such as substrate DNA concentration, enzyme concentration, reaction time, reaction temperature, and buffer system.
A: Different buffer systems may have different impacts on Hpy8I's activity, and the optimal buffer system needs to be determined through experimentation.
A: Hpy8I may have advantages in certain applications due to its specific recognition sequence or cutting efficiency, but specific advantages need to be evaluated based on the experimental objectives and conditions.
A: The cutting product ends of Hpy8I are 3' overhangs, meaning, it produces sticky ends.
A: Hpy8I can be used in DNA cloning, genomic analysis, gene tagging, and other DNA manipulation-related molecular biology applications.
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