| Compatible Buffer | 10X Buffer R |
|---|---|
| Product Type | Restriction Enzyme |
| Quantity | 4,000 units |
| Concentration | 10 U/μL |
| Enzyme | Eco47I (AvaII) |
| Methylation Sensitivity | CpG Methylation-Sensitive |
| Optimal Reaction Temperature | 37°C |
| Research Category | Traditional Cloning |
| Sensitive to Heat Inactivation | Yes |
| Type IIS RE | No |
| Unit Size | Each |
Answer:It recognizes the sequence GGWCC, where W can be A or T.
Answer:The enzyme is supplied at 10 U/µL with 4000 total units.
Answer:The enzyme performs optimally at 37 °C in a compatible restriction-enzyme buffer.
Eco47I (AvaII) is a type II restriction endonuclease used for sequence-specific cleavage of double-stranded DNA. The enzyme recognizes the degenerate sequence GGWCC, where W represents A or T, and cleaves within the recognition site to generate defined DNA fragments. This configuration provides 4000 units at a concentration of 10 U/µL. Optimal digestion is performed at 37 °C using a compatible restriction-enzyme buffer. Eco47I is an isoschizomer of AvaII and can be incorporated into cloning, restriction mapping, DNA construct verification and other workflows that require cleavage at GGWCC sites. Reaction design should account for the number of recognition sites, DNA quantity, buffer compatibility and any additional enzymes used in a double-digestion workflow. Complete digestion should be confirmed when fragment integrity is critical to downstream cloning or analytical interpretation. As with other restriction enzymes, methylation status and neighboring sequence context can affect practical digestion behavior and should be considered during assay design.
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