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Set I
| Enzyme name | Set I | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Prototype | SetI | ||||||||||||
| SKU | SE-E537 | ||||||||||||
| Turbo version | Not available | ||||||||||||
| High-concentration version | Available | ||||||||||||
| Recognition site | 5'… ASST▼ …3'
3'… ▲TSSA …5'
|
||||||||||||
| Source | An E.coli strain that carries the cloned Set I gene from Streptomyces werraensis 37 | ||||||||||||
| Optimal buffer | SE-buffer Y | ||||||||||||
| Optimal temperature | 55 °C | ||||||||||||
| Inactivation temperature | 80 °C | ||||||||||||
| Buffer activity |
|
||||||||||||
| Unit definition | One unit is defined as the amount of enzyme required to cleave 1 pmol of the double-stranded oligonucleotide of the below indicated structure in 1 hour at 55°C in a total reaction volume of 20 μl. | ||||||||||||
| Assayed on | Double-stranded oligonucleotide 5`-CGAGTTTAT AGCT GGGCCCAAC-3` 3`-GCTCAAATA TCGA CCCGGGTTG-5` |
||||||||||||
| Storage conditions | 10 mM Tris-HCl (pH 7.6); 100 mM NaCl; 0.1 mM EDTA; 1 mM DTT; 50% glycerol; Store at -20°C. | ||||||||||||
| Ligation | After 5-fold overdigestion with enzyme, approximately 50% of the pBR322 DNA fragments can be ligated with T4 DNA Ligase and recut. | ||||||||||||
| Nonspecific hydrolysis | |||||||||||||
| Methylation sensitivity | not tested | ||||||||||||
| Supplied with enzyme | 10 X SE-buffer Y [[HDR:Non-specific hydrolisis]]: | ||||||||||||
| Notes | Attention. SetI cleaves the canonical site as well as several additional sites with lower efficiency. Prolonged incubation may result in digestion of DNA to short oligonucleotides. | ||||||||||||
| References |
|
Set I
| Enzyme name | Set I | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Prototype | SetI | ||||||||||||
| SKU | SE-E537 | ||||||||||||
| Turbo version | Not available | ||||||||||||
| High-concentration version | Available | ||||||||||||
| Recognition site | 5'… ASST▼ …3'
3'… ▲TSSA …5'
|
||||||||||||
| Source | An E.coli strain that carries the cloned Set I gene from Streptomyces werraensis 37 | ||||||||||||
| Optimal buffer | SE-buffer Y | ||||||||||||
| Optimal temperature | 55 °C | ||||||||||||
| Inactivation temperature | 80 °C | ||||||||||||
| Buffer activity |
|
||||||||||||
| Unit definition | One unit is defined as the amount of enzyme required to cleave 1 pmol of the double-stranded oligonucleotide of the below indicated structure in 1 hour at 55°C in a total reaction volume of 20 μl. | ||||||||||||
| Assayed on | Double-stranded oligonucleotide 5`-CGAGTTTAT AGCT GGGCCCAAC-3` 3`-GCTCAAATA TCGA CCCGGGTTG-5` |
||||||||||||
| Storage conditions | 10 mM Tris-HCl (pH 7.6); 100 mM NaCl; 0.1 mM EDTA; 1 mM DTT; 50% glycerol; Store at -20°C. | ||||||||||||
| Ligation | After 5-fold overdigestion with enzyme, approximately 50% of the pBR322 DNA fragments can be ligated with T4 DNA Ligase and recut. | ||||||||||||
| Nonspecific hydrolysis | |||||||||||||
| Methylation sensitivity | not tested | ||||||||||||
| Supplied with enzyme | 10 X SE-buffer Y [[HDR:Non-specific hydrolisis]]: | ||||||||||||
| Notes | Attention. SetI cleaves the canonical site as well as several additional sites with lower efficiency. Prolonged incubation may result in digestion of DNA to short oligonucleotides. | ||||||||||||
| References |
|