| 5'-C A G N N N^C T G-3' |
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| 3'-G T C^N N N G A C-5' |
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| Catalog # | C0112 |
| Concentration | 10u/ul |
| Source | Comamonas acidovorans Lti 19–021 |
| Buffer | 33mM Tris-acetate (pH 7.9), 10mM magnesium acetate, 66mM potassium acetate and 0.1mg/ml BSA. Incubate at 37°C. |
| Diluent Buffer | 10mM Tris-HCl (pH 7.4 at 25°C), 100mM KCl, 1mM EDTA, 1mM DTT, 0.2mg/ml BSA and 50% glycerol. |
| Storage Buffer | 10mM Tris-HCl (pH 7.4 at 25°C), 100mM KCl, 1mM DTT, 1mM EDTA, 0.2mg/ml BSA and 50% glycerol. |
| Overdigestion Assay | No detectable change in the specific fragmentation pattern is observed after 320-fold overdigestion (20u/ug lambda DNA x 16 hours) with CaiI. |
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| Ligation/Recutting Assay | After 50-fold overdigestion (3u/ug DNA x 17 hours) with CaiI, more than 95% of the DNA fragments can be ligated at a 5'-termini concentration of 0.3uM. More than 95% of these can be recut. |
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| Labeled Oligonucleotide (LO) Assay | No detectable degradation of a single-stranded and double-stranded labeled oligonucleotide was observed after incubation with 10units of restriction endonuclease for 4 hours. |
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| Methylation Effects | CaiI does not cut CAGNNCm5CTG. Blocked by overlapping Dcm methylation. |
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| Stability during Prolonged Incubation | A minimum of 0.2units of enzyme is required for complete digestion of 1ug of lambda DNA in 16 hours at 37°C. |
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| Thermal Inactivation | Enzyme is inactivated by incubation at 65°C for 20min. |
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| Digestion of Agarose-embedded DNA | A minimum of 5units of enzyme is required for digestion of 1ug of agarose-embedded lambda DNA in 16 hours. |
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| Number of Recognition Sites in DNA | |
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| Lambda | 41 |
| PhiX174 | 0 |
| M13mp18/19 | 1 |
| pBR322 | 1 |
| pUC18/19 | 1 |
| pUC57 | 1 |
| pTZ19R/U | 1 |
| pBluescriptIIKS(-/+) | 1 |
| pBluescriptIISK(-/+) | 1 |
| pACYC177 | 1 |
| pACYC184 | 3 |
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| Unit Definition | One unit is defined as the amount of enzyme required to digest 1ug of lambda DNA in 1 hour at 37°C in 50ul of assay buffer. |