Test
Components | 25 to 50% Water, >50% Glycerin |
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Cut Site | C.TNAG |
Content And Storage | Keep container tightly closed |
Form | Liquid |
Storage Buffer | 10mM Tris HCl (pH 7.4 at 25°C), 100mM KCl, 1mM DTT, 1mM EDTA, 0.2mg/mL BSA, 50% Glycerol |
pH | 7.4 |
Incubator Temperature | 37°C |
Concentration | 10 U/μL |
For Use With (Application) | >95% of DNA fragments can be ligated and re-cut after 50-fold over-digesiton with DdeI |
Components | 25 to 50% Water, >50% Glycerin, 2.5 to10% Sodium Chloride |
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Cut Site | G.AATTC |
Content And Storage | Keep container tightly closed |
Form | Liquid |
Product Type | EcoRI |
Storage Buffer | 10mM Potassium Phosphate (pH 7.4 at 25°C), 300mM NaCl, 1mM EDTA, 1mM DTT, 0.2mg/mL BSA, 0.15% Triton™ X-100, 50% Glycerol |
pH | 7.4 |
Incubator Temperature | 37°C |
For Use With (Application) | >90% of DNA fragments can be ligated and re-cut after 50-fold over-digestion with EcoRI |
Components | 25 to 50% Water, >50% Glycerin |
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Cut Site | GC.GGCCGC |
Content And Storage | Keep container tightly closed |
Form | Liquid |
Product Type | NotI |
Storage Buffer | 20mM Tris HCl (pH 7.8 at 25°C), 100mM NaCl, 0.1mM EDTA, 1mM DTT, 0.02% Triton™ X-100, 0.2mg/mL BSA, 50% Glycerol |
pH | 7.4 |
Concentration | 10 U/μL |
For Use With (Application) | >90% of DNA fragments can be ligated and re-cut after 50-fold over-digestion with Not I |
Components | 25 to 50% Water, >50% Glycerin, 1 to 2.5% Potassium Chloride |
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Cut Site | A.AGCTT |
Content And Storage | Keep container tightly closed |
Format | Liquid |
Product Type | HindIII |
Storage Buffer | 10mM Tris HCl (pH 7.5 at 25°C), 250mM KCl, 1mM DTT, 0.1mM EDTA, 0.2mg/mL BSA, 50% Glycerol |
Incubator Temperature | 37°C |
Concentration | 10 U/μL |
For Use With (Application) | >95% of DNA fragments can be ligated and re-cut after 50-fold over-digestion with HaeIII |
Components | 25 to 50% Water, >50% Glycerin, 1 to 2.5% Sodium Chloride |
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Cut Site | G.GATCC |
Content And Storage | Keep container tightly closed |
Form | Liquid |
Product Type | BamHI |
Storage Buffer | 10mM Tris HCl (pH 7.4 at 25°C), 200mM NaCl, 1mM DTT, 0.1mM EDTA, 0.15% Triton™ X-100, 0.2mg/mL BSA, 50% Glycerol |
pH | 7.4 |
Incubator Temperature | 37°C |
Concentration | 10 U/μL |
For Use With (Application) | >95% of DNA fragments can be ligated and re-cut after 50-fold over-digestion with BamHI |
Components | 10X OPTIZYME™ Buffer 4 |
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Cut Site | T.CTAGA |
Form | Liquid |
Product Type | XbaI |
Storage Buffer | 10mM Tris HCl (pH 7.4), 100mM KCl, 7mM 2-mercaptoethano, 1mM EDTA, 0.2mg/mL BSA, 50% Glycerol |
pH | 7.4 |
Incubator Temperature | 37°C |
For Use With (Application) | Indicates ligation efficiency of DNA fragments generated by digestion with the Restriction Enzyme |