DNA modification enzymesProveedor: Cytiva
E70092ZEA 201 EURE70092Z E70092Y E70092X
DNA modification enzymes
A high specific activity, heat-labile alkaline phosphatase. Completely and irreversibly inactivated in Tris buffers at pH 8,0 to 8,5 by heating for 15 minutes at 65 °C. No further treatment is necessary.
- Bacterial alkaline phosphatase recombinantly expressed in E coli
- Active in PCR and restriction endonuclease buffers
- Inactivated by heating at 75°C for 5 minutes
- Easily soluble in cold water and hot water
- Sourced from arctic shrimp (Pandalus borealis)
Use together with illustra Exonuclease I for cleaning up PCR reactions prior to downstream application such as DNA sequencing. Dephosphorylation of a restriction enzyme digested plasmid (5-20 pmol of 5'-ends, 0.1-0.5 units/pmol 5'-ends). Reduces re-ligation to < 0.5% compared to the untreated control.
One unit is the amount of the enzyme required to dephosphorylate 1 µg of linearized pUC57 DNA termini in 10 minutes at 37°C. The enzyme is purified to apparent homogeneity and is free of all contaminating endonucleases, exonucleases and ribonucleases
Unit Definition: One unit is the amount of the enzyme required to dephosphorylate 1 Â µg of linearized pUC57 DNA termini in 10 minutes at 37 °C.
Información de suministro: Includes 10X reaction buffer: 200 mM Tris-HCl, pH 8,0, 100 mM MgCl₂; dilution buffer: 50 mM Tris-HCl, pH 8,0.
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