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Content
2,500U
Applications
lPrimer labelling
lSecond strand cDNA synthesis
lDNA strand displacement synthesis
lSingle dA tailing
Thermal Inactivation
75℃, 20 min.
Unit Definition
One unit is defined as adding 10 nmol acidic refractory substance in 30 min at 37℃.
Buffer
l1X Bsu Buffer: 50 mM NaCl, 10 mM Tris-HCl (Ph7.5), 10 mM MgCl2, 1 mM DTT.
lEnzyme storage buffer: 50 mM Tris-HCl (pH 8.0), 50 mM KCl, 1 mM DTT, 20% Glycerol.
Storage
Stored at -20℃ for 2 years.
Notes
lDue to the lack of the 3’→ 5’ exonuclease activity, Bsu DNA Polymerase (Large Fragment) cannot excise 3' protruding ends and therefore not suitable for generating blunt ends.
lAt 25℃, Bsu DNA Polymerase (Large Fragment) retains 50% activity, which is twice as high as the Klenow fragment (3´→5´ exo-) at the same temperature.
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