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Thermosensitive Phosphatase (TSP)

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Product No.: TSP01

Product Description

The phosphatase gene isolated from Antarctic psychrophilic strain TAB5 was expressed in Escherichia coli and purified for several times. Phosphatase can catalyze the removal of 5 ´ phosphate groups at the ends of DNA or RNA. After the carrier DNA is treated with thermosensitive phosphatase during cloning, its fragment lacks the 5 ´ phosphate terminal necessary for ligase, so the carrier cannot be self-connected, which can greatly reduce the background of self-connection of the carrier. The enzyme can act on the 5 ´ protruding end, concave end and flat end.


1) Remove the phosphoric acid group at the 5 ´ end of the carrier to reduce the self-connecting background;

2) Remove dNTP and pyrophosphate residues in PCR products;

3) Remove the phosphate group at the 5 ´ end of the DNA probe and prepare the optimal substrate for the 5 ´ end phosphorylation labeling;

4) Dephosphorylation of proteins.

Usage suggestions

Heat sensitive phosphatase at 1 × TSP Buffer has the optimal enzyme activity. If the reaction is to be carried out in the restricted enzyme digestion buffer, 10 must be added to the reaction system × TSP Buffer to 1 × The final concentration was incubated at 37 ℃.

Storage temperature



Thermosensitive Phosphatase(TSP) (5U/μl)40μl
10×TSP Reaction Buffer1ml

Quality Control

After several times of column purification, only clear and single target band can be seen in SDS-PAGE gel detection; There was no residual DNA of Escherichia coli and no contamination of endonuclease and exonuclease detected by PCR.

Reaction conditions

1×TSP Reaction Buffer [50 mM Bis Tris propane HCl, 1 mM MgCl2, 0.1 mM ZnCl2 (pH 6.0 at 25 ℃)], incubated at 37 ℃.

Unit definition

At 37 ℃ for 30 minutes, the amount of enzyme required to dephosphorylate 1ug pUC19 DNA Digested by Hind III (producing 5 ´ protruding end), EcoR V (producing smooth end) or Pst I (producing 5 ´ concave end) is defined as a unit.

Dephosphorylation standard refers to inhibit the reconnection of more than 95% DNA fragments in the connection reaction (detected by electrophoresis).

Thermal deactivation

70 ℃ for 5 minutes.

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