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Pst I (10KU/vl Cat.#1042), Àü¿ë buffer
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  Store at -20¡É. For Research Use Only!

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Pst I

BspMA I

5' ¡¦ C T G C A G ¡¦ 3'
3' ¡¦ G A C G T C ¡¦ 5'

#1042

10,000 units

#1042L

50,000 units

Supplied with : 10X Reaction Buffer 'Pst I


Concentration :            units/§¡


Lot # :                


Expiration date :                


Source : Providencia  stuartii  164 (ATCC 49762)


Compatible ends (TGCA¡¦3')

BspMA I, EcoT22 I, Mph1103 I, Nsi I, Sbf I, Sda I, Sse8387 I, Zsp2 I


Isoschizomers : BspMA I


Methylation Sensitivity

: Not sensitive to dam, dcm and CpG methylation


Unit definition : One Unit is defined as the amount of Pst I required to completely digest 1 §¶ of ¥ë DNA in one hour at 37¡É in 50 §¡ assay mixture.


Typical Reaction Conditions : Add 5 §¡ of 10X Reaction Buffer 'Pst I'[final conc.: 90 mM Tris-HCl(pH 7.5 @ 37¡É), 10 mM MgCl2, 50 mM NaCl], 1~2 §¡ of DNA(0.5~1.0 §¶/§¡), 1 §¡ of Pst I and 42~43 §¡ of sterile water in 50 §¡ reaction mixture. Incubate at 37¡É.


Heat Inactivation : 65¡É for 20 min.


Activity in BeamsBio¢â Buffer System

Rxn Buffer

A

B

C

D

'Pst I'

Activity(%)

10~50

50~75

50~75

50~75

75~100



Activity in a complete PCR Mix : 50~75%
Conditions: [10 mM Tris-HCl(pH 8.3 @ 25 ¡É), 50 mM KCl, 1.5 mM MgCl2, 2 pmol of primers, 200 ¥ìM dNTP Mix, 2.5 U Taq DNA polymerase and 1 §¶ of DNA(template or substrate) in 50 §¡ of reaction volume] After 30 amplication cycles, add 5 units of Pst I. And then incubate at 37¡É for one hour. Relative activity is determined by gel electrophoresis.


Storage Conditions : 10 mM Tris-HCl (pH 7.5 @ 25¡É), 100 mM NaCl, 0.1 mM EDTA, 1 mM DTT, 0.15% Triton¢â X-100, 100 §¶/§¢ BSA, and 50% glycerol. Store at -20¡É.


No. of Cleavage Sites

¥ë

Ad2

pUC19

¥õX174

pBR322

M13mp18

SV40

28

30

1

1

1

1

2


Quality control

Overdigestion: The same band pattern as a digestion in one unit of Pst I for one hour was showing after incubation of 1 §¶ of ¥ë DNA with         units of Pst I for 16 hr in 50 §¡ of reaction mixture at 37¡É as determined by agarose gel electrophoresis.

Ligation-Recut: After a 10-fold digestion for one hour,        % of ¥ë DNA fragments were ligated with T4 DNA ligase at 16¡É and        % of the ligated fragments could be recut with Pst I.


Notes

- Conditions of high pH, low salt, high glycerol(>12%), 8% DMSO can cause star activity.

- 0.5~2 mM spermidine inhibits digestion by Pst I. Spermidine suppresses star activity of Pst I.

- The presence of adjacent runs of G-C base pairs confers significant resistance to cleavage.

- 100% dUTP incoporation reduces Pst I cleavage to 25%.


References

Smith, D.I. et al Nucleic Acids Res. 3: 343-353 (1976)/ Malyguine, E. et al Gene 8: 163-177 (1980)/ Armstrong, K., Bauer, W.R. Nucleic Acids Res. 10: 993-1007 (1982)/ Pingoud, A. Eur. J. Biochem. 147: 105-109 (1985)/ Kuosmanen, M., Poso, H. FEBS Lett. 179: 17-20 (1985)/ Glenn, T.C. et al Biotechniques 17: 1086-1090 (1994)


Beams Biotechnology Co., Ltd.


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