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Spe I (200U/vl Cat.#1055), "B" buffer
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  Store at -20¡É. For Research Use Only!

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Spe  I

Ahl I, Bcu I

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

#1055

200 units

#1055L

1,000 units

Supplied with : 10X Reaction Buffer 'B'


Concentration :            units/§¡


Lot # :                


Expiration date :                


Source : Sphaerotilus  natans  (ATCC 13923)


Compatible ends (5'¡¦CTAG)

Ahl I, AspA2 I, AsuNH I, Avr II, Bcu I, Bln I, Nhe I, Xba I, XmaJ I


Isoschizomers : Ahl I, Bcu I


Methylation Sensitivity

: Not sensitive to dam, dcm and CpG methylation


Unit definition : One Unit is defined as the amount of Spe I required to completely digest 1 §¶ of Ad-2 DNA in one hour at 37¡É in 50 §¡ assay mixture.


Typical Reaction Conditions : Add 5 §¡ of 10X Reaction Buffer 'B'[final conc.: 6 mM Tris-HCl(pH 7.5 @ 37¡É), 6 mM MgCl2, 50 mM NaCl, 1 mM DTT], 1~2 §¡ of DNA(0.5~1.0 §¶/§¡), 1 §¡ of Spe 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

Activity(%)

75~100

75~100

75~100

75~100



Activity in a complete PCR Mix : 75~100%
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 Spe 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 KCl, 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

pUC18

¥õX174

pBR322

M13mp18

SV40

0

3

0

0

0

0

0


Quality control

Overdigestion: The same band pattern as a digestion in one unit of Spe I for one hour was showing after incubation of 1 §¶ of Ad-2 DNA with         units of Spe 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 Ad-2 DNA fragments were ligated with T4 DNA ligase at 16¡É and        % of the ligated fragments could be recut with Spe I.


Notes

- Conditions of low ionic strength, high enzyme concentration, glycerol > 5%, or pH > 8.0 may result in star activity.

- Spe I cleaves to leave a 5'¡¦CTAG which can be ligated to fragments generated by Avr II, Nhe I, Sty I (C/CTAGG), and Xba I.

- Incubation of Spe I at 45¡ÆC results in an increase in activity. On the other hand, it is only 0~25% active at 25¡ÆC.


References

Roberts, R.J. Nucleic Acids Res. 13: r165-r200 (1985)


Beams Biotechnology Co., Ltd.


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