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Sma I (1.5KU/vl Cat.#1053), "F" buffer
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  Store at -20¡É. For Research Use Only!

CpG   ¡Ú   25¡É

Sma  I

5' ¡¦ C C C G G G ¡¦ 3'
3' ¡¦ G G G C C C ¡¦ 5'

#1053

1,500 units

#1053L

7,500 units

Supplied with : 10X Reaction Buffer 'F'


Concentration :            units/§¡


Lot # :                


Expiration date :                


Source : Serratia marcescens (ATCC 49779)


Compatible ends : with any blunt end


Isoschizomers : CfrJ4 I, PaeB I, PspAL I

- neoschizomers : Cfr9 I, TspM I, Xma I, XmaC I


Methylation Sensitivity

: Not sensitive to dam and dcm methylation

: Blocked by CpG methylation


Unit definition : One Unit is defined as the amount of Sma I required to completely digest 1 §¶ of ¥ë DNA in one hour at 25¡É in 50 §¡ assay mixture.


Typical Reaction Conditions : Add 5 §¡ of 10X Reaction Buffer 'F'[final conc.: 10 mM Tris-HCl (pH 7.5 @ 37¡É), 7 mM MgCl2, 50 mM KCl, 1 mM DTT], 1~2 §¡ of DNA(0.5~1.0 §¶/§¡), 1 §¡ of Sma I and 42~43 §¡ of sterile water in 50 §¡ reaction mixture. Incubate at 25¡É.


Heat Inactivation : 65¡É for 20 min.


Activity in BeamsBio¢â Buffer System

Rxn Buffer

A

B

C

D

F

Activity(%)

<10

<10

<10

<10

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 Sma I. And then incubate at 25¡É for one hour. Relative activity is determined by gel electrophoresis.


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


No. of Cleavage Sites

¥ë

Ad2

pUC18

¥õX174

pBR322

M13mp18

SV40

3

12

1

0

0

1

0


Quality control

Overdigestion: The same band pattern as a digestion in one unit of Sma I for one hour was showing after incubation of 1 §¶ of ¥ë DNA with         units of Sma I for 16 hr in 50 §¡ of reaction mixture at 25¡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 Sma I.


Notes

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

- The reaction temperature for Sma I is 25¡ÆC. Incubation at 37¡ÆC gives 50% activity. Sma I has a half-life of 15 minutes at 37¡ÆC.

- Activities of Sma I in Reaction Buffer 'A', 'B', 'C' and 'D' are less than 10%, because Sma I requires potassium ion to work.

So we recommend a buffer 'F'[final conc.: 10 mM Tris-HCl (pH 7.5 @ 37¡É), 7 mM MgCl2, 50 mM KCl, 1 mM DTT].


References

Endow, S.A., Roberts, R.J. J. Mol. Biol. 112: 521-529 (1977)/ Youssoufian, H., Mulder, C. J. Mol. Biol. 150: 133-136 (1981)


Beams Biotechnology Co., Ltd.


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