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Swa I (800U/vl Cat.#1116), Àü¿ë buffer
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  Store at -20¡É. For Research Use Only!

¡Ú  25¡É

Swa  I

Smi I

5' ¡¦ A T T T A A A T ¡¦ 3'
3' ¡¦ T A A A T T T A ¡¦ 5'

#1116

800 units

#1116L

4,000 units

Supplied with : 10X Reaction Buffer 'Swa I', 10X BSA


Concentration :            units/§¡


Lot # :                


Expiration date :                


Source : Staphylococcus  warneri


Compatible ends : with any blunt end


Isoschizomers : Smi I


Methylation Sensitivity

: Not sensitive to dcm, dam and CpG methylation


Unit definition : One Unit is defined as the amount of Swa I required to completely digest 1 §¶ of Ad-2 DNA in one hour at 25¡É in 50 §¡ assay mixture.


Typical Reaction Conditions : Add 5 §¡ of 10X Reaction Buffer 'Swa I'[final conc.: 50 mM Tris-HCl (pH 7.9 @ 25¡É), 10 mM MgCl2, 100 mM NaCl, 1 mM DTT], 1~2 §¡ of DNA(0.5~1.0 §¶/§¡), 5 §¡ of 10X BSA(final conc.: 100 §¶/§¢), 1 §¡ of Swa I and 37~38 §¡ 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

'Swa I'

Activity(%)

<10

<10

50~75

75~100

75~100


Activity in a complete PCR Mix : less than 10%
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 Swa I. And then incubate at 25¡É for one hour. Relative activity is determined by gel electrophoresis.


Storage Conditions : 10 mM Tris-HCl (pH 7.4 @ 25¡É), 400 mM NaCl, 0.1 mM EDTA, 1 mM DTT, 200 §¶/§¢ BSA, and 50% glycerol. Store at -20¡É.


No. of Cleavage Sites

¥ë

Ad2

pUC18

¥õX174

pBR322

M13mp18

SV40

0

1

0

0

0

1

1


Quality control

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


Notes

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

- Swa I is very unstable at 37¡ÆC(50% activiy). The reaction temperature for Swa I is 25¡ÆC.


References

Lechner, M., Frey, B., Laue, F., Anton-Botella, J., Smith, C.L., Ankenbauer, W., Schmitz, G.G. Nucleic Acids Res. 20: 2293-2296 (1992)


Beams Biotechnology Co., Ltd.


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