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Apa I (2KU/vl Cat.#1004), "A" buffer
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  Store at -20¡É. For Research Use Only!

dcm   CpG   30¡É

Apa  I

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

#1004

2,000 units

#1004L

10,000 units

Supplied with : 10X Reaction Buffer 'A'


Concentration :            units/§¡


Lot # :                


Expiration date :                


Source : Acetobacter pasteurianus NCIB 7215


Compatible ends (GGCC¡¦3') : Ppe I


Isoschizomers

: Bsp1201 I(neoschizomer), PspOM I(neoschizomer)


Methylation Sensitivity

: Not sensitive to dam methylation

: Blocked by overlapping dcm methylation

: Blocked by overlapping CpG methylation


Unit definition : One Unit is defined as the amount of Apa I required to completely digest 1 §¶ of pXba DNA in one hour at 30¡É in 50 §¡ assay mixture.


Typical Reaction Conditions : Add 5 §¡ of 10X Reaction Buffer 'A'[final conc.: 6 mM Tris-HCl (pH 7.5 @ 37¡É), 6 mM MgCl2, 6 mM NaCl, 1 mM DTT], 1~2 §¡ of DNA(0.5~1.0 §¶/§¡), 1 §¡ of Apa I and 42~43 §¡ of sterile water in 50 §¡ reaction mixture. Incubate at 30¡É.


Heat Inactivation : 65¡É for 20 min.


Activity in BeamsBio¢â Buffer System

Rxn Buffer

A

B

C

D

Activity(%)

75~100

50~75

50~75

<10


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 Apa I. And then incubate at 30¡É for one hour. Relative activity is determined by gel electrophoresis.


Storage Conditions : : 10 mM Tris-HCl(pH 7.4 @ 25¡É), 100 mM KCl, 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

pXba

pUC18

¥õX174

pBR322

M13mp18

SV40

1

5

0

0

0

0

1


Quality control

Overdigestion: The same band pattern as a digestion in one unit of Apa I for one hour was showing after incubation of 1 §¶ of DNA with         units of Apa I for 16 hr in 50 §¡ of reaction mixture at 30¡É as determined by agarose gel electrophoresis.

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


Notes

- Optimal activity is at 30~32¡ÆC. Incubation at 37¡ÆC results in 100% activity, however, the half-life of Apa I at 37¡ÆC is

only 30 minutes.

- Apa I is inhibited by salt concentrations above 50 mM.


References

Seurinck, J., Van de Voorde, A., Van Montagu, M., Nucleic Acids Res., 11: 4409-4415 (1983)/ Yamada, Y., Murakami, M., Agric. Biol. Chem., 49: 3627-3629 (1985)/ Larimer, F.W., Nucleic Acids Res., 15: 9087 (1987)


Beams Biotechnology Co., Ltd.


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