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MvaI (BstNI)
Available in FastDigest® format

       T
5'-C C^A G G-3'
3'-G G T^C C-5'
       A 

digested lambda DNA
1.4% agarose
      
#ER0551
Supplied with:
10X Buffer R
10X Buffer Tango™
2000 u
 
1 ml
1 ml
#ER0552
Supplied with:
10X Buffer R
10X Buffer Tango™
5x2000 u
 
2x1 ml
1 ml
Commercial Isoschizomers:
(AjnI), BptI, BseBI, Bst2UI, BstNI, BstOI, (EcoRIIm), (Psp6I), (PspGIm)
Enzymes in parentheses have different cleavage specificities.
"m" indicates different sensitivity to methylation.

Related Documents (in pdf, ~55 KB):

Certificate of Analysis: #ER0551, #ER0552
MSDS (English)
MSDS (English-USA)
MSDS (German)
Chart (in pdf, 721 KB)
rochure (in pdf, 316 KB)

Concentration
10 u/µl

Conditions for 100% Activity

Recommended
buffer
Incubation
temperature
Units for 
overnight 
incubation,
u/µg DNA
Thermal
inactivation,
in 20 min

Enzyme activity, %


(blue)

(green)

(orange)

(red)
Tango™ 
(yellow)
1X 1X 1X 1X 1X 2X
Buffer R 37°C 0.1 80°C(10 u) 20-50 20-50 50-100 100 20-50* 100

80°C(10 u) indicates that only small amounts of enzyme (up to 10 units) can be inactivated at 80°C in 20 minutes.
*
Star activity appears at a greater than 5-fold overdigestion (5 units x 1 hour).

Storage Buffer
10 mM Tris-HCl (pH 7.5 at 25°C), 400 mM KCl, 1 mM DTT, 0.1 mM EDTA, 0.2 mg/ml BSA and 50% glycerol.

Ligation and Recleavage
After 10-fold overdigestion with MvaI, more than 90% of the digested DNA fragments can be ligated in the reaction mixture containing 20-40 u of T4 DNA Ligase/1 µg of fragments and 10% PEG. More than 90% of these can be recut.

Methylation Effects
Dam:
Dcm:
CpG:
EcoKI:
EcoBI:
 never overlaps
 completely overlaps
 never overlaps
 never overlaps
 never overlaps
- no effect.
- no effect.
- no effect.
- no effect.
- no effect.

Compatible Ends
Bme1309I, Fnu4HI, SatI, ScrFI.

Note

Double Digestions using Tango™ Buffer, DoubleDigest™

Optimal
buffer

Enzyme activity, %

Tango™ 
(yellow)
1X 2X
Buffer R 20-50* 100

* Star activity appears at a greater than 5-fold overdigestion (5 units x 1 hour).

Number of Recognition Sites in DNA Molecules

Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184
70 2 7 6 5 5 5 5 5 8 12

See also General Properties of Restriction Enzymes:

 

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Updated balandžio 22, 2008 11:27