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C A T A L O G
 

Tru1I (MseI)
Available in FastDigest® format

5'-T^T A A-3'
3'-A A T^T-5' 

digested lambda DNA
1.4% agarose
      
#ER0981
Supplied with:
10X Buffer R
10X Buffer Tango™ 
300 u
 
1 ml
1 ml
#ER0982
Supplied with:
10X Buffer R
10X Buffer Tango™
1500 u
 
1 ml
1 ml
#ER0983
Supplied with:
10X Buffer R
10X Buffer Tango™
HC, 1500 u
 
1 ml
1 ml
Commercial Isoschizomers: MseI, Tru9I

Related Documents (in pdf, ~55 KB):

Certificate of Analysis: #ER0981, #ER0982, #ER0983
MSDS (English)
MSDS (English-USA)
MSDS (German)
Chart (in pdf, 721 KB)
Brochure (in pdf, 316 KB)

Concentration
10 u/µl; 50 u/µl, HC

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 65°C 0.2 No 50-100 50-100 20-50 100 50-100 100

Storage Buffer
10 mM Tris-HCl (pH 7.4 at 25°C), 100 mM KCl, 1 mM DTT, 1 mM EDTA, 0.2 mg/ml BSA and 50% glycerol.

Ligation and Recleavage
After 50-fold overdigestion with Tru1I, more than 90% of the digested DNA fragments can be ligated and recut.

Methylation Effects
Dam:
Dcm:
CpG:
EcoKI:
EcoBI:
 never overlaps
 never overlaps
 never overlaps
 may overlap
 never overlaps
- no effect.
- no effect.
- no effect.
- blocked.
- no effect.

Compatible Ends
AseI, BfaI, Csp6I, FspBI, NdeI, VspI.

Note
Incubation at 37°C results in 10% activity. We recommend using Tru1I, HC (#ER0983) at 37°C.

Double Digestions using Tango™ Buffer, DoubleDigest™

Optimal
buffer

Enzyme activity, %

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

Number of Recognition Sites in DNA Molecules

Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184
195 35 63 15 13 13 18 19 19 16 12

See also General Properties of Restriction Enzymes:

 

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Updated balandžio 22, 2008 11:36