Tru1I (MseI)
Available in FastDigest® format
5'-T^T A A-3' 3'-A A T^T-5'
digested lambda DNA
1.4% agarose![]()
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#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 mlCommercial 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, HCConditions for 100% Activity
Recommended
bufferIncubation
temperatureUnits for
overnight
incubation,
u/µg DNAThermal
inactivation,
in 20 minEnzyme activity, %
B
(blue)G
(green)O
(orange)R
(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
bufferEnzyme 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
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See also General Properties of Restriction Enzymes:
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Updated balandžio 22, 2008 11:36