TasI (Tsp509I)
Available in FastDigest® format
5'-^A A T T -3' 3'- T T A A^-5'
digested lambda DNA
1% agarose![]()
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#ER1351
Supplied with:
10X Buffer B
10X Buffer Tango™1000 u
1 ml
1 ml#ER1352
Supplied with:
10X Buffer B
10X Buffer Tango™5000 u
2x1 ml
1 mlCommercial Isoschizomers:
Sse9I, Tsp509I, TspEIRelated Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER1351, #ER1352
MSDS (English)
MSDS (English-USA)
MSDS (German)
Chart (in pdf, 721 KB)
Brochure (in pdf, 316 KB)Concentration
10 u/µlConditions 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 B 65°C
under paraffin oil in a capped vial0.3 No 100 50-100 20-50 0-20 20-50 0-20 Storage Buffer
10 mM Tris-HCl (pH 7.5 at 25°C), 50 mM KCl, 1 mM DTT, 0.1 mM EDTA, 0.2 mg/ml BSA and 50% glycerol.Ligation and Recleavage
After 50-fold overdigestion with TasI, more than 95% of the digested DNA fragments can be ligated and recut.
Methylation Effects Dam:
Dcm:
CpG:
EcoKI:
EcoBI:never overlaps
never overlaps
never overlaps
never overlaps
may overlap- no effect.
- no effect.
- no effect.
- no effect.
- blocked.Note
Incubation at 37°C results in less than 10% activityDouble Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer B 20-50 NR NR: buffer is not recommended, since enzyme activity is less than 20%.
Number of Recognition Sites in DNA Molecules
Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184 189 25 64 8 7 7 10 12 12 14 13
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See also General Properties of Restriction Enzymes:
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Updated balandžio 22, 2008 11:36