TaiI (MaeII*)
Available in FastDigest® format
* Unlike MaeII, TaiI produces fragments with a 4-base 3'-extension
digested lambda DNA
1.4% agarose 5'- A C G T^-3' 3'-^T G C A -5'![]()
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#ER1141
Supplied with:
10X Buffer R
10X Buffer Tango™400 u
1 ml
1 ml#ER1142
Supplied with:
10X Buffer R
10X Buffer Tango™2000 u
1 ml
1 mlCommercial Isoschizomers: (HpyCH4IVm), (MaeII)
"m" indicates different sensitivity to methylation.
Enzymes in parentheses have different cleavage specificities.Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER1141, #ER1142
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 R 65°C 0.3 No 50-100 50-100 20-50 100 100 50-100 Storage Buffer
10 mM Tris-HCl (pH 7.5 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 TaiI, more than 95% of the digested DNA fragments can be ligated and recut.
Methylation Effects Dam:
Dcm:
CpG:
EcoKI:
EcoBI:never overlaps
never overlaps
completely overlaps
may overlap
may overlap- no effect.
- no effect.
- blocked.
- effect not determined.
- effect not determined.Compatible Ends
AatII.Note
Incubation at 37°C results in less than 10% activity.Double Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer R 100 50-100 Number of Recognition Sites in DNA Molecules
Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184 143 19 22 10 5 5 8 8 8 7 9
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See also General Properties of Restriction Enzymes:
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Updated balandžio 22, 2008 11:36