BseMI (BsrDI)
5'-G C A A T G N N^-3' 3'-C G T T A C^N N -5'
digested lambda DNA
0.7% agarose![]()
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#ER1261
Supplied with:
10X Buffer R
10X Buffer Tango™100 u
1 ml
1 ml#ER1262
Supplied with:
10X Buffer R
10X Buffer Tango™500 u
1 ml
1 mlCommercial Isoschizomers: Bse3DI, BsrDI Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER1261, #ER1262
MSDS (English)
MSDS (English-USA)
MSDS (German)
Chart (in pdf, 721 KB)
Brochure (in pdf, 316 KB)Concentration
5 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 55°C 0.3 80°C 0-20 20-50 0-20 100 50-100 50-100 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 BseMI, more than 95% of the digested DNA fragments can be ligated and approximately 80% of these can be recut.
Methylation Effects Dam:
Dcm:
CpG:
EcoKI:
EcoBI:never overlaps
never overlaps
may overlap
never overlaps
may overlap- no effect.
- no effect.
- no effect.
- no effect.
- effect not determined.Note
Incubation at 37°C results in 20% activity.Double Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer R 50-100 50-100 Number of Recognition Sites in DNA Molecules
Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184 44 4 3 2 2 2 2 2 2 3 1
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See also General Properties of Restriction Enzymes:
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Updated kovo 06, 2008 13:32