SmiI (SwaI)
Available in FastDigest® format
5'-A T T T^A A A T-3' 3'-T A A A^T T T A-5'
digested Ad2 DNA
0.7% agarose![]()
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#ER1241
Supplied with:
10X Buffer O
10X Buffer Tango™1000 u
1 ml
1 ml#ER1242
Supplied with:
10X Buffer O
10X Buffer Tango™5000 u
2x1 ml
1 mlCommercial Isoschizomers: SwaI Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER1241, #ER1242
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 O 30°C 0.1 65°C 0-20 0-20 100 20-50 0-20 20-50 Storage Buffer
10 mM Tris-HCl (pH 7.5 at 25°C), 200 mM NaCl, 1 mM DTT, 0.1 mM EDTA, 0.2 mg/ml BSA and 50% glycerol.Ligation and Recleavage
After 50-fold overdigestion with SmiI, more than 80% of the digested DNA fragments can be ligated in a reaction mixture containing 20-40 u of T4 DNA Ligase/1 µg of fragments and 10% PEG. More than 95% of these can be 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.
- effect not determined.Digestion of Agarose-embedded DNA
Minimum 10 units of the enzyme are required for complete digestion of 1 µg of agarose-embedded Adenovirus-2 DNA in 16 hours.
Note
- Assayed using Adenovirus-2 DNA.
- Incubation at 37°C results in 70% activity.
Double Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer O NR 20-50 NR: buffer is not recommended, since enzyme activity is less than 20%.
Number of Recognition Sites in DNA Molecules
Ad2 Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184 1 0 0 1 0 0 0 0 0 0 0 0
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See also General Properties of Restriction Enzymes:
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Updated balandžio 22, 2008 11:37