BshNI (BanI)
Available in FastDigest® format
5'-G^G Py Pu C C-3' 3'-C C Pu Py G^G-5'
digested lambda DNA
1.0% agarose![]()
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#ER1001
Supplied with:
10X Buffer O
10X Buffer Tango™2000 u
1 ml
1 mlCommercial Isoschizomers:
AccB1I, BanI, BspT107IRelated Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER1001
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 37°C 0.3 65°C 0-20 20-50 100 50-100 0-20 100 Storage Buffer
10 mM Tris-HCl (pH 7.5 at 25°C), 200 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 BshNI, more than 95% of the digested DNA fragments can be ligated and recut.
Methylation Effects Dam:
Dcm:
CpG:
EcoKI:
EcoBI:never overlaps
may overlap
may overlap
may overlap
never overlaps- no effect.
- cleavage impaired.
- cleavage impaired.
- effect not determined.
- no effect.Compatible Ends
G^GCGCC - KasI.
G^GTACC - Acc65I, Bsp1407I, Pfl23II, TatI.Digestion of Agarose-embedded DNA
Minimum 5 units of the enzyme are required for complete digestion of 1 µg of agarose-embedded lambda DNA in 16 hours.Double Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer O NR 100 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 25 3 7 9 4 4 4 4 4 1 10
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See also General Properties of Restriction Enzymes:
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Updated balandžio 22, 2008 11:14