XceI (NspI)
Available in FastDigest® format
5'-Pu C A T G^Py-3' 3'-Py^G T A C Pu-5'
digested lambda DNA
0.7% agarose![]()
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#ER1471
Supplied with:
10X Buffer Tango™500 u
1 ml#ER1472
Supplied with:
10X Buffer Tango™2500 u
1 mlCommercial Isoschizomers: BstNSI, NspI Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER1471, #ER1472
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 Tango™ 37°C 0.2 65°C 50-100 0-20 0-20 0-20 100 0-20 Storage Buffer
10 mM Tris-HCl (pH 7.5 at 25°C), 300 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 XceI, more than 95% of the digested DNA fragments can be ligated and recut.
Methylation Effects Dam:
Dcm:
CpG:
EcoKI:
EcoBI:never overlaps
never overlaps
may overlap
never overlaps
never overlaps- no effect.
- no effect.
- no effect.
- no effect.
- no effect.Double Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer Tango™ 100 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 32 0 6 4 3 3 2 1 1 1 2
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See also General Properties of Restriction Enzymes:
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Updated balandžio 22, 2008 11:34