BspLI (NlaIV)
Available in FastDigest® format
5'-G G N^N C C-3' 3'-C C N^N G G-5'
digested lambda DNA
1.4% agarose![]()
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#ER1151
Supplied with:
10X Buffer Tango™200 u
1 ml#ER1152
Supplied with:
10X Buffer Tango™1000 u
1 mlCommercial Isoschizomers: BmiI, NlaIVm, PspN4I
"m" indicates different sensitivity to methylation.Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER1151, #ER1152
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 0.3 65°C 50-100 50-100 0-20 20-50 100 20-50 Storage Buffer
10 mM Tris-HCl (pH 7.4 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 BspLI, approximately 90% of the digested DNA fragments can be ligated and more than 95% of these can be recut.
Methylation Effects Dam:
Dcm:
CpG:
EcoKI:
EcoBI:never overlaps
may overlap
may overlap
never overlaps
never overlaps- no effect.
- cleavage impaired.
- cleavage impaired.
- no effect.
- no effect.Double Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer Tango™ 100 20-50 Number of Recognition Sites in DNA Molecules
Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184 82 6 18 24 11 12 13 15 15 10 23
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See also General Properties of Restriction Enzymes:
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Updated balandžio 22, 2008 11:14