BcnI (NciI)
Available in FastDigest® format
G 5'-C C^C G G-3' 3'-G G G^C C-5' C
digested lambda DNA
1.4% agarose![]()
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#ER0061
Supplied with:
10X Buffer Tango™1000 u
1 ml#ER0062
Supplied with:
10X Buffer Tango™5000 u
2x1 mlCommercial Isoschizomers: AsuC2I, BpuMI, NciI Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER0061, #ER0062
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 20-50 50-100 50-100 50-100 100 50-100 Storage Buffer
10 mM potassium phosphate (pH 7.4 at 25°C), 200 mM NaCl, 1 mM EDTA, 7 mM 2-mercaptoethanol, 0.2 mg/ml BSA and 50% glycerol.Ligation and Recleavage
After 10-fold overdigestion with BcnI, more than 80% of the digested DNA fragments can be ligated in the 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
completely overlaps
never overlaps
never overlaps- no effect.
- no effect.
- cleavage impaired.
- no effect.
- no effect.Compatible Ends
Bme1390I, Fnu4HI, SatI, ScrFI.Double Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer Tango™ 100 50-100 Number of Recognition Sites in DNA Molecules
Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184 114 1 4 10 7 7 5 6 6 6 10
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See also General Properties of Restriction Enzymes:
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Updated balandžio 22, 2008 11:17