CfrI (EaeI)
5'-Py^G G C C Pu-3' 3'-Pu C C G G^Py-5'
digested lambda DNA (dcm-)
1.0% agarose![]()
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#ER0161
Supplied with:
10X Buffer Tango™200 u
1 ml#ER0162
Supplied with:
10X Buffer Tango™1000 u
1 mlCommercial Isoschizomers: EaeI Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER0161, #ER0162
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 1.0 65°C 50-100* 50-100 0-20 0-20 100 0-20 * Star activity appears at a greater than 5-fold overdigestion (5 units x 1 hour).
Storage Buffer
10 mM Tris-HCl (pH 8.5 at 25°C), 500 mM KCl, 1 mM DTT, 0.1 mM EDTA, 0.5 mg/ml BSA and 50% glycerol.Ligation and Recleavage
After 50-fold overdigestion with CfrI, 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
never overlaps
never overlaps- no effect.
- blocked.
- blocked.
- no effect.
- no effect.Digestion of Agarose-embedded DNA
Note
Minimum 5 units of the enzyme are required for complete digestion of 1 µg of agarose-embedded lambda DNA in 16 hours.
Assayed using lambda DNA (dcm-) (#SD0021).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 39 2 3 6 3 3 3 4 4 4 8
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See also General Properties of Restriction Enzymes:
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Updated kovo 05, 2008 16:47