PasI
A 5'-C C^C T G G G-3' 3'-G G G A C^C C-5' T
digested lambda DNA
0.7% agarose![]()
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#ER1861
Supplied with:
10X Buffer PasI200 u
1 mlCommercial Isoschizomers: - Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER1861
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, %
PasI
(unique)B
(blue)G
(green)O
(orange)R
(red)Tango™
(yellow)1X 1X 1X 1X 1X 1X 2X Buffer PasI 55°C 0.2 80°C 100 NR NR NR NR NR NR NR: buffer is not recommended, because of high star activity.
Storage Buffer
10 mM Tris-HCl (pH 7.4 at 25°C), 100 mM KCl, 1 mM DTT, 1 mM EDTA, 0.2 mg/ml BSA and 50% glycerol.Ligation and Recleavage
After 10-fold overdigestion with PasI, more than 90% of the digested DNA fragments can be ligated and recut.
Methylation Effects Dam:
Dcm:
CpG:
EcoKI:
EcoBI:never overlaps
completely overlaps
never overlaps
never overlaps
never overlaps- no effect.
- no effect.
- no effect.
- no effect.
- no effect.Digestion of Agarose-embedded DNA
Minimum 10 units of the enzyme are required for complete digestion of 1 µg of agarose-embedded lambda DNA in 16 hours.
Note
Incubation at 37°C results in 30% activity.
Greater than 10-fold overdigestion with PasI may result in star activity.
Double Digestions using Tango™ Buffer
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer PasI NR NR NR: buffer is not recommended, because of high star activity.
Number of Recognition Sites in DNA Molecules
Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184 2 0 0 0 0 0 0 0 0 0 2
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See also General Properties of Restriction Enzymes:
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Updated vasario 06, 2008 16:06