RseI (MslI)
Available in FastDigest® format
5'-C A Y N N^N N R T G-3' 3'-G T R N N^N N Y A C-5'
digested lambda DNA
1.2% agarose![]()
![]()
![]()
![]()
![]()
![]()
#ER2001
Supplied with:
10X Buffer R
10X Buffer Tango™200 u
1 ml
1 ml#ER2002
Supplied with:
10X Buffer R
10X Buffer Tango™1000 u
1 ml
1 mlCommercial Isoschizomers: SmiMI Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER2001, #ER2002
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 R 37°C 0.5 65°C 0-20 50-100 50-100 100 20-50 100 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 50-fold overdigestion with RseI, more than 95% of the digested DNA fragments can be ligated. More than 95% of these can be recut.
Methylation Effects Dam:
Dcm:
CpG:
EcoKI:
EcoBI:never overlaps
never overlaps
may overlap
may overlap
may overlap- no effect.
- no effect.
- no effect.
- blocked.
- effect not determined.Double Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer R 20-50 100 Number of Recognition Sites in DNA Molecules
Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184 62 7 3 7 3 3 3 4 4 4 4
|
See also General Properties of Restriction Enzymes:
|
| Home | Search | Contacts | Order | Catalog | Support |
Updated balandžio 22, 2008 11:39