Home  Contacts  Order  Catalog  Support
 Search  Alphabetical Index  Numerical Index
 Restriction Enzymes  Modifying Enzymes  PCR, qPCR, RT-PCR & dNTPs  Molecular Cloning  Nucleic Acid Purification
 Molecular Labeling & Detection  In vitro Transcription  Electrophoresis Products  Nucleotides  Transfection Reagents  Reagents
C A T A L O G
 

Eco52I (EagI)
Available in FastDigest® format

5'-C^G G C C G-3'
3'-G C C G G^C-5'

digested lambda DNA
0.7% agarose
       
#ER0331
Supplied with:
10X Buffer Eco52I
10X Buffer Tango™		 500 u
 
1 ml
1 ml
#ER0332
Supplied with:
10X Buffer Eco52I
10X Buffer Tango™		 2500 u
 
1 ml
1 ml
Commercial Isoschizomers:
BseX3I, BstZI, EagI, EclXI

Related Documents (in pdf, ~55 KB):

Certificate of Analysis: #ER0331, #ER0332
MSDS (English)
MSDS (English-USA)
MSDS (German)
Chart (in pdf, 721 KB)
Brochure (in pdf, 316 KB)

Concentration
10 u/µl

Conditions for 100% Activity

Recommended
buffer		 Incubation
temperature		 Units for 
overnight 
incubation,
u/µg DNA		 Thermal
inactivation,
in 20 min

Enzyme activity, %
Eco52I
(unique)		 B 
(blue)		 G 
(green)		 O 
(orange)		 R 
(red)		 Tango™ 
(yellow)
1X 1X 1X 1X 1X 1X 2X
Buffer Eco52I 37°C 0.2 65°C 100 0-20 0-20 0-20 20-50 0-20 20-50

Storage Buffer
10 mM Tris-HCl (pH 8.2 at 25°C), 500 mM NaCl, 1 mM DTT, 0.1 mM EDTA 0.2 mg/ml BSA and 50% glycerol.

Ligation and Recutting
After 50-fold overdigestion with Eco52I, more than 95% of the digested DNA fragments can be ligated and recut.

Methylation Effects
Dam:
Dcm:
CpG:
EcoKI:
EcoBI:		  never overlaps
 never overlaps
 completely overlaps
 never overlaps
 never overlaps		 - no effect.
- no effect.
- blocked.
- no effect.
- no effect.

Digestion of Agarose-embedded DNA
Minimum 5 units of the enzyme are required for complete digestion of 1 µg of agarose-embedded lambda DNA in 16 hours.

Double Digestions using Tango™ Buffer, DoubleDigest™

Optimal
buffer

Enzyme activity, %
Tango™ 
(yellow)
1X 2X
Buffer Eco52I NR 20-50

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
2 0 0 1 0 0 0 1 1 0 1

See also General Properties of Restriction Enzymes:

 

 Home  Search  Contacts  Order  Catalog  Support

Updated kovo 06, 2008 13:42