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TaiI (MaeII*)
Available in FastDigest® format

* Unlike MaeII, TaiI produces fragments with a 4-base 3'-extension


digested lambda DNA
1.4% agarose
5'- A C G T^-3'
3'-^T G C A -5' 
      
#ER1141
Supplied with:
10X Buffer R
10X Buffer Tango™
400 u
 
1 ml
1 ml
#ER1142
Supplied with:
10X Buffer R
10X Buffer Tango™
2000 u
 
1 ml
1 ml
Commercial Isoschizomers: (HpyCH4IVm), (MaeII)
"m" indicates different sensitivity to methylation.
Enzymes in parentheses have different cleavage specificities.

Related Documents (in pdf, ~55 KB):

Certificate of Analysis: #ER1141, #ER1142
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, %


(blue)

(green)

(orange)

(red)
Tango™ 
(yellow)
1X 1X 1X 1X 1X 2X
Buffer R 65°C 0.3 No 50-100 50-100 20-50 100 100 50-100

Storage Buffer
10 mM Tris-HCl (pH 7.5 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 TaiI, 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
 may overlap
 may overlap
- no effect.
- no effect.
- blocked.
- effect not determined.
- effect not determined.

Compatible Ends
AatII.

Note
Incubation at 37°C results in less than 10% activity.

Double Digestions using Tango™ Buffer, DoubleDigest™

Optimal
buffer

Enzyme activity, %

Tango™ 
(yellow)
1X 2X
Buffer R 100 50-100

Number of Recognition Sites in DNA Molecules

Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184
143 19 22 10 5 5 8 8 8 7 9

See also General Properties of Restriction Enzymes:

 

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Updated balandžio 22, 2008 11:36