Technical Data
T0716
TaiI (MaeII)
400U
2000U
Molecular Biology Storage: -20CShipping: Blue Ice
5'-A C G T^-3'
3'-^T G C A-5'
Tail-neoschizomer of MaeII, produces DNA fragments that have a 4-base 3-extension

Concentration:
~10u/ul

Source:
Thermus aquaticus Cc1331

Restriction Enzyme Buffer E, 10X; R1625-04, Included: 10mM Tris-HCl (pH 8.5), 10mM MgCl2, 100mM KCl and 0.1mg/ml BSA. Incubate at 65C**

Diluent Buffer:
Dilute with 10mM Tris-HCl (pH 7.4 at 25C), 100mM KCl, 1mM EDTA, 1mM DTT, 0.2mg/ml BSA and 50% glycerol.

Storage Buffer:
Supplied as a liquid in 10mM Tris-HCl (pH 7.5 at 25C), 100mM KCl, 1mM DTT, 0.1mM EDTA, 0.2mg/ml BSA and 50% glycerol.
Overdigestion Assay:
No detectable change in the specific fragmentation pattern is observed after 160-fold overdigestion (10u/ug lambda DNA x 16 hours) with TaiI.

Ligation/Recutting Assay:
After 50-fold overdigestion (3 units/ug DNA x 17 hours) with TaiI, more than 95% of the DNA fragments can be ligated at a 5'-termini concentration of 1.5uM. More than 95% of these can be recut.

Labeled Oligonucleotide (LO) Assay:
No detectable degradation of a single-stranded and double-stranded labeled oligonucleotide was observed after incubation with 10 units of restriction endonuclease for 4 hours.

Methylation Effects:
TaiI does not cut Am5CGT. Blocked by CG methylation.

Stability during Prolonged Incubation:
A minimum of 0.3 units of enzyme is required for complete digestion of 1ug of lambda DNA in 16 hours at 65C.

Thermal Inactivation:
Enzyme is not inactivated by incubation at 80C for 20min.

Compatible Ends:
AatII

Number of Recognition Sites in DNA:

Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.