YEAtaq II DNA Polymerase
Description
YEAtaq II DNA Polymerase is a thermostable enzyme derived from Thermus aquaticus YT-1 strain.
The enzyme is in a recombinant form expressed in E. coli. It is able to with stand repeated heating to 95°C without significant loss of activity.
It possesses both 5’-3’ polymerase and exonuclease activity, and has no detectable 3’-5’ exonuclease activity.
It has a 3’ adenylation activity. Thus, the PCR products can be used directly in TA-cloning procedures.
Features
• 1 kb/ 1 min
Applications
• Cloning and expression
• Mutation analysis
• Efficient & highly sensitive PCR use
• Mutation analysis
• Efficient & highly sensitive PCR use
Unit Definition
One unit is defined as the amount of enzyme that will incorporate 10 nmol of dNTPs into an acid-insoluble material in 30 minutes at 72 °C.
One unit is defined as the amount of enzyme that will incorporate 10 nmol of dNTPs into an acid-insoluble material in 30 minutes at 72 °C.
Quality Control
• Nuclease activity is not detected after incubation of 1 μg λ/Hind III DNA with 5 units of HiFi DNA polymerase in 50 μl reaction buffer for 18 hours at 37 °C.
• The absence of endo-, exodeoxyribonucleases and ribonucleases are confirmed
by appropriate tests. A functional test is performed by PCR.
• The absence of endo-, exodeoxyribonucleases and ribonucleases are confirmed
by appropriate tests. A functional test is performed by PCR.
Store at
# FYT601-500U (500 units)
YEAtaq II DNA Polymerase | 100 μl (5 U/μl) |
10× Reaction Buffer | 1 ml |
dNTPs Mix | 200 μl (10 mM) |
# FYT611-500U (500 units)
HiFi DNA Polymerase | 100 μl (5 U/μl) |
10× Reaction Buffer | 1 ml |
Storage Buffer
20 mM Tris-HCl (pH 8.0), 100 mM KCl, 0.1 mM EDTA, 0.5% Tween 20, 1 mM DTT, 50% Glycerol, Stabilizers
10× Reaction Buffer*
15 mM MgCl2, Tris-HCl (pH 8.3), (NH4)2SO4, KCl
* The reaction buffer is supplied as a 10× concentrate and should be diluted before use.
Manual |