Kit of thermostable DNA polymerase, dNTPs and reaction buffer
For in vitro use only!
Unit Definition: One unit is defined as the amount of the enzyme required to catalyze the incorporation of 10 nmoles of dNTP's into an acid-insoluble form in 30 minutes at 70 °C using hering sperm DNA as substrate.
Shipping: shipped on blue ice
Storage Conditions: store at -20 °C
avoid freeze/thaw cycles
Shelf Life: 12 months
Concentration: 5 units/μl
Availability Restriction: Exclusively distributed in Japan by Greiner BioOne
Taq Core Kit contains all reagents required for PCR (except template and primer) in one box combining simple handling with high flexibility. The premium quality polymerase, ultrapure dNTPs and the optimized complete reaction buffer ensure superior amplification results. The additional reaction buffer without MgCl2 in combination with the MgCl2 stock solution allows an easy optimization of difficult amplifications.
The kit is recommended for use in routine PCR reactions. It is optimized for high specificity and guarantees minimal by-product formation. The buffer system is recommended for plate based PCR and automated pipetting.
The enzyme replicates DNA at 72 °C. It catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction in the presence of magnesium. It also possesses a 5'→3' polymerization-dependent exo-nuclease replacement activity but lacks a 3'→5' exonuclease activity.
10 mM each
|200 μl||1 ml|
|Taq Reaction Buffer complete**|
|1.2 ml||5 x 1.2 ml|
|1.5 ml||2 x 1.5 ml|
Recommended 50 μl PCR assay:
|5 μl||10x Taq Reaction Buffer complete||green cap|
|1 μl||dNTP Mix||white cap|
|1-5 μl||each Primer|
|2 - 50 ng||template DNA||-|
|0.2 - 0.5 μl|
(1 - 2.5 units)
|Taq Pol||red cap|
|Fill up to 50 μl||PCR-grade water||-|
|MgCl2 Stock Solution||1 μl||2 μl||3 μl||5 μl|
|final MgCl2 conc.||2 mM||2.5 mM||3 mM||4 mM|
|94 °C||2 min||1x|
|denaturation||94 °C||30 sec||30x|
|annealing1)||45 - 68 °C||30 sec||30x|
|elongation2)||72 °C||30 sec - 4 min||30x|
|72 °C||2 min||1x|
For optimal specificity and amplification an individual optimization of the recommended parameters may be necessary for each new template DNA and/or primer pair.