Taq DNA Polymerase Selection Guide
Guidelines to help you choose the right Taq formulation for your needs
Factors to consider when choosing a thermostable polymerase for your PCR include the intended application, enzyme characteristics, fidelity, reaction optimization needs and ease-of-use.
We offer a full range of high-quality Taq DNA polymerase formulations that include optimized enzymes and buffer systems for reliable, robust amplification. Taq DNA polymerase products include hot-start and standard PCR options, master mixes, and customizable buffer systems. We also offer Pfu DNA polymerase for applications requiring higher fidelity amplification.
Review the properties of the various Taq and Pfu formulations using the table below to choose the enzyme best suited to your research needs.
Manufacturing Facility India
General Applications
Multiplexing
Takara Taq DNA Polymerase
(R001A)
-Routine Use
-<12kb Lambda DNA
-TA overhang
-High Yield (RR320A)
-Hot Start (RR330A)
Low Copy Number
High Yield
Takara Ex Taq DNA Polymerase
(RR001A)
-Proof Reading
-High Yield
-Upto 30 Kb
-TA overhang
-Hot Start (RR006A)
Genotyping
EmeraldAmp GT PCR Master Mix
(RR310A)
-Upto 4kb
-TA overhang
-Dye Added
-No purification step needed
-High Yield (RR320A)
-Hot Start (RR330A)
Long PCR,
Sequencing, Cloning
Takara LA Taq DNA Polymerase
(RR002A)
-<48b Lambda DNA
-<30kb gDNA
-TA Overhang
-60 sec/ kb
-Hot Start (RR042A)
