Taq DNA Polymerase Seperated Mg2+ – (4992763)

Description
Taq DNA Polymerase is a recombinant protein with a molecular weight of 94 kDa, which has been induced and expressed from Escherichia coli cloned with Thermo aquatica DNA Polymerase gene, and then purified and separated by three steps of column purification. The enzyme has good stability and strong specificity, with no exogenous nuclease and bacterial DNA pollution, and is suitable for routine PCR amplification.

One-tube Taq MasterMix (National High-Tech Product Certification)

■ The Taq MasterMix has improved specificity and sensitivity of PCR reaction and can amplify complex templates with high GC content, secondary structure and the like. As low as 2 copies of the target template can be amplified, ensuring more accurate experimental results.

■ The unique Taq MasterMix formula makes the whole reaction system very stable, and the activity will not be affected by repeated freeze-thaw or long-term storage at 4°C.

■ The stable and efficient pre-prepared PCR mixed solution can make the operation fast and simple, greatly reducing labor intensity and sampling error. High-performance PCR enhancer and optimizer are also included in the mix, which reduces the requirements on PCR conditions.

■ This product has both dye-containing and dye-free systems. Dye-containing MasterMix products can be directly electrophoresed after PCR, without loading buffer.

Two-component simple PCR reaction system (Golden PCR System)

■ The polymerase in the system has stable performance by special treatment. It can be stored for a long time at 4°C and still maintains excellent and efficient amplification effect.

■ The system comprises: Component I: Thermostable polymerase; Component II: Premixed solution of essential components for PCR reaction.

■ Simple and fast procedure: Simply mix the two components in proportion and then add with templates and primers, thus eliminating the trouble of adding various PCR reaction components one by one and saving hands-on time.

■ Accurate and efficient amplification efficiency, suitable for various conventional PCR reactions, amplification of complex templates such as templates with high GC content (> 60%), secondary structures, and large-scale gene detection.

■ The reaction system contains dyes, so that there’s no time interval between PCR and electrophoresis steps and the whole process is fast and labor-saving.