Radiant™ Taq DNA Polymerase
- Short Description: Radiant™ Taq DNA Polymerase, 5u/µl, 500 / 2,500/ 10,000 units w/ separate tube 10X PCR buffer and MgCl2 High-yields with amplicons up to 5 Kb with standard or fast cycling. New-generation PCR buffer formulation including enhancers for maximum PCR efficiency and reaction speed. Robust PCR performance across a wide range of DNA templates including genomic DNA and GC-rich and AT-rich sequences. Supplied with 10X Reaction Buffer and separate MgCl2 for flexibility and optimization.
Radiant™ Taq DNA Polymerase Description RadiantTM Taq DNA Polymerase is a highly purified, high performance DNA Polymerase optimized for the sensitive DNA amplification of a wide range of DNA templates including complex mammalian genomic DNA. RadiantTM Taq DNA Polymerase exhibits 5´-3´ DNA polymerase activity with an error-rate of wild-type Taq ( 2.0 x 10-5). The polymerase is ideal for screening, colony PCR, high-throughput PCR and genotyping of problematic GC-rich and AT-rich sequences. RadiantTM Taq DNA Polymerase is engineered for robust, superior PCR and is supplied with a highly optimized, new-generation buffer system which provides exceptional sensitivity. Storage RadiantTM Taq DNA Polymerase is shipped on blue or dry ice and should be stored at –20°C upon receipt. Excessive freeze/thawing should be avoided. When stored as specified, RadiantTM Taq DNA Polymerase is stable for 12 months from date of receipt. The Kit may also be stored at 4°C for 1 month. Important Considerations RadiantTM 10x Taq Reaction Buffer: The 10x Taq reaction buffer contains proprietary PCR enhancers and has been optimized for maximum efficiency, sensitivity and success with difficult amplicons. We do not suggest the use of additional PCR enhancers. Template: For complex genomic DNA, we suggest the use of 5ng - 500ng per reaction; For cDNA or plasmid DNA, please use < 100ng per reaction. Primers: Primers should have a predicted melting temperature of around 60°C, using default Primer 3 settings (http://frodo.wi.mit.edu/primer3/). The final primer concentration in the reaction should be between 0.2μM and 0.6μM. Annealing: We recommend performing a temperature gradient to determine the optimal annealing temperature. Alternatively, we suggest a 55°C annealing temperature. Increase in 2°C increments if non-specific products are present. Extension: Optimal extension is achieved at 72°C. The optimal extension time is dependent on amplicon length and complexity. 15 seconds per kilobase(Kb) is recommended for amplification from eukaryotic genomic DNA or cDNA. For shorter amplicons, a 1 second extension is sufficient. Quality Control RadiantTM Taq DNA Polymerase is tested extensively for robust activity, processivity, efficiency, heat activation, sensitivity, absence of nuclease contamination and absence of nucleic acid contamination. RadiantTM Taq DNA Polymerase is manufactured under a comprehensive quality management system, following ISO 9001:2008 standards. Limitations of Use This product is intended for research purposes only and is not intended for any animal or human therapeutic use. Technical Support For Trouble-shooting and Technical Guidance, please contact us at firstname.lastname@example.org and provide PCR reaction conditions, cycling parameters, amplicon size, and screen grabs (gel images) if possible. Alkali Scientific guarantees the performance of all products in the manner described in our product literature. The purchaser must determine the suitability of the product for its particular use. Alkali Scientific shall not be liable for any direct, indirect, consequential or incidental damages arising out of the use, the result of use or the liability to use this product.