IMMOLASE^™ DNA Polymerase

IMMOLASE DNA Polymerase requires a heat-activation step of 10 minutes at 95°C.

As well as most standard applications, IMMOLASE DNA Polymerase is ideally suited to the following: - High-throughput applications - Multiplex PCR - TA Cloning IMMOLASE DNA Polymerase has been manufactured under 13485 Quality Management System and is suitable for further manufacturing use as an IVD component.

The features of IMMOLASE DNA Polymerase are as follows: Heat Activation: 10 minutes at 95°C Speed: 15-30 s/kb (template dependant) Length amplified: Around 5 kb (genomic DNA) Optimal Extension Temperature: 72°C

At Meridian we pride ourselves in supplying high-quality polymerases to suit your requirements. To aid your selection of the most suited enzyme for your specific applications, please see our enzyme selection tool.

All our polymerases are guaranteed for a period of 12 months from the date of purchase. These should be stored at -20°C during this time for optimal retention of activity. Please Note: We do not recommend the storage of our polymerases at -80 °C as ice crystals could form on the active site, which may affect or destroy the activity of the enzyme.

PCR can be a challenging technique, with various parameters to optimize to achieve the best results. If you are having problems, these could be easily resolved by addressing a few issues. Please see our PCR troubleshooting guide for suggestions and help with your specific problems. Observation Recommended Solution(s) No or low PCR yield Enzyme concentration too low – increase the amount of enzyme in 0.5 U increments. Primers degraded – check quality and age of the primers. Magnesium concentration too low – increase concentration in 0.25 mM increments with a starting concentration of 1.75 mM. Primer concentration not optimized. Titrate primer concentration (0.3-1 µM); ensuring that both primers have the same concentration. Template concentration too low – Increase concentration of template. Perform a positive control to ensure that the enzyme, dNTPs and buffers are not degraded and/or contaminated. Multiple Bands Primer annealing temperature too low. Increase annealing temperature. Primer annealing should be at least 5°C below the calculated Tm of primers. Prepare master mixes on ice or use a heat-activated polymerase. For problems with low specificity. Try adding 3% DMSO (not supplied) to improve specificity. Smearing or artifacts Template concentration too high. Prepare serial dilutions of template. Too many cycles. Reduce the cycle number by 3-5 to remove non-specific bands. Enzyme concentration too high - decrease the amount of enzyme in 0.5 U increments. Extension time too long. Reduce extension time in 0.5-1 minute increments.

These terms refer to parameters to be considered when performing PCR and are important features in selecting the correct enzyme for your needs. Understanding what they mean is therefore crucial: Yield: The amount of DNA produced in a PCR reaction. Fidelity: The accuracy of the enzyme at incorporating the correct dNTP to the elongating DNA strand. Processivity: The length of time a polymerase is associated with the template and therefore the size of fragment which can be amplified. Specificity: A measure of the unwanted by-products generated in a reaction.

During PCR setup at room temperature, standard polymerases will have some activity. When using a hot-start polymerase, this enzyme will have no activity at room temperature, thus reducing the risk of unspecific products in the reaction due to these mis-primed oligonucleotides. This feature makes this type of polymerase ideally suited to high-throughput applications, where the reactions may be left sitting at room temperature for prolonged periods of time.

One unit is defined as the amount of enzyme that incorporates 10 nmoles of dNTPs into acid-insoluble form in 30 minutes at 72°C.

All Meridian polymerases are available in the convenient format of a 2x master mix, containing all the reagents and additives necessary to perform successful PCR, with the exception of template, primers and water. This formulation not only provides a convenient and hassle-free PCR setup, but also significantly reduces the chances of human error, inaccuracies and contamination by reducing the pipetting steps required.

The MyTaq HS DNA polymerase works very well with difficult samples like GC rich or bisulfite converted DNA. Especially the hot-start is important, as it decreases primer dimer and unspecific amplification. We would suggest to start with the recommended protocol. If optimization is needed, we would suggest to optimize the annealing temperature. Due to the degraded DNA after bisulfite conversion it may be useful to increase the amount of template and polymerase.

If possible, we would recommend an additional cleanup of affected samples, for instance, customers had very good experiences with the clean-up of samples containing humic acids with SureClean Plus. Alternatively decreasing the template concentration will help to minimize the amount of inhibitors. The amount of primer can be increased, but do not exceed the suggested limits.