- Robust - enzyme blend and buffer system promotes reliable amplification of the most challenging and complex targets, even in the presence of inhibitors
- Sensitive - improved target affinity and high processivity ensure successful amplification in low-copy number assays
- Efficient - high-yield amplification of a broad range of targets up to 10 kb including complex DNA extracted from human, animal and plant samples
- Specific - an antibody-mediated hot-start blend that remains completely inactive during PCR set-up to prevent non-specific amplification
- Convenient - advanced buffer system minimizes the requirements for PCR optimization thereby reducing time to results and eliminating the cost of unnecessary repeats
- Accurate - proofreading component delivers 3.5x higher fidelity than Taq DNA Polymerase, enabling cloning of PCR products
MyFi™ has been developed to give reliable amplification of targets up to 10 kb from challenging and complex targets. MyFi shows improved tolerance to PCR inhibitors, thereby enabling reliable detection from samples from which DNA is difficult to purify. Furthermore a unique buffer system and enzyme blend promote highly sensitive amplification, ideal for low-copy number targets. The inclusion of MyTaq HS means MyFi generates PCR products with 3’-A overhangs making it suitable for TA cloning. MyFi has the added convenience of room temperature reaction assembly, to avoid non-specific amplification and primer-dimer formation.
An advanced buffer system and enzyme blend combine to give increased target affinity, ideal for amplification of cDNA libraries, complex genomic fragments and GC-rich targets.
- Amplification of challenging and complex templates
- Inhibitor-tolerant PCR
- Robust PCR
- Longer PCR (up to 10 kb)
- Low-copy PCR
- Higher-fidelity PCR (NGS library amplification)
- TA cloning
We commonly use the Bioline MyFi polymerase, and it works better than any other polymerase. MyFi polymerase could amplify complicated short tandem repeat sequences (STR or SSR / microsatellite) better than any other kit.
Hiroshi Shinozuka, AgriBio, Bundoora, Australia
Product SelectionPlease refer to the PCR Selection Chart to confirm the recommended product for your PCR application.
Certification of Analysis (COAs)
MyFi DNA Polymerase
1 x 125 µL
1 x 250 µL
2 x 625 µL
5x MyFi Reaction Buffer
1 x 625 µL
1 x 1.25 mL
5 x 1.25 mL
BIO-21117: 125 x 25 µL Reactions: 1 x 125 µL
BIO-21118: 250 x 25 µL Reactions: 1 x 250 µL
BIO-21119: 1250 x 25 µL Reactions: 2 x 625 µL
Storage & Stability
All components should be stored at -20°C upon receipt for optimum stability. Repeated freeze/thaw cycles should be avoided.
When stored under the recommended conditions and handled correctly, full activity of the reagents is retained until the expiry date indicated on the outer box label.
On Dry Ice or Blue Ice.
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.
|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.|