Choose Bioline MyTaq for superior performance and greater value!

Is your current supplier making you re-evaluate your polymerase? If so, this is the ideal time to take a step up in performance and value.

Choose Bioline MyTaq DNA Polymerase for faster reaction times, higher sensitivity and higher yields, meaning quicker results, fewer repeats and greater value from your precious resources.
  • Hot-Start for increased specificity
  • Fast PCR in under 30 minutes
  • High sensitivity to detect low copy number samples
  • High yields to make your samples go further
  • Perfect for complex templates
MyTaq DNA Polymerase is available in a range of formats and options to suit your applications, all of which use the latest technology in PCR enzyme design. MyTaq is engineered to increase affinity for DNA and is supplied with an industry leading buffer formulation loaded with dNTPs, MgCl2 and enhancers at optimal concentrations. The pre-optimized configuration of MyTaq removes the need to optimize individual reactions and delivers superior amplification time after time.

MyTaq Conversion Chart

Current Polymerase

Use Bioline MyTaq

Hot Start DNA Polymerase MyTaq™ HS DNA Polymerase
Hot Start Colored Master Mix MyTaq™ HS Red Mix
Hot Start Colorless Master Mix MyTaq™ HS Mix
Colored DNA Polymerase MyTaq™ Red DNA Polymerase
DNA Polymerase MyTaq™ DNA Polymerase
Colored Master Mix MyTaq™ Red Mix
Colorless Master Mix MyTaq™ Mix

MyTaq Displays Higher Yield & Sensitivity

Amplification of a 525bp fragment of EGFR (upper row) and a 750bp fragment of Myc (lower row) from a serial dilution of human genomic DNA under identical cycling conditions (following manufacturers recommended protocol).

Amplification of a 525bp fragment of EGFR (upper row) and a 750bp fragment of Myc (lower row) from a serial dilution of human genomic DNA under identical cycling conditions (following manufacturers recommended protocol).

Conclusion: MyTaq demonstrates higher yield and better sensitivity than both the original and new formulations.

 

MyTaq is Faster and More Robust

Amplification of a 1200bp fragment of EFGR (62% GC) (upper row) and 1200bp fragment of ATPase (40% GC) (lower row)  from a serial dilution of human genomic DNA under identical cycling conditions (following manufacturers recommended protocol).

Amplification of a 1200bp fragment of EFGR (62% GC) (upper row) and 1200bp fragment of ATPase (40% GC) (lower row) from a serial dilution of human genomic DNA under identical cycling conditions (following manufacturers recommended protocol).

Conclusion: MyTaq clearly outperforms the original and new formulations of GoTaq® with both high and low GC content templates, demonstrating greater speed and robustness.

Enzymes used for comparisons:
1) MyTaq™ HS Mix
2) New GoTaq® G2 Hot Start Colorless MasterMix
3) Original GoTaq® Hot Start Colorless MasterMix.

Request a MyTaq Sample

Upgrade your PCR performance by switching to MyTaq DNA Polymerase. Request a free sample and see for yourself how MyTaq DNA Polymerase can accelerate and improve your research. If you have an existing account with us please log in to auto-fill the form.

If you're running MyTaq in parallel with your existing supplier, submit your results as part of our global PCR Challenge and receive a free Bioline t-shirt* for your efforts. You can see other PCR Challenge research data here.

* Subject to availability.

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GoTaq® is a registered trademark of Promega Corporation in U.S.A. and/or other countries.
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