DescriptionUnique blend of highly-efficient MyTaq HS DNA Polymerase and a proprietary proofreading enzyme that combine to give increased target affinity for use with challenging templates and inhibitor-rich samples.Product HighlightsRobust - enzyme blend and buffer system promotes reliable amplification of the most challenging and complex targets, even in the presence of inhibitorsSensitive - improved target affinity and high processivity ensure successful amplification in low-copy number assaysEfficient - high-yield amplification of a broad range of targets up to 10 kb including complex DNA extracted from human, animal and plant samplesSpecific - an antibody-mediated hot-start blend that remains completely inactive during PCR set-up to prevent non-specific amplificationConvenient - advanced buffer system minimizes the requirements for PCR optimization thereby reducing time to results and eliminating the cost of unnecessary repeatsAccurate - proofreading component delivers 3.5x higher fidelity than Taq DNA Polymerase, enabling cloning of PCR productsProduct DescriptionMyFi™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. Request InfoApplicationsAmplification of challenging and complex templatesRobust PCRLonger PCR (up to 10 kb)Low-copy PCRTA cloning Greater reliability with GC-rich DNAA 525 bp fragment of the 62% GC-rich human epidermal growth factor receptor (EGFR) gene (A), a 750 bp fragment of the 64% GC-rich translation factor p64 (myc) gene (B), a 900 bp fragment of 43% GC-rich angiotensin II receptor type I (AGTR1) gene (C), a 1.2 kb fragment of 62% GC-rich EGFR gene (D) were amplified using MyFi DNA Polymerase and similar polymerases from other suppliers. A five-fold serial dilution of human genomic DNA (25 ng - 8 pg, 1.6 pg and 0 pg, lanes 1-8 respectively) was used as template. Marker is HyperLadder 1kb (M). The results demonstrate that that MyFi delivers more reliable amplification of challenging targets. Amplification of complex DNA up to 10kbA 3.9 kb fragment of a-1-antitrypsin (AT-R3) gene (A), and a 7.0 kb (B), 9.0 kb (C) and 10.0 kb (D) fragment of human (ß-globin) HbG gene, were amplified using MyFi DNA Polymerase and similar DNA Polymerases from other suppliers. A serial dilution of human genomic DNA (5 ng, 1 ng, 200 pg, 40 pg, 8 pg, 1.6 pg, 0.32 pg and 0 pg, Lanes 1-8 respectively) was used as template. Marker is HyperLadder 1kb (M). The results demonstrate that MyFi can be used to amplify targets up to 10 kb from even very challenging templates.PCR Enzyme Guide Download the PCR Enzyme Guide with detailed product descriptions and performance data to help you choose the best product for your research PCR Selection Chart Select the best reagent for your research