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Engineered for NGS library amplification, Twist TrueAmp Polymerase delivers uniform coverage across GC extremes, high sensitivity from low inputs, and automation ready hot start performance.
Amplify uniformly across extreme 5–95% GC regions to maintain coverage of difficult targets. Improved fidelity and reduced homopolymer slippage deliver cleaner data and more confident calls with fewer repeats.
Generate consistent, high-yield libraries from complex samples—even at ≤100 pg input—so you recover more usable data and keep your workflows moving forward.
An aptamer enabled hot start enables room temperature stability for automation, while a single-tube 2× mastermix simplifies setup and reduces hands-on time; helping you scale workflows with fewer errors and faster turnaround.
TrueAmp sustains coverage where others drop out, improving sequencing economics and preserving difficult targets.
With improved efficiency, TrueAmp can hit yield targets in fewer cycles, limiting cycle-induced artifacts. It remains robust for low-yield libraries typical of post-capture PCR.
An engineered proofreading polymerase reduces C→T misincorporations often caused by cytosine deamination and limits slippage across long homopolymers—critical for sensitive variant detection.
Magnetic beads are widely used for purification and size selection but can inhibit PCR and lower yields.
TrueAmp sustains coverage where others drop out, improving sequencing economics and preserving difficult targets.
Figure 1 GC-normalized coverage; AT-rich C. difficile and GC-rich B. pertussis.
With improved efficiency, TrueAmp can hit yield targets in fewer cycles, limiting cycle-induced artifacts. It remains robust for low-yield libraries typical of post-capture PCR.
Figure 2. Serial dilutions from 1 ng to 100 fg, Qubit and TapeStation QC.
An engineered proofreading polymerase reduces C→T misincorporations often caused by cytosine deamination and limits slippage across long homopolymers—critical for sensitive variant detection.
Figure 3. Substitution rates after >7M base incorporations; homopolymer readout using Twist clonal plasmids.
Magnetic beads are widely used for purification and size selection but can inhibit PCR and lower yields.
Figure 4. Tolerance to Paramagnetic Beads During PCR. PCR reactions were spiked with 6.25 μl, 12.5 μl, 25 μl, and 50 μl of MyOne T1 Beads, M270 Beads (Invitrogen), and Twist DNA Purification Beads. Reactions were purified post bead-removal and quantified on Qubit dsDNA Broad Range Assay.
TrueAmp sustains coverage where others drop out, improving sequencing economics and preserving difficult targets.
With improved efficiency, TrueAmp can hit yield targets in fewer cycles, limiting cycle-induced artifacts. It remains robust for low-yield libraries typical of post-capture PCR.
An engineered proofreading polymerase reduces C→T misincorporations often caused by cytosine deamination and limits slippage across long homopolymers—critical for sensitive variant detection.
Magnetic beads are widely used for purification and size selection but can inhibit PCR and lower yields.
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