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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.
Figure 1 GC-normalized coverage; AT-rich C. difficile and GC-rich B. pertussis.
Figure 2. Serial dilutions from 1 ng to 100 fg, Qubit and TapeStation QC.
Figure 3. Substitution rates after >7M base incorporations; homopolymer readout using Twist clonal plasmids.
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.
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