TransStart® FastPfu Fly DNA Polymerase

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Catalog Number:AP231-21

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Description

TransStart® FastPfu Fly DNA Polymerase is a hot start, ultra high-fidelity DNA Polymerase used for fast PCR. Compared with TransStart® FastPfu DNA Polymerase, TransStart® FastPfu Fly DNA Polymerase has higher extension rate (≤ 5 kb fragments can achieve 12 kb/min extreme amplification, > 5 kb fragments can achieve 6 kb/min high-speed amplification), featuring higher amplification efficiency, higher yield, higher fidelity and higher sensitivity. 2×TransStart® FastPfu Fly Reaction Mix already contains dNTPs. When DNA is amplified, just add template, primer, water and TransStart® FastPfu Fly DNA Polymerase. The Reaction can be carried out with the concentration of Reaction Mix being 1×. PCR products are blunt end and

can be cloned directly into pEASY®-Blunt series of vectors.

• Offers 108-fold fidelity as compared to EasyTaq® DNA Polymerase.

• PCR products are blunt end and can be cloned directly into pEASY®-Blunt series of vectors.

• Amplification of genomic DNA fragment up to 15 kb.

• Amplification of plasmid DNA fragment up to 20 kb.

Features

• Hot start, high specificity.

• High amplification efficiency.

• Fast and ultra high-fidelity.

• High sensitivity.

• High yield.

Applications

• Complex templates, GC/AT-rich templates.

• Ultra high-fidelity and fast PCR, blunt end cloning, site-directed mutagenesis.

• Long fragment amplification.

Storage

at -18°C or below for two years

Shipping

Dry ice (-70 ℃)

Product Composition
Component    AP231-21    AP231-22    AP231-23
TransStart® FastPfu Fly DNA Polymerase            250 U×1           500 U×1           500 U×6
TransStart® FastPfu Fly Reaction Mix              1 ml×3          1.2 ml ×5        1.2 ml ×30
50 mM MgSO4           200 μl×1          400 μl ×1             1 ml ×1
6×DNA Loading Buffer           500 μl×1             1 ml ×1             1 ml ×2
PCR Stimulant           200 μl×1           400 μl×1             1 ml ×1
References

1 Zhang A, Shan T, Sun Y, et al. Directed evolution rice genes with randomly multiplexed sgRNAs assembly of base editors[J]. Plant Biotechnology Journal, 2023.(IF 13.80)

2 Xu Y, Zhu T F. Mirror-image T7 transcription of chirally inverted ribosomal and functional RNAs[J]. Science, 2022.(IF 63.714)

3 Wang D, Yan F, Wu P, et al. Global profiling of regulatory elements in the histone benzoylation pathway[J]. Nature Communications, 2022.(IF 14.919)

4 Niu L, Shen W, Shi Z, et al. Three-dimensional folding dynamics of the Xenopus tropicalis genome[J]. Nature Genetics, 2021.(IF 38.33)

5 Jin S, Fei H, Zhu Z, et al. Rationally designed APOBEC3B cytosine base editors with improved specificity[J]. Molecular cell, 2020.(IF 15.58)

6 Chen J, Ou Y, Yang Y, et al. KLHL22 activates amino-acid-dependent mTORC1 signalling to promote tumorigenesis and ageing[J]. Nature, 2018.(IF 40.13)

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