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About This Item
Product Name
FastStart™ High Fidelity PCR System, dNTPack, suitable for PCR, High Fidelity PCR, hotstart, Multiplex PCR
Quality Level
usage
sufficient for ≤200 reactions (04738292001)
sufficient for ≤50 reactions (04738284001)
packaging
pkg of 125 U (04738284001)
pkg of 500 U (04738292001 [2 x 250 U])
manufacturer/tradename
Roche
parameter
72 °C optimum reaction temp.
technique(s)
PCR: suitable
storage temp.
−20°C
Analysis Note
Application
- Hot start PCR
- Multiplex PCR
- Hot Start RT-PCR
- GC-rich template amplification
- Difficult or challenging PCRs
- precapture ligation-mediated PCR (LM-PCR)
- PCR amplification of cDNA 16S rRNA gene
Features and Benefits
- Achieve excellent multiplex performance: For fast high quality results, also use Roche′s PCR Optimization Kit.
- Increase fidelity: Achieve fourfold higher fidelity compared to Taq DNA Polymerase and FastStart Taq DNA Polymerase.
- Amplify challenging DNA: DMSO, a PCR additive, for working with difficult templates, is supplied.
- Cost-effective: Use the convenient premixed solution of PCR grade dNTPs.
General description
Legal Information
Other Notes
- FastStart High Fidelity Enzyme Blend, (5 U/μl) in storage buffer
- FastStart High Fidelity Reaction Buffer, 10x concentrated, with 18 mM MgCl2
- FastStart High Fidelity Reaction Buffer, 10x concentrated, without MgCl2
- MgCl2 Stock Solution, 25 mM
- DMSO
- PCR Nucleotide Mix
Packaging
- FastStart High Fidelity Enzyme Blend, (5 U/μl) in storage buffer
- FastStart High Fidelity Reaction Buffer, 10x concentrated, with 18mM MgCl2
- FastStart High Fidelity Reaction Buffer, 10x concentrated, without MgCl2
- MgCl2 Stock Solution, 25mM
- DMSO
- PCR Nucleotide Mix (each dNTPack contains the 10mM additive-free sodium salt nucleotides in a ready-to-use mix)
Preparation Note
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
203.0 °F
flash_point_c
95 °C
Regulatory Information
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The purpose of Hot Start PCR is to inhibit the PCR reaction in order to reduce nonspecific amplification, prevent the formation of primer dimers, and increase product yields.
热启动PCR的目的在于抑制PCR反应,从而减少非特异性扩增、防止引物二聚体形成并提高产物产量。
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