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FTAQ-RO

Roche

FastStart Taq DNA Polymerase, 5 U/μl

dNTPs included: no, hotstart, suitable for PCR

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Synonym(s):
PCR, PCR | Taq |polymerase, taq
Enzyme Commission number:

form

liquid

Quality Level

usage

sufficient for ≤1,250 reactions (12032945001)
sufficient for ≤2,500 reactions (12032953001)
sufficient for 1250 reactions
sufficient for ≤250 reactions (12032929001)
sufficient for 250 reactions
sufficient for 2500 reactions
sufficient for ≤50 reactions (12032902001)
sufficient for 50 reactions
sufficient for ≤500 reactions (12032937001)
sufficient for 500 reactions

feature

dNTPs included: no
hotstart

packaging

pkg of 1,000 U (12032937001 [4x250 U])
pkg of 2,500 U (12032945001 [10x250 U])
pkg of 5,000 U (12032953001 [20x250 U])
pkg of 100 U (12032902001)
pkg of 500 U (12032929001 [2x250 U])

manufacturer/tradename

Roche

parameter

72 °C optimum reaction temp.

technique(s)

PCR: suitable

color

colorless

input

purified DNA

pH

8-9

solubility

water: miscible

suitability

suitable for molecular biology

application(s)

genomic analysis
life science and biopharma

storage temp.

−20°C

General description

FastStart Taq DNA Polymerase is a versatile enzyme that can be used in a wide variety of applications and on multiple instrument platforms. This modified, thermostable recombinant Taq DNA polymerase is inactive at temperatures below +75 °C, but is activated by a 2 to 4 minute heat activation step at +95 °C. Since it is inactive at low temperatures, FastStart Taq DNA Polymerase cannot elongate non-specific primer-template hybrids that may form at those temperatures. FastStart Taq DNA Polymerase is an ideal tool for hot start PCR, because the enzyme remains inactive during PCR set-up and prior to the initial denaturation step.

Application

FastStart Taq DNA Polymerase is a thermostable, chemically modified form of recombinant Taq DNA polymerase. The enzyme is inactive at +15 to +25°C during PCR setup, and then activated at +95°C during initial denaturation. This enzyme delivers superior results due to its unique enzyme design and optimized buffer system. FastStart Taq DNA Polymerase is an ideal tool for hot start PCR, because the enzyme remains inactive during PCR set-up and prior to the initial denaturation step.
It can be applied for:
  • PCR
  • Multiplex PCR
  • Difficult templates e.g., secondary structures or GC-rich sequences
  • Automated PCR e.g., handling at room temperatures
  • Hot Start PCR up to 3kb
  • Hot Start RT-PCR up to 3kb
  • Quantitative reverse transcription PCR (RT-qPCR)
  • Bisulfite-specific PCR

Use FastStart Taq DNA Polymerase, dNTPack with ready-to-use PCR nucleotide mix.For maximum convenience, select the 2× concentrated ready-to-use FastStart PCR Master.

Features and Benefits

FastStart Taq DNA Polymerase is a modified recombinant Taq DNA Polymerase, inactive at temperatures below +75°C. The kit includes an optimized PCR buffer and GC-RICH Solution for handling a wide range of templates. High enzyme stability enables pipetting by robotic stations.
  • Higher specificity, sensitivity, and yield:
Hot start PCR makes PCR setup easier.
  • Use robotic setup.
Use this enyzme mix stable for 24hours at +15 to +25°C.
  • Prevent PCR carryover contamination.
Incorporate dUTP and use Uracil-DNA Glycosylase to pretreat PCR master mixes
  • optimized polymerase chain reaction (PCR) buffer system and a GC-RICH solution for handling wide range of templates
  • superior results due to its unique enzyme design and optimized buffer system

Packaging

1 kit containing 5 components

Quality

Each lot is function-tested using human genomic DNA and primers specific for the 365 bp fragment of human tPA gene, and, a 284 bp fragment of the Apo E gene with 74% GC content. Each lot is also tested for the absence of exo- and endonucleases and nicking activity.

Unit Definition

1 μg M13mp9ss DNA, 0.3 μg M13 sequencing primer and 0.1 μCi [α-32P] dCTP are incubated with varying amounts of units of FastStart Taq DNA Polymerase in 50 μl incubation buffer at +65 °C for 60 min. The amount of incorporated dNTPs is determined by trichloroacetic acid precipitation.

Unit Assay: 1 μg M13mp9ss DNA, 0.3 μg M13 sequencing primer and 0.1 μCi [α-32P] dCTP are incubated with varying amounts of units of FastStart Taq DNA Polymerase in 50 μl incubation buffer at +65 °C for 60 min. The amount of incorporated dNTPs is determined by trichloroacetic acid precipitation.

Volume Activity: 5 U/μl

Preparation Note

Storage conditions (working solution): Fast Start Taq mastermix is stable for 4 weeks at -25 °C to -15 °C without primers
Please note: This parameter is not part of specification

Storage and Stability

Keep container tightly closed in a dry and well-ventilated place.

Other Notes

For life science research only. Not for use in diagnostic procedures.

Legal Information

NOTICE TO PURCHASER: LIMITED LICENSE<br />Use of this product is covered by US Patent No. 6,127,155 and corresponding patent claims outside the US.  The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims for using only this amount of product for the purchaser′s own internal research.  No right under any other patent claim and no right to perform commercial services of any kind, including without limitation reporting the results of purchaser′s activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel.  This product is for research use only. Human and veterinary diagnostic uses under Roche patent claims require a separate license from Roche.  All uses other than internal research and human and veterinary diagnostic uses under Roche patent claims require a separate license from Thermo Fisher Scientific. Further information on purchasing licenses from Roche may be obtained by contacting the Licensing Department of Roche Molecular Systems, Inc., 4300 Hacienda Drive, Pleasanton, California 94588, USA or Roche Diagnostics GmbH, Sandhofer Strasse 116, 68305 Mannheim, Germany.  Further information on purchasing licenses from Thermo Fisher Scientific may be obtained by contacting the Licensing Department of  Thermo Fisher Scientific, 5791 Van Allen Way, Carlsbad, California 92008, USA.</ br>NOTICE TO PURCHASER: LIMITED LICENSE<br />Use of this product is covered by US Patent Nos. 5,677,152 and 5,773,258, and corresponding patent claims outside the US.  The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims for using only this amount of product for the purchaser′s own internal research.  No right under any other patent claim and no right to perform commercial services of any kind, including without limitation reporting the results of purchaser′s activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel.  This product is for research use only.  Human and veterinary diagnostic uses under Roche patent claims require a separate license from Roche.  All uses other than internal research and human and veterinary diagnostic uses under Roche patent claims require a separate license from Thermo Fisher Scientific. Further information on purchasing licenses from Roche may be obtained by contacting the Licensing Department of Roche Molecular Systems, Inc., 4300 Hacienda Drive, Pleasanton, California 94588, USA or Roche Diagnostics GmbH, Sandhofer Strasse 116, 68305 Mannheim, Germany.  Further information on purchasing licenses from Thermo Fisher Scientific may be obtained by contacting the Licensing Department of  Thermo Fisher Scientific, 5791 Van Allen Way, Carlsbad, California 92008, USA.
FastStart is a trademark of Roche

Kit Components Only

Product No.
Description

  • FastStart Taq DNA Polymerase, in storage and dilution buffer 5 U/μl

  • PCR Reaction Buffer, with 20 mM MgCl2 10x concentrated

  • PCR Reaction Buffer, without MgCl2 10x concentrated

  • MgCl2 Stock Solution 25 mM

  • GC-RICH Solution 5x concentrated

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

No data available

Flash Point(C)

No data available

Regulatory Information

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Burkhard Malorny et al.
International journal of food microbiology, 117(2), 211-218 (2007-05-22)
A collaborative study including 13 German laboratories was conducted to evaluate the performance of two non-patented real-time PCR methods for the detection of Salmonella in milk powder targeting the ttrC/ttrA- or the invA gene. The enrichment procedure and sample DNA
Whole-body scanning PCR; a highly sensitive method to study the biodistribution of mRNAs, noncoding RNAs and therapeutic oligonucleotides
Boos JA, et al.
Nucleic Acids Research, 41, e145-e145 (2013)
Lucia Carbone et al.
PLoS genetics, 5(6), e1000538-e1000538 (2009-06-27)
Gibbon species have accumulated an unusually high number of chromosomal changes since diverging from the common hominoid ancestor 15-18 million years ago. The cause of this increased rate of chromosomal rearrangements is not known, nor is it known if genome
Sam Kint et al.
Clinical epigenetics, 12(1), 36-36 (2020-03-01)
The HIV-1 proviral genome harbors multiple CpG islands (CpGIs), both in the promoter and intragenic regions. DNA methylation in the promoter region has been shown to be heavily involved in HIV-1 latency regulation in cultured cells. However, its exact role
Genetic mutational testing of Chinese children with familial hematuria with biopsy-proven FSGS
Li Y, et al.
Molecular Medicine Reports, 17, 1513-1526 (2018)

Articles

The choice of the PCR enzyme in combination with an appropriate buffer can profoundly affect PCR outcome.

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.

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