FTAQ-RO
Roche
FastStart™ Taq DNA Polymerase, 5 U/μl
dNTPs included: no, hotstart, suitable for PCR
About This Item
Recommended Products
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
Application
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
- Higher specificity, sensitivity, and yield:
- Use robotic setup.
- Prevent PCR carryover contamination.
- 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
Quality
Unit Definition
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
Please note: This parameter is not part of specification
Storage and Stability
Other Notes
Legal Information
Kit Components Only
- 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
12 - Non Combustible Liquids
wgk_germany
WGK 1
flash_point_f
No data available
flash_point_c
No data available
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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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