PWOPOL-RO
Roche
Pwo DNA Polymerase
Synonym(s):
polymerase, dna, pwo
About This Item
Recommended Products
biological source
microbial (Pyrococcus woesei)
Quality Level
form
liquid
usage
sufficient for ≤200 reactions (11644955001)
sufficient for 200 reactions
sufficient for ≤40 reactions (11644947001)
sufficient for 40 reactions
specific activity
≥5000 U/mL
mol wt
90 kDa
feature
High Fidelity PCR
dNTPs included: no
hotstart: no
packaging
pkg of 100 U (11644947001)
pkg of 500 U (11644955001 [2 x 250 U])
manufacturer/tradename
Roche
concentration
2.5 units/reaction
technique(s)
PCR: suitable
color
colorless
input
purified DNA
solubility
water: soluble
suitability
suitable for enzyme test
application(s)
genomic analysis
life science and biopharma
foreign activity
Endonucleases with lambda-DNA 30 units, none detected
Nicking act using pBR322-DNA ≤30 units, none detected
storage temp.
−20°C
Related Categories
General description
The use of Pwo DNA Polymerase during PCR significantly reduces the occurrence of random amplification errors.
Application
- Due to its proofreading activity, the thermostable Pwo DNA Polymerase has an extremely low error rate, 18-fold lower compared to Taq DNA Polymerase. It is therefore ideal for applications that require the highest possible fidelity in DNA synthesis. It can be applied for High fidelity PCR
- Cloning of PCR products
- Characterization of rare mutations
- PCR
Features and Benefits
- Excellent accuracy (18-fold more accurate than Taq DNA polymerase)
- High thermal stability
- Nearly as processive as Taq DNA polymerase
- Accepts modified nucleotides
Packaging
Quality
- Activity: The enzyme is tested on activated DNA.
- Function: The enzyme is tested in two PCRs, using λDNA and human genomic DNA as templates.
- Proofreading ability: Proofreading activity is assayed according to the laq Iq fidelity assay [Frey, B. & Suppmann, B. (1995) Biochemica 2. 8-9].
- Absence of nucleases: The enzyme is tested on various substrates to ensure the absence of detectable endonucleases, exonucleases, and nicking activity according to the current Quality Control procedures.
Unit Definition
Unit Assay: Incubation buffer for assay on activated DNA
20 mM Tris-HCl, pH 8.8 (20 °C), 50 mM KCl, 2.5 mM MgCl2, 10 mM 2-mercaptoethanol, 0.2 mM of each dATP, dCTP, dGTP, dTTP.
Incubation procedure
12.5 mg activated calf thymus DNA and 0.1 mCi [α-32P]dCTP are incubated with 0.01 to 0.1 U Pwo DNA Polymerase in 50 μl incubation buffer with a paraffin oil overlay at +70 °C for 30 minutes. The amount of incorporated dNTPs is determined by trichloroacetic acid precipitation followed by scintillation counting.
Volume Activity: 5 U/μl
Preparation Note
Modified nucleotides are substrates
Pwo DNA Polymerase accepts modified nucleotides like digoxigenin-dUTP, biotin-dUTP, or fluorescein-dUTP. Thus, it can add these nucleotides to DNA during PCR. These nonradioactively labeled products can be used as a hybridization probe in many applications.
Magnesium concentration
If you use the magnesium-containing reaction buffer supplied with the enzyme, the final MgCl2 concentration in the PCR will be 2.0mM. For other magnesium concentrations (e.g., for optimizing the reaction to accommodate a particular template), use the magnesium-free reaction buffer and add appropriate amounts of the magnesium stock.
Storage and Stability
kept upright to prevent leakage
Other Notes
Legal Information
Kit Components Only
- Enzyme is supplied in storage and dilution buffer
- PCR buffer, with 20 mM MgSO4 10x concentrated
- PCR buffer, without MgSO4 10x concentrated
- MgSO4 stock solution
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 2
Flash Point(F)
does not flash
Flash Point(C)
does not flash
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Global Trade Item Number
SKU | GTIN |
---|---|
11644955001 | 4061838704382 |
11644947001 | 4061838704375 |
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