PWOPOL-RO
Roche
Pwo DNA Polymerase
Sinonimo/i:
polymerase, dna, pwo
About This Item
Prodotti consigliati
Origine biologica
microbial (Pyrococcus woesei)
Livello qualitativo
Stato
liquid
impiego
sufficient for ≤200 reactions (11644955001)
sufficient for 200 reactions
sufficient for ≤40 reactions (11644947001)
sufficient for 40 reactions
Attività specifica
≥5000 U/mL
PM
90 kDa
Caratteristiche
High Fidelity PCR
dNTPs included: no
hotstart: no
Confezionamento
pkg of 100 U (11644947001)
pkg of 500 U (11644955001 [2 x 250 U])
Produttore/marchio commerciale
Roche
Concentrazione
2.5 units/reaction
tecniche
PCR: suitable
Colore
colorless
input
purified DNA
Solubilità
water: soluble
Compatibilità
suitable for enzyme test
applicazioni
genomic analysis
life science and biopharma
Attività estranea
Endonucleases with lambda-DNA 30 units, none detected
Nicking act using pBR322-DNA ≤30 units, none detected
Temperatura di conservazione
−20°C
Categorie correlate
Descrizione generale
The use of Pwo DNA Polymerase during PCR significantly reduces the occurrence of random amplification errors.
Applicazioni
- 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
Caratteristiche e vantaggi
- Excellent accuracy (18-fold more accurate than Taq DNA polymerase)
- High thermal stability
- Nearly as processive as Taq DNA polymerase
- Accepts modified nucleotides
Confezionamento
Qualità
- 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.
Definizione di unità
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
Nota sulla preparazione
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.
Stoccaggio e stabilità
kept upright to prevent leakage
Altre note
Note legali
Solo come componenti del kit
- 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
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Aquatic Chronic 3
Codice della classe di stoccaggio
12 - Non Combustible Liquids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
does not flash
Punto d’infiammabilità (°C)
does not flash
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