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Taq DNA Polymerase (1 U/μl), dNTPack

ROCHE/TAQNL-RO - suitable for PCR, optimum pH ~9.0 (20 °C)

Synonym: Taq | PCR | DNA amplification

Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-4738225001 250 units
$0.00
1/EA
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45-4738241001 1000 units
$798.00
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feature dNTPs included
  hotstart: no
input purified DNA
manufacturer/tradename Roche
optimum pH ~9.0 (20 °C)
packaging pkg of 1,000 U (04738241001 [4 x 250 U])
  pkg of 250 U (04738225001)
parameter 72 °C optimum reaction temp.
Quality Level 100 
storage temp. −20°C
technique(s) PCR: suitable
usage sufficient for ≤2,000 reactions (04738241001)
  sufficient for ≤500 reactions (04738225001)
Application: Taq DNA Polymerase (1 U/μl), dNTPack may be used for:
• PCR
• RT-PCR
• Other primer-extension reactions, such as sequencing and labeling
General description: Taq DNA Polymerase (1 U/μl), dNTPack, comprises Taq DNA Polymerase and a ready-to-use solution of PCR grade nucleotides. Taq DNA polymerase is a highly processive 5′-3′ DNA polymerase that lacks 3′–5′ exonuclease activity. It is stable during prolonged incubations at elevated temperatures (+95 °C). Additionally, it exhibits highest activity at a pH of around 9 (adjusted at 20 °C) and temperatures around +75 °C. It accepts dNTP analogs as substrates. There is no difference in stability or performance when compared to the standard concentration of Taq DNA Polymerase.
Other Notes: For life science research only. Not for use in diagnostic procedures.
Packaging: 1 kit containing 5 components
Unit Definition: One unit Taq DNA Polymerase is defined as the amount of enzyme that incorporates 10 nmol of total deoxyribonucleosidetriphosphates into acid precipitable DNA within 30 minutes at +75 °C under the assay conditions stated under unit assay.

Unit Assay: Incubation buffer:
67 mM Tris/HCl; pH 8.3/25 °C, 5 mM MgCl2, 10 mM Mercaptoethanol, 0.2% Polydocanol, 0.2 mg/ml Gelatine, 0.2 mM each dATP, dGTP, dTTP and 0.1 mM dCTP.

Incubation procedure:
M13mp9ss, M13 primer (17mer) and 1 μCi (α-32P) dCTP are incubated with suitable dilutions of Taq DNA Polymerase in 50 μl incubation buffer at +65 °C for 60 minutes. The amount of incorporated dNTPs is determined by trichloroacetic acid precipitation.

Volume Activity: 1 U/μl
Hazard statements H412
Precautionary statements P273 - P501
RIDADR NONH for all modes of transport
WGK Germany WGK 2
Flash Point(F) does not flash
Flash Point(C) does not flash
Storage Temp. −20°C
Enzyme Commission (EC) Number 2.7.7.7   ( BRENDA  | IUBMB  )
UNSPSC 41106300
Components Taq DNA Polymerase; PCR Buffer with MgCl<sub>2</sub> 10x concentrated; MgCl<sub>2</sub> Stock Solution; PCR Buffer without MgCl<sub>2</sub>; PCR Nucleotide Mix</ul>

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