Taq DNA Polymerase, 1 U/μl
ROCHE/TAQL-RO - suitable for PCR, hotstart: no, dNTPs included: no
Synonym: dna amplification; pcr; polymerase; primer extension
Product Type: Chemical
| application(s) | genomic analysis life science and biopharma |
| biological source | bacterial (Thermus aquaticus BM) |
| color | colorless |
| concentration | 25 U/mL |
| 30 U/mL | |
| feature | dNTPs included: no |
| hotstart: no | |
| foreign activity | Endonucleases 20 units, none detected |
| Nicking activity 20 units, none detected | |
| form | liquid |
| input | purified DNA |
| manufacturer/tradename | Roche |
| mol wt | ~95 kDa |
| NCBI accession no. | AAA27507 AAA27507   |
| optimum pH | ~9.0 (20 °C) |
| packaging | pkg of 1,000 U (11647687001 [4 x 250 U]) |
| pkg of 250 U (11647679001) | |
| parameter | 72 °C optimum reaction temp. |
| Quality Level | 100 |
| recombinant | expressed in E. coli |
| solubility | water: miscible |
| specific activity | 1 U/μL |
| storage temp. | −20°C |
| suitability | suitable for molecular biology |
| suitable for PCR | |
| technique(s) | PCR: suitable |
| UniProt accession no. | P19821 |
| usage | sufficient for ≤2,000 reactions (11647687001) |
| sufficient for ≤500 reactions (11647679001) |
| Application: | This lower concentration of our recombinant Taq DNA Polymerase allows small amounts of the polymerase to be pipetted more accurately and conveniently. In all other respects, this preparation is identical to our higher concentration (5 U/μl) preparation and can be used for: • PCR • RT-PCR • Other primer-extension reactions, such as sequencing and labeling |
| General description: | The enzyme was cloned in E.coli and is isolated to be free of unspecific endo- or exonucleases according to the current quality control procedurese. Taq DNA Polymerase is a highly processive 5′–3′ DNA polymerase that lacks 3′–5′ exonuclease activity. It consists of a single polypeptide chain with a molecular weight of approximately 95 kDa. The enzyme exhibits highest activity at a pH of around 9 (adjusted at 20 °C) and temperatures around +75 °C. Taq DNA Polymerase also accepts modified deoxyribonucleosidetripho The high processivity, absence of exonuclease activity and temperature optima of Taq DNA Polymerase enable the use of this enzyme in DNA sequencing, especially where the resolution of secondary structures plays a major role. |
| Legal Information: | Use of this product is covered by US patent claims 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, no right to perform any patented method, 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. Diagnostic uses under Roche patent claims require a separate license from Roche. Further information on purchasing licenses may be obtained by contacting the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA. |
| Other Notes: | For life science research only. Not for use in diagnostic procedures. |
| Packaging: | 1 kit containing 4 components |
| Unit Definition: | One unit Taq DNA Polymerase is defined as the amount of enzyme that incorporates 10 nmol of total deoxyribonucleoside triphosphates into acid precipitable DNA within 60 min at +65 °C under the assay conditions stated above. 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 |
| activity | specific activity: 1 U/μL |
| Storage Temp. | −20°C |
| Enzyme Commission (EC) Number | 2.7.7.7 ( BRENDA | IUBMB ) |
| UNSPSC | 41106300 |
| Components | Taq DNA Polymerase 1 U/μl; PCR Buffer with MgCl<sub>2</sub> 10x concentrated; MgCl<sub>2</sub> Stock Solution; PCR Buffer without MgCl<sub>2</sub> |