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Taq Pol Thermostable DNA polymerase | |  |
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S pack |
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PCR-202S |
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200 units |
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35,00 |
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L pack |
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PCR-202L |
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1000 units |
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140,00 |
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 | Store at -20°C, avoid frequent thawing and freezing
Taq Pol (5 units/µl)
10x Taq reaction buffer complete
10x Taq reaction buffer without MgCl2
MgCl2 stock solution |  | Taq Pol is recommended for use in routine PCR reactions. It is optimized for high specificity and guarantees minimal by-product formation. The buffer system is particularly suitable for plate based PCR and automated pipetting where a detergent free buffer system is required.
The enzyme replicates DNA at 72°C. It catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction in the presence of magnesium. It also possesses a 5'→3' polymerization-dependent exo-nuclease replacement activity but lacks a 3'→5' exonuclease activity. |  |
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Taq Pol / high yield Thermostable DNA polymerase | |  |
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S pack |
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PCR-201S |
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200 units |
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35,00 |
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L pack |
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PCR-201L |
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1000 units |
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140,00 |
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Taq Pol (5 units/µl)
10x High yield buffer complete
10x High yield buffer without MgCl2
MgCl2 stock solution |  | Taq Pol / high yield is recommended for use in routine PCR reactions. The buffer system is optimized for high efficiency and gives superior amplification results in a broad range of reaction conditions with most primer-template pairs. The buffer system facilitates the incorporation of labeled or modified nucleotides into DNA. Note that the ammonium based buffer system contains detergent and is not recommended for plate based PCR and automated pipetting.
The enzyme replicates DNA at 72°C. It catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction in the presence of magnesium. It also possesses a 5'→3' polymerization-dependent exo-nuclease replacement activity but lacks a 3'→5' exonuclease activity. |  |
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Hot Start Pol Heat-activatable DNA polymerase for high specificity | |  |
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S pack |
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PCR-203S |
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200 units |
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70,00 |
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L pack |
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PCR-203L |
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1000 units |
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280,00 |
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Hot Start Pol (5 units/µl)
10x Hot start buffer complete
10x Hot start buffer without MgCl2
MgCl2 stock solution |  | Hot Start Pol provides improved specificity and sensitivity when amplifying low-copy-number targets in complex backgrounds or when prolonged room-temperature set up is required. The polymerase activity is blocked at ambient temperature and switched on automatically at the onset of the initial denaturation. The thermal activation prevents the extension of nonspecifically annealed primers and primer-dimer formation at low temperatures during PCR setup.
The enzyme catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction in the presence of magnesium. It also possesses a 5'→3' polymerization-dependent exonuclease replacement activity but lacks a 3'→5' exonuclease activity.
Activation step
Hot Start Pol requires no prolonged heating or denaturing step. The polymerase inhibiting ligand is quickly released at the increased temperature of thermal cycling. |  |
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High Fidelity Pol Thermostable DNA polymerase for high accuracy | |  |
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Amount |
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Price (EUR) |
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Buy |
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S pack |
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PCR-204S |
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100 units |
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48,00 |
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L pack |
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PCR-204L |
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500 units |
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192,00 |
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High Fidelity Pol (2.5 units/µl)
10x High fidelity buffer |  | High Fidelity Pol is based on a blend of Taq DNA polymerase and a proofreading enzyme specially designed for highly accurate and efficient amplification. It shows excellent results with extremely long (up to 30 kb), GC-rich or other difficult templates.
The enzyme blend includes a highly processive 5'→3' DNA polymerase and possesses a 5'→3' polymerization-dependent exonuclease replacement activity. Its inherent 3'→5' exonuclease proofreading activity results in a greatly increased fidelity of DNA synthesis compared to Taq polymerase.
The enzyme is highly purified and free of bacterial DNA. |  |
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Pfu-X Polymerase Proofreading DNA polymerase for highest accuracy | |  |
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Cat. No. |
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Amount |
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Price (EUR) |
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Buy |
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S pack |
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PCR-207S |
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100 units |
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60,00 |
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L pack |
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PCR-207L |
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500 units |
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240,00 |
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