HomePolymerase Chain Reaction ApplicationsAmplification of DNA Using Jumpstart™ Taq DNA Polymerase (D9307)

Amplification of DNA Using Jumpstart™ Taq DNA Polymerase (D9307)


Note: JumpStart™ Taq DNA polymerase has been shown to work effectively with up to 5% v/v DMSO. Other co-solvents, solutes (e.g., salts) and extremes in pH or other reaction conditions may reduce the affinity of the JumpStart™ Taq antibody for the Taq DNA polymerase and thereby compromise its effectiveness.

Preparation of PCR Master Mix and Thermal Cycling Parameters

Because the Taq DNA polymerase is a magnesium ion-dependent enzyme, the optimal conditions for the concentration of Taq, template DNA, primers, and MgCl2 will depend on the system being utilized. It may be necessary to determine the optimal conditions for each individual component. This is especially true for the JumpStart™ Taq, cycling parameters, and the MgCl2 concentration. It is recommended the enzyme and the MgCl2 be titrated to determine the optimal efficiency.

To minimize tube-to-tube variation, preparation of a PCR master mix with JumpStart™ Taq is recommended. The amount prepared should be based on the number of PCR reactions to be performed.

1. For a single reaction, add the following reagents to a 0.2 or 0.5 mL microtubes in the following order:

*The individual nucleotides (1 µL of each 10 mM solution, 4 µL total) may be replaced by 1 µL of Deoxynucleotide Mix, Catalog Number D7295.

2. Mix gently and briefly centrifuge to collect all solution at the bottom of the tube.

3. Add 50 µL of mineral oil to the top of each tube to prevent evaporation (optional, depending on the model of thermal cycler).

4. Amplification parameters will vary depending on the primers and the thermal cycler used. It may be necessary to optimize the system for individual primers, template, and thermal cycler.

Typical cycling parameters:

* 1 minute minimum or 1 minute per kb expected amplicon.

5. The amplified DNA can be evaluated by agarose gel electrophoresis and subsequent ethidium bromide staining. Mineral oil overlay may be removed by a single chloroform extraction (1:1), recovering the aqueous phase.

Troubleshooting Guide



No license is conveyed with the purchase of this product under any of US Patents Nos. 5,804,375, 5,994,056, 6,171,785, 6,214,979, 5,538,848, 5,723,591, 5,876,930, 6,030,787, and 6,258,569, and corresponding patents outside the United States, or any other patents or patent applications, relating to the 5’ Nuclease and dsDNA-Binding Dye Processes. For further information contact the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA.