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AmpliTaq Gold DNA Polymerases |
Applied Biosystems AmpliTaq DNA Polymerases are recombinant Taq DNA Polymerases used in standard research applications such as routine PCR, genotyping, and colony PCR. The AmpliTaq DNA Polymerases are available in different formulations—AmpliTaq DNA polymerase, AmpliTaq 360 DNA polymerase, AmpliTaq Gold DNA polymerase, and AmpliTaq Gold 360 DNA Polymerase.
While AmpliTaq 360 and AmpliTaq DNA Polymerase are recombinant Taq polymerases, AmpliTaq Gold and AmpliTaq Gold 360 DNA Polymerases are hot-start polymerases. These hot-start enzymes use a chemical modification to inhibit enzyme activity at room temperature. Upon activation, the modifier is released and the enzyme is activated. The activation temperature is typically above the primer annealing temperature, which helps ensures specific priming.
Watch the video on how Amplitaq Gold DNA Polymerases work.
While both AmpliTaq Gold formats are designed for hot-start reactions, the AmpliTaq Gold 360 DNA Polymerase is more versatile because it can better handle GC-rich templates and is more flexible for shipping, storage, and handling. Compared to the original AmpliTaq Gold DNA Polymerase, AmpliTaq Gold 360 DNA Polymerase is purified by an additional process which reduces residual bacterial DNA sequences from the enzyme. When used with the 360 Gold Buffer, this ultra-pure enzyme, in addition to its hot-start capabilities, reduces false positive results, amplifies low-level target sequences, and promotes the amplification of a variety of templates including those from bacterial and human genomes.
| AmpliTaq Gold 360 DNA Polymerase | AmpliTaq Gold DNA Polymerase | Platinum II Taq Hot-Start DNA Polymerase |
---|---|---|---|
Hot-start modification | Chemical | Chemical | Antibody |
Enzyme activation time | 10 min | 10 min | 2 min |
Universal annealing temperature of 60°C | No | No | Yes |
DNA synthesis speed | 60 sec/kb | 60 sec/kb | 15 sec/kb |
Amplification length | Up to 5 kb | Up to 5 kb | Up to 5 kb |
Inhibitor tolerance | No | No | Yes |
GC-rich DNA amplification | ++ | + | +++ |
Benchtop stability of assembled reactions | Yes | Yes | Up to 24 hr |
Certified low level of residual DNA |
| N/A |
|
Stand-alone enzyme |
|
| |
Master mix format | Colorless Order now | N/A | Colorless Green* |
Storage temperature | –20°C** | –20°C | –20°C** |
Ambient shipping | Yes | No | No |
*Contains electrophoresis tracking dyes and a density reagent for direct gel loading of PCR products.
**Master mixes can be stored at 4°C for up to 3 months after thawing.
Figure 1. AmpliTaq Gold 360 DNA Polymerase amplifies a broad range of targets. The panel shows products amplified with AmpliTaq Gold 360 DNA Polymerase. PCR was performed in duplicate with 1 ng of template DNA per reaction. Amplicons ranged from 300 to 1,400 base pairs (bp) in length with an average length of 553 bp. Amplicons are labeled as follows: high AT, easy amplification, primer dimer, homopolymer, sequencing challenge, long, high GC. The high GC amplicon reactions included 5 µL of 360 GC Enhancer.
Figure 2. Sensitivity of AmpliTaq Gold 360 DNA Polymerase for detection of low copy targets. A gel image showing the amplification products of the β-actin gene performed with 0 to 80 copies of input DNA, using 2.0 mM MgCl2 and standard thermal cycling conditions.
Figure 3. High-quality sequencing data obtained from AmpliTaq Gold 360 DNA Polymerase-generated PCR products. Amplification products from both standard (A) and high GC content (B) targets generated by AmpliTaq Gold 360 DNA Polymerase and AmpliTaq Gold DNA Polymerase were sequenced (10 ng PCR product per sequencing reaction). Samples were cycle-sequenced using BigDye Terminator v3.1 and standard thermal cycling conditions. BigDye XTerminator Purification Kit was used to clean up the cycle sequencing reaction, and the samples were injected into the Applied Biosystems 3730xl DNA Analyzer with POP-7 polymer.
Figure 1. AmpliTaq Gold 360 DNA Polymerase amplifies a broad range of targets. The panel shows products amplified with AmpliTaq Gold 360 DNA Polymerase. PCR was performed in duplicate with 1 ng of template DNA per reaction. Amplicons ranged from 300 to 1,400 base pairs (bp) in length with an average length of 553 bp. Amplicons are labeled as follows: high AT, easy amplification, primer dimer, homopolymer, sequencing challenge, long, high GC. The high GC amplicon reactions included 5 µL of 360 GC Enhancer.
Figure 2. Sensitivity of AmpliTaq Gold 360 DNA Polymerase for detection of low copy targets. A gel image showing the amplification products of the β-actin gene performed with 0 to 80 copies of input DNA, using 2.0 mM MgCl2 and standard thermal cycling conditions.
Figure 3. High-quality sequencing data obtained from AmpliTaq Gold 360 DNA Polymerase-generated PCR products. Amplification products from both standard (A) and high GC content (B) targets generated by AmpliTaq Gold 360 DNA Polymerase and AmpliTaq Gold DNA Polymerase were sequenced (10 ng PCR product per sequencing reaction). Samples were cycle-sequenced using BigDye Terminator v3.1 and standard thermal cycling conditions. BigDye XTerminator Purification Kit was used to clean up the cycle sequencing reaction, and the samples were injected into the Applied Biosystems 3730xl DNA Analyzer with POP-7 polymer.
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For Research Use Only. Not for use in diagnostic procedures.