DreamTaq™ DNA Polymerase generates PCR products with 3′-dA overhangs. The enzyme is . software at or follow the general . In certain countries use of this product is covered by patents. Purchase of product in these countries includes non-transferable, limited license for using only this. Thermo Scientific™ DreamTaq DNA Polymerase. Get higher sensitivity, longer PCR products and higher yields in all standard PCR applications with this.

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PCR amplifications were performed using 0. The master mix is supplemented with two tracking dyes and a density reagent that allows for direct loading of the PCR product on a gel. When using a thermal cycler that does not contain a heated lid, overlay the reaction mixture with 25? Excessive primer concentrations increase drdamtaq probability of mispriming and generation of non-specific PCR products.

Annealing for 30 seconds is normally sufficient. The master mix retains all features of DreamTaq? Data for dreamtaq buffer gathered from related PubMed articles.

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Primers The recommended concentration range of the PCR primers is 0. All cDNA samples were run in triplicates and water was used as a negative control. Higher amounts of template increase the risk of generation of non-specific PCR products. The thermal cycles were as follows: For degenerate primers and primers used for long PCR we recommend higher primer concentrations in the range of 0.

Data for dream taq green buffer gathered from related PubMed articles. Number of cycles If less than 10 copies of the template are present in the reaction, about 40 cycles are required. For more information please contact info fermentas. Troubleshooting For troubleshooting please visit www. DNA polymerase, optimized DreamTaq?


General recommendations to lower the risk of contamination are as follows: For higher template amounts, cycles are sufficient. Therefore, care must be taken to avoid contamination with other templates and amplicons that may be present in the laboratory environment.

Fermentas DreamTaq DNA Polymerase, 5 x 500U

Commonly Used Together rdeamtaq green dnadreamtaq polymerasedntpsdntpdeoxynucleoside triphosphatesdmso dntp mixmgcl 2dreamtaqrnase a. If the primer contains more than 25 nucleotides we recommend using specialized computer programs e.

A novel badnavirus discovered from Betula sp. This product is licensed under one or more U. Check for possible sites of undesired complementary between primers and template DNA.

Not stealing from the treasure chest or just a bit: Use positive displacement pipettes, or pipette tips with aerosol filters to prepare DNA samples and drexmtaq PCR set up. Wear fresh gloves for DNA purification and reaction set up. Avoid self-complementary primer regions, complementarities between the primers and direct primer repeats to prevent hairpin formation and primer dimerization.

Gently vortex fermenttas briefly centrifuge DreamTaq? Perform PCR using the recommended thermal cycling conditions outlined below: The effects of amoxicillin treatment of newborn piglets on the prevalence of hernias and abscesses, growth and ampicillin resistance of intestinal coliform bacteria in weaned pigs All E. Lower amounts of template reduce the accuracy of the amplification.

PCR conditions were as given in Additional file.

Analyses on plant derived writing supports and non-invasive DNA sampling Due fermentsa fragmentation, only short amplicons were tested for historic samples. Ten years of life in compost: The gene expression of the neuronal protein, SLC38A9, changes in mouse brain after in vivo starvation and high-fat diet Paragraph title: Ideally, C and G nucleotides should be distributed fermentzs along the primer.


Place a thin-walled PCR tube on ice and add the following components for each 50?

Ordering Information Component DreamTaq? For applications that require PCR product analysis by absorbance or fluorescence excitation, we recommend using the colorless DreamTaq? FPa core-genome gene highly conserved in F.

Green buffer is a proprietary formulation optimized for robust performance in PCR.

Omitting the primers sequences, the amplified fragment was nucleotides long. PCR primers are generally nucleotides long.

In certain countries use of this product is covered by patents. This product is licensed under U. Plant genomes enclose footprints of past infections by giant virus relatives Genomic DNA was isolated from protonemal tissue as previously described. It contains a density reagent and two dyes for monitoring electrophoresis progress: Data for box pcr reaction mix gathered from related PubMed articles.

The primer sequences were published previously Schulte et al. Primer design and quantitative real-time PCR The volume was adjusted with sterile water. The dyes have absorption peaks at nm and nm. Thermo Fisher dreamtaq buffer Bioz Stars score: Thermo Fisher dream taq green buffer Bioz Stars score: