|Related Categories||Application Index, Biochemicals and Reagents, Core Bioreagents, Enzymes, Inhibitors, and Substrates, General Reagents,|
Includes 10× PCR reaction buffer without MgCl2 and a separate tube of 25 mM MgCl2
• Enhanced amplification on genomic and difficult DNA templates
• Same great performance as Taq DNA Polymerase in a more convenient format for high throughput applications
• Quick recognition and confirmation of appropriate mixing
• No loading buffers or tracking dyes necessary. Sample can be taken directly from reaction and loaded onto an agarose gel
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.
REDTaq is a registered trademark of Sigma-Aldrich Co. LLC
One unit incorporates 10 nmol of total dNTPs into acid precipitable DNA in 30 min. at 74°C.
REDTaq Genomic DNA Polymerase is a unique blend of Taq DNA Polymerase with an inert red dye. This special formulation is designed to provide enhanced amplification of more complex or genomic templates. REDTaq Genomic DNA Polymerase is highly sensitive, produces increased yields and is capable of generating longer product lengths. It has all the advantages of REDTaq DNA polymerase, such as easy visualization of enzyme addition and complete reaction mixing, and direct loading to an agarose gel. The dye migrates slightly faster than bromophenol blue at approximately the same rate as a 125 base pair fragment.
The inert red dye does not effect automated or manual sequencing, restriction digestions or other downstream applications. The dye can easily removed by any standard purification method.
Customers Also Viewed
Hot-start high fidelity Taq enzyme with inert dye, 10X buffer included
Taq for routine PCR with inert dye, 10X buffer included
Complete PCR reagent with standard Taq DNA Polymerase and inert dye
with 10× PCR reaction buffer containing MgCl2, recombinant, expressed in E. coli
Certificate of Analysis
Innis, M.A., et al. PCR Protocols: A Guide to Methods and Applications, (1990)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Need larger quantities for your development, manufacturing or research applications?