ROTI®Pol Hot-TaqHY, 40 µl, 1 x 40 µl
Transport temp. cooled
Modified HotTaq polymerase in storage buffer, PCR buffer (10x), PCR buffer red (10x)
excl. VAT. | 40 µl per Pack Qty.
Art. No. 9346.1
Fits to / Accessories
For PCR. Recombinant, heat stable DNA polymerases from the thermophilic bacteria Thermus aquaticus.
ROTI®Pol, the series of DNA polymerases is the optimal choice for all PCR cycling protocols, as being performed in, for instance, analysis of cloning efficiency, for gene fishing, in routine screening processes, educational assays and much more. In combination with our specially designed buffers, the ROTI®Pol DNA polymerases deliver specific and reproducible PCR amplification with a wide range of PCR templates.
ROTI®Pol Hot-TaqHY 5 U/μl
Modified version of the recombinant hot start Taq DNA polymerase from the thermophilic bacterium Thermus aquaticus in storage buffer, plus additional 10x concentrated PCR reaction buffer and 10x concentrated PCR reaction buffer with red gel loading dye. ROTI®Pol Hot-TaqHY is recommended for use in highly specific PCR applications with particularly high yields.
This polymerase set ROTI®Pol Hot-TaqHY is superior for all sophisticated Taq-based cycling protocols, in which both, particularly specific amplification as well as very high yields shall be obtained, or if highly specific amplifications shall be performed using particularly short cycle times.
Thus, ROTI®Pol Hot-TaqHY is the perfect choice prior to cloning or sequencing processes, for cycle sequencing and for colony PCR, and it may also well be used in qPCR- and multiplex PCR applications.
Combining the benefits of both techniques, the Hot-TaqHY DNA polymerase has been designed by increasing the PCR sequence specificity of a quick and high yield modified Taq polymerase by antibody mediated inhibition. In combination with our unique buffers, the Hot-TaqHY polymerase delivers highly specific PCR amplification of superior yield with a wide range of PCR templates. The blocked Taq polymerase is getting active only after the initial denaturation step, resulting in highly specific amplification of the target sequence without production of unwanted side products due to unspecific primer annealing. In parallel, the modification of the DNA polymerase results in significantly enhanced amplicon yields, with the benefit of shorter elongation times needed.
ROTI®Pol Hot-TaqHY is able to amplify PCR products up to 3 kb with genomic DNA and up to at least 5 kb in size with Lambda DNA and is appropriate for use in the amplification of DNA from a wide range of even complex templates. The Hot-TaqHY DNA polymerase included in the set possesses a 5’ → 3’ polymerase- as well as a 5’-flap endonuclease activity, and generates a 3’dA (adenine)-overhang which may well be used for TA-cloning purposes.
M: 100 bp-DNA Ladder extended. NTC: no template control.
Filled in colour coded tubes, the set contains the DNA polymerase and two 10x concentrated reaction buffers with 20 mM MgCl2, one of which has been specially designed for direct gel loading following the PCR reaction. In 1 % agarose gels, the included red dye migrates approx. as fast as a 1 kb DNA fragment. During denaturation in Southern blotting, the dye turns yellow at an acidic pH. The use of the colourless PCR reaction buffer is adequate for all general PCR applications and is particularly recommended when direct fluorescence or absorbance readings are required.
Hot-TaqHY polymerase in storage buffer containing 50 % glycerol, PCR buffer (10x) with 20 mM MgCl2, PCR buffer red (10x) with 20 mM MgCl2 and 0,1 % cresol red.
Colour coded tubes.
Contents of this set may not be bought separately.
|Application||Particularly sequence specific, fast PCR protocols and/or high yield, GC rich template DNA|
|Polymerase||High yield / high performance hot start Taq polymerase|
|Reaction buffer||colourless + red (ready to load)|
|Use||Particularly sequence specific, fast PCR protocols and/or high yield, GC rich template DNA|
- Subtotal: 0.00
|Art. No.||Pack Qty.||Pack.||Packaging||Price||Quantity|
|9346.1||40 µl||plastic||1 x 40 µl||
|9346.2||200 µl||plastic||5 x 40 µl||
No longer available
Delivery date currently unknown
- Subtotal: 0.00
Downloads / MSDS
Enzyme: a neoclassical, Greek artificial word ενζυμου, énzymon, derived from εν-, en- (in-) and ζυμη, zýmé (yeast, sourdough, archaic)
Ferments: comes from the Latin fermentum (ferments, sourdough)
There are six classes in which all enzymes are classified according to the particular reaction they catalyse:
• Oxidoreductases (catalyse redox reactions)
• Transferases (transfer functional groups among substrates)
• Hydrolases (cleave bonds via addition of water)
• Lyases/Synthases (cleave or synthesise complex products out of basic substrates without cleavage of ATP)
• Isomerases (transform chemical isomers)
• Ligases/Synthetases (cleave or synthesise complex products out of basic substrates via cleavage of ATP)
Certificates of Analysis
|Purity (enzyme)||≥98 %|
|Enzyme activity||5 U/µl|
|Endonuclease activity||none detected|
|Exonuclease activity||none detected|
|Suitability for PCR (400 bp)||complies|
|Suitability for PCR (3 kb)||complies|
|Suitability for PCR (5 kb)||complies|
|Selective specificity in PCR||complies|
|Hot start functionality||complies|
|Stability (in storage buffer)||complies|