Jump to content Jump to navigation menu

ROTI®Pol Hot-TaqS, 40 µl, 1 x 40 µl

5 U/μl
Icon_Eisstern All products identified as being particularly temperaturesensitive are shipped in special ice boxes with freezer packs or in dry ice.
Pack Qty.
DNA polymerase (thermostable), Hot start DNA polymerase, Taq DNA polymerase, recombinant, Polymerase (thermostable)
Storage temp. -20 °C
Transport temp. cooled

For particularly sequence-specific PCR amplifications.
HotTaqS polymerase in storage buffer, PCR buffer (10x), PCR buffer red (10x)

For PCR. Recombinant, heat stable DNA polymerases from the thermophilic bacteria Thermus aquaticus.
Product details

€79.05/Pack Qty. 

excl. VAT. | 40 µl per Pack Qty.

Art. No. 9245.1

In stock
Delivery fast, simple and reliable!
from 6 Pack Qty. €75.10/Pack Qty.
from 24 Pack Qty. €71.14/Pack Qty.

Product details

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-TaqS 5 U/μl

Hot start version of the recombinant heat stable 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-TaqS is recommended for use in highly specific PCR applications.

This polymerase set ROTI®Pol Hot-TaqS is outstandingly suitable for all Taq-based cycling protocols, in which particularly specific amplification is the main focus - as being performed in, for instance, prior to cloning or sequencing processes, in cycle sequencing, and in similar assays. In combination with our unique buffers, the Hot-TaqS polymerase delivers highly specific PCR amplification of good yield with a wide range of PCR templates. The antibody-mediated blocking of the DNA polymerase is released only at the initial denaturation step, hence resulting in highly specific amplification of the target sequence without production of unwanted side products caused by unspecific primer annealing.

ROTI®Pol Hot-TaqS 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 genomic, viral, and plasmid templates. The Hot-TaqS 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.

Figure: Sensitivity assay using ROTI®Pol TaqS, TaqHY, Hot-TaqS and Hot-TaqHY, 1 U/reaction each (20 μl). 300 bp β-Actin fragment, 40 cycles. Template: 10 to 2000 pg human gDNA. Gel loading 10 μl each.
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.

The set contains

Hot-TaqS polymerase in storage buffer containing 50 % glycerol, PCR buffer (10x) incl. 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.

Not a medical device / Not an IVD product
Technical Information
Application Particularly sequence specific standard PCR 
Amplicon ends 3'dA 
Polymerase Hot start Taq polymerase 
Reaction buffer colourless + red (ready to load) 
Use Particularly sequence specific standard PCR 
ROTI®Pol Hot-TaqS
Selected quantity:   0
  1. Subtotal:  0.00
Art. No. Pack Qty. Pack. Packaging Price Quantity
9245.1 40 µl plastic 1 x 40 µl


9245.2 200 µl plastic 5 x 40 µl


In stock
In procurement
No longer available
Delivery date currently unknown
Selected quantity:   0
  1. Subtotal:  0.00

Downloads / MSDS

General information

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

You can search for and download your certificate of analysis for the selected product here. Please provide your batch number.
The following analysis certificates have been found:

Type analysis

Purity (enzyme)≥98 %
Enzyme activity5 U/µl
Endonuclease activitynone detected
Exonuclease activitynone detected
Suitability for PCR (400 bp)complies
Suitability for PCR (3 kb)complies
Suitability for PCR (5 kb)complies
Selective specificity in PCRcomplies
Hot start functionalitycomplies
Stability (in storage buffer)complies