DTI FabTaq HS-Glycerol Free (50U/ul)
PCR Polymerase Enzyme

DTI FabTaq HS-Glycerol Free (50U/ul)

DTI FabTaq HS-Glycerol Free (50 U/ul) is a hot start PCR enzyme derived from Thermus aquaticus that includes a neutralizing monoclonal antibody that recognizes Taq DNA polymerase. This antibody binds to Taq DNA polymerase and prevents non-specific amplification due to mispriming and/or formation of primer dimers before thermal cycling. The antibody is denatured during the initial DNA-denaturation step, allowing this product to be used with standard PCR conditions. Since the product is glycerol free, it is suitable for lyophilization processes.

Catalog & Pack Sizes
DT0103.2500 2500 U

Specifications

  • Storage and Shipment Conditions: -80°C
  • Unit Definition: One unit is the amount of enzyme that will incorporate 10 nmol of dNTPs into acid-insoluble products in 30 minutes at 74°C with activated salmon sperm DNA as the template-primer.
  • Application:
    For DNA amplification by hot start PCR
    For DNA sequencing
    For further manufacturing and lyophilization processes.
  • Purity: Nicking, endonuclease, and exonuclease activity were not detected after incubation of 0.6 μg of supercoiled pBR322 DNA, 0.6 μg of λDNA, or 0.6 μg of λ-Hin d III digest with 10 U of this enzyme for 1 hour at 74°C.
  • Quality Control Data: Please see the certificate of analysis for each lot.

Documents & Downloads

Download product manuals, certificates, and technical resources below.

PDF

DTI FabTaq HS-Glycerol Free (50U/ul) - Protocol

Instructions for use and step-by-step protocol.

Download User Manual
PDF

DTI FabTaq HS-Glycerol Free (50U/ul) - Certificate of Analysis

Batch-specific quality control results.

Download CoA (DT0103.2500)

Experimental Sample

a) Amplification data: Good performance of this product has been confirmed by PCR using λ DNA as template (amplified fragment size 8 kbp). The protocol used for the assay and the results are as follows:

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Figure 1: Amplification data showing product performance with λ DNA as template.

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Figure 2: Amplification data for λ DNA (8 kbp amplified fragment size).

b) Hot start function data: Test target sample added to a PCR system containing FabTaq and FabTaq HS respectively. Following an incubation at RT for 30 mins, the products were amplified using a thermal cycler. Non-specific bands (around 280 bp) were observed in the PCR system along with specific target bands (838 bp) using FabTaq, while there were no non-specific bands observed in PCR system using FabTaq HS.

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Figure 3: Additional data showcasing product performance.

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Figure 4: Hot start function data showing non-specific bands in PCR system with FabTaq and absence of non-specific bands with FabTaq HS.