HotStarTaq DNA Polymerase (25000)

PCR Hot start PCR - Bacterial DNA

Experiment
PCR Hot start PCR - Bacterial DNA
Product
HotStarTaq DNA Polymerase (25000) from Qiagen
Manufacturer
Qiagen

Protocol tips

Publication protocol

PCR amplification and Nanopore library construction and sequencing: Primer sets 16S27F/16SR1495 (5’-AGAGTTTGATCMTGGCTCAG-3’ / 5’- TACGGYTAC CTTGTTACGACTT-3’) [34] and Cn_pPer11F/Cn_pPer986R (5’-CCTCGACCACCGCC GCGA-3’ / 5’-CGGCTCCTGCCCCTCGGG-3’) fused to Nanopore-specific oligonucleo- tides were used for 16S rRNA and purine permease amplifications, respectively. PCR amplifica- tions of all replicates of the mock bacterial communities (Cn-spiked or not) and corn leaf samples (diseased and healthy) were performed using HotStar Taq Plus DNA polymerase kit (Qiagen, Canada) and barcoded using the SQK-PBK004 PCR Rapid Barcoding kit (ONT) targeting 16S rRNA and purine permease genes where required. Briefly, a PCR reaction (total volume of 60 μl) consisted of 6 μl QIAGen HotStar 10x Buffer, 12 μl 5x Q-sol, 0.75 μl of 2.5 mM dNTPs, 0.6 μl 20 nM of each primer, 1.8 μl of LWB Barcodes (ONT), 0.6 μl of Taq polymerase plus (5U/μl; Qiagen), 6 μl DNA template (5 ng/μl), and 21.65 μl of PCR H2O. PCR parameters performed in a TProfe- sional thermocycler (Biometra, Germany) were an initial denaturation at 95 ̊C, 5 min; followed by 40 cyles of 95 ̊C, 30 sec, 65 ̊C, 30 sec, 72 ̊C, 60 sec; and a final extension at 72 ̊C, 5 min. For quality control, 3 μl of the PCR amplicons were verified by agarose (1.3%) gel electrophoresis. The remaining 57 μl of PCR products were purified by Amicon Ultra-0.5 Centrifugal Filters (Milli- pore, Canada). The DNA concentration of the purified PCR products were quantified by Qubit High Sensitivity DNA assay (ThermoFisher, Canada) as recommended by the manufacturer.

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Discussion

Discussion

4 years ago

Author: Qatar

When should I add the polymerase for hot start PCR?

I keep getting a non-specific band in PCR so I would like to try a hot start PCR manually. How should I prepare the mix and at which step should I be adding the polymerase?

Discussion

4 years ago

Author: Janina Reinhardt Switzerland

Hot start PCR using phusion green DNA polymerase

I am currently performing hot start PCR using phusion green hot start DNA polymerase in order to amplify a 8.8kb insert. However, I cannot get any amplified product at all. I have tried changing some parameters but I am not sure what to do. Any help?

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Papers

Check out relevant papers found by Labettor's AI that are relevant for performing PCR Hot start PCR - Bacterial DNA using HotStarTaq DNA Polymerase (25000) from Qiagen.

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Manufacturer protocol

Download the product protocol from Qiagen for HotStarTaq DNA Polymerase (25000) below.

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