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3 protocols using pyromark gold 96 reagent kit

1

Quantifying CpG site methylation via Pyrosequencing

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PCR products (20 μl) were added to a mix comprising Streptavidin Sepharose HP™ (3 μl; GE Healthcare, Dornstadt, Germany) and binding buffer (37 μl; Qiagen, Hilden, Germany). The contents were mixed at 2000g (Centrifuge 5810R, Eppendorf, Hamburg, Germany) for 10 min at room temperature. Using the Vacuum Prep Tool™ (Qiagen), according to the manufacturer's instructions, single-stranded PCR products were prepared. Sepharose beads with attached single-stranded templates were released into a PSQ 96 Plate Low™ (Qiagen) containing a mix of 40 μl annealing buffer (Qiagen) and the corresponding sequencing primer at 400 nmol l−1 (Supplementary Table 1). Pyrosequencing™ reactions were performed in a PyroMark ID System (Qiagen), according to the manufacturer's instructions, using the PyroMark Gold 96 Reagent Kit (Qiagen). CpG site quantification was performed using Pyro Q-CpG™ methylation software (Qiagen).
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2

Epigenetic Analysis by Bisulfite Pyrosequencing

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An epigenetic analysis was performed by bisulfite pyrosequencing, which is a sensitive and accurate method for the detection of methylation. DNA was treated with sodium bisulfite using the EpiTect Bisulfite Kit (Qiagen), which was followed by the cleanup of bisulfite-converted DNA. PCR amplification was then performed with a PyroMark CpG Assay Kit (Qiagen) and a PyroMark Gold Q96 Reagent Kit (Qiagen) in a PyroMark Q96 system (Biotage AB, Uppsala Sweden). PyroMark PCR master mix includes HotStarTaq DNA polymerase and optimized PyroMark reaction buffer that contains 3 mM MgCl2 and dNTPs, 10x CoralLoad Concentrate, 5x Q-Solution, 25 mM MgCl2, and RNase-free water. The PCR amplicon covers the sequence of human chomosome 3q: NC_000003.12 (179148114.179240084). Nine CpG sites are located in the promoter region of the PIK3CA gene (-100 bps) as indicated with the bold letter ‘C’ and recorded as CpG1-9 (Figure 6A). Finally, the methylation levels of these CpG sites were detected with a PyroMark Gold 96 Reagent Kit (Qiagen) and a PyroMark Q96 ID pyrosequencing system (Biotage). The unmethylated and unconverted DNA samples (Qiagen) were used to control the conversion efficiency during the bisulfite treatment and the accuracy of the methylation analyses. PyroQ-CpG software (Biotage) was used for methylation data analysis.
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3

Bisulfite Pyrosequencing for Epigenetic Analysis

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Epigenetic analysis was performed by bisulfite pyrosequencing, which is a sensitive and accurate protocol [34 (link),35 (link)]. DNA was treated with sodium bisulfite using EpiTect Bisulfite kit (Qiagen) and cleanup of bisulfite-converted DNA was done. PCR amplification was then carried out using PyroMark CpG assay (Qiagen) and PyroMark Gold Q96 Reagent kits (Qiagen) in a PyroMark Q96 system (Biotage AB, Uppsala Sweden). PyroMark PCR master mix includes HotStarTaq DNA polymerase and optimized PyroMark reaction buffer containing 3 mM MgCl2 and dNTPs, 10x CoralLoad Concentrate, 5x Q-Solution, 25 mM MgCl2, and RNase-free water. The PCR amplicon covers the sequence in human chromosome 8: 117962434 to 117962479 (version 37.56). There are four CpG sites in the SLC30A8 gene promoter region as indicated with the bold letter ‘C’ and recorded as CpG1-4 (Figure 1). Finally, methylation levels of these CpG sites were detected by using the PyroMark Gold 96 Reagent kit (Qiagen) and a PyroMark Q96 ID pyrosequencing system (Biotage). The unmethylated and unconverted DNA samples (Qiagen) were used for control of conversion efficiency in bisulfite treatment and accuracy in methylation analyses. PyroQ-CpG software (Biotage) was used for methylation data analysis.
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