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Magmax cell free dna extraction kit

Manufactured by Thermo Fisher Scientific
Sourced in United States

The MagMax Cell Free DNA extraction kit is a lab equipment product designed for the isolation and purification of cell-free DNA (cfDNA) from various sample types. It utilizes magnetic bead-based technology to efficiently capture and extract cfDNA, providing a reliable and consistent method for obtaining this analyte.

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4 protocols using magmax cell free dna extraction kit

1

Urothelial Bladder Cancer DNA Analysis

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We studied 19 patients who were diagnosed with urothelial BC who received TURBT (13 NMIBC and six MIBC; 18 males; and 3 females). Informed consent was obtained from all patients. This study was approved by the Institutional Review Board of clinical research and genome research committee at Yamanashi Central Hospital (G-2018-1) and complied with Declaration of Helsinki principles. Peripheral blood samples were obtained and centrifuged to separate buffy coats (12 (link)). Urine was also centrifuged and separate into urine precipitate and supernatant. Buffy coat, urine precipitate, and urine supernatants were stored at −80°C until DNA extraction. Buffy coat was used as a control to detect somatic mutations in tumor tissues. DNA from buffy coat and urine precipitate was extracted with the QIAamp DNA Blood Mini QIAcube Kit (Qiagen, Hilden, Germany) and the DNA concentration was determined using a Nano Drop 2000 (Thermo Fisher Scientific, Waltham, MA, United States). DNA was extracted from the urine supernatant with the MagMax Cell Free DNA extraction kit and KingFisher Duo Prime (Thermo Fisher Scientific). DNA from urine supernatant was determined using the Qubit dsDNA HS Assay Kit and Qubit 3.0 fluorometer (Thermo Fisher Scientific) according to the manufacturer’s instructions.
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2

Urine and Blood DNA Extraction

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This study included 25 patients who were diagnosed with BC by transurethral resection of bladder tumor (TURBT), four patients with cystitis and one patient with inverted papilloma (25 males and 5 females; age 50‐90 years) (Table S1). Informed consent was obtained from all patients. This study was approved by the Institutional Review Board at Yamanashi Central Hospital. Urine and blood samples were obtained before TURBT. Urine precipitate (cellular fraction) and urine supernatant (non‐cellular fraction) were collected after centrifugation (Figure 1).18DNA was extracted from the buffy coat and urine precipitation with the QIAamp DNA Blood Mini QIAcube Kit (Qiagen, Hilden, Germany) and DNA concentration was determined using Nano Drop 2000 (Thermo Fisher Scientific, Waltham, MA, USA). DNA was extracted from the urine supernatant and plasma with the MagMax Cell Free DNA extraction kit and the KingFisher Duo Prime (Thermo Fisher Scientific).
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3

Cell-free DNA Isolation from Liquid Biopsy

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Isolation of cell-free DNA was performed using the bead-based MagMAX™ Cell-free DNA extraction kit (catalog no.: A36716, Thermo Fisher Scientific, Waltham, MA, USA), specialized for high-quality isolation and specific enrichment of nucleic acids from liquid biopsies, as previously reported [11 (link)].
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4

DNA Extraction from Blood and Tumor Samples

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Peripheral blood samples were collected and centrifuged to separate buffy coats and plasma. Buffy coats were stored at − 80 °C until DNA extraction. Buffy coat DNA was extracted with the QIAamp DNA Blood Mini QIAcube Kit (Qiagen, Hilden, Germany). The DNA concentration of buffy coats was determined using a NanoDrop 2000 (Thermo Fisher Scientific, Waltham, MA, USA). Plasma DNA was extracted with the MagMax Cell-Free DNA extraction kit on the KingFisher Duo Prime (Thermo Fisher Scientific). Concentration of plasma DNA was determined using the Qubit dsDNA HS Assay Kit and Qubit 3.0 fluorometer (Thermo Fisher Scientific) according to the manufacturer’s instructions.
Tumor tissues were fixed using 10% buffered formalin29 (link). Serial 10 μm sections were prepared from formalin-fixed paraffin-embedded (FFPE) tissues, and sections were stained with hematoxylin–eosin and reviewed by a pathologist to check the tumor area. Laser capture microdissection was performed using an Arcturus XT laser microdissection system (Thermo Fisher Scientific). FFPE DNA was extracted using the QIAamp DNA FFPE Tissue Kit (Qiagen), the GeneRead DNA FFPE Kit (Qiagen), and the MagMAX™ FFPE DNA/RNA Ultra Kit (Thermo Fisher Scientific) according to the manufacturer’s instructions. FFPE DNA concentrations were determined using the Qubit® dsDNA HS Assay Kit on a Qubit Fluorometer 3.0 (Thermo Fisher Scientific).
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