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DNA extraction was performed using the conventional bead beater method (Sambrook and Rusell 2006) with modifications.
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Major element concentrations were measured with an X-ray fluorescence spectrometer (XRF: MagiX PRO, Spectris) using the conventional glass bead method.
Major element concentrations were determined by an X-ray fluorescence spectrometer (XRF; MagiX PRO, Spectris, Egham, Surrey, UK) installed at the Kochi Core Center (KCC), Kochi, Japan, using the conventional glass bead method.
Using the conventional S-BUS ports.
This article uses the conventional dating.
Group carbohydrate was determined using the latex bead agglutination test.
Microarray analysis was conducted using the Illumina Bead Chip.
An antibody-bead array of 35 markers was constructed using the Luminex™ bead array platform.
Templated bead preparation was performed using the SOLiD EZ Bead system (Applied Biosystems).
Additional Templated beads were deposited on slides using the Bead Deposition kit from Applied Biosystems.
Emulsion PCR and bead-based enrichment was carried out using the SOLiD EZ bead system.
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