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Best results are obtained using high-quality RNA samples for preparation and hybridization.
Blood samples for preparation of EDTA-plasma were placed in ice water, and plasma was separated within 4 h.
They provided finger-prick blood samples for preparation of thick- and thin-blood smears, hemoglobin measurement (HemoCue Ltd., Angelhölm, Sweden), and collection of blood spots on filter paper (Whatman 3MM; Whatman, Maidstone, United Kingdom).
Blood samples for preparation of citrated plasma were drawn immediately before starting the study drug infusion, 4, 8, and 12 hours after the start of the study drug infusion, and once daily on days 2, 3, 4, 5, and 6 of treatment.
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The mixed solutions were used for fortification of samples and for preparation of matrix-matched standards.
The NEXTflex Dual-Indexed DNA Barcodes are designed for multiplexing of up to 192 samples for library preparation.
Tumor samples for RNA preparation were immediately frozen in liquid nitrogen after isolation.
Blood samples for DNA preparation were taken into tubes containing sodium citrate and stored at −20 °C.
We took samples for RNA preparation after 2, 4 and 6 hours from both cultures.
In response, the state shortened the fourth-grade assessment and students were given sample questions for preparation.
The method of sampling and sample preparation for the chemical analysis was according to Indian Standard (IS: 436, 1964).
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