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Each blood sample is assayed for length polymorphism at 6 independent short tandem (STR) repeat loci.
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The hemolyzed blood sample was assayed for the percentage of HbA1c using a ColumnMate analyzer (Helena Laboratories, Beaumont, TX).
Because ATP is released from the formed elements of the blood, plasma from each blood sample was assayed using the methods of Cripps [ 32] for plasma haemoglobin concentration.
A limitation of this study is that only a single blood sample was assayed per participant, however it has been shown that a single measure provides substantial information in postmenopausal women for E1, E2 and SHBG [ 45].
Blood samples were assayed for NEFA and BHBA concentrations.
Fasting blood samples were assayed for putative biochemical risk factors and urine samples for microalbuminuria.
The blood samples were assayed using two commercial RDTs based on immunochromatographic assays: (i) the OptiMAL-IT, designed to detect parasite lactate dehydrogenase (pLDH) of both P. falciparum and other plasmodia, and (ii) the Entebe Malaria Cassette (MC), designed to detect P. falciparum-specific histidine-rich protein 2 (PfHRP2) and P. vivax-specific pLDH.
Blood samples were assayed for hemoglobin and A1C.
Blood samples were assayed for SCr, and urine samples were assayed for uNGAL and KIM-1.
This association was not evident when blood samples were assayed using the LAL.
Blood samples were assayed for both oestradiol (E2) and progesterone (P).
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