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Blood samples were divided into four groups: control untreated (0% haemolysis), positive control treated with 3% hydrogen peroxide (100% haemolysis), 4 μg/ml cisplatin [1] and 2.6 μg/ml NP-Pt hydrocolloid diluted in PBS.
The venous blood samples were divided into portions.
Blood samples were divided into plasma and buffy layers and preserved at −80°C until analysis.
Blood samples were divided equally for whole blood analyses and centrifugation to obtain plasma.
Culture-positive blood samples were divided into two groups, Gram-positive (GP) sample group and Gram-negative (GN) sample group, according to the bacterial species detected.
Citrated blood samples were divided into four groups: a control with no NAC, and three treatment groups (10, 30 and 100 μmol/l NAC).
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Each blood sample was divided in 4 fractions in sterile 2 ml tubes.
To examine technical variation due only to RNA isolation, a single blood sample was divided into four, RNA was separately isolated from each sample and, gene expression was quantified.
Each whole blood sample was divided into two aliquots: whole blood alone; and whole blood + 0.2 mg/ml opsonized zymosan.
Season of blood sampling was divided into autumn winter (April to September) and spring–summer (October to March).
A 10 mL blood sample was divided evenly into anaerobic and aerobic culture bottles at the bedside.
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blood DCs were divided
blood samples were taken
blood samples were collected
blood samples were drawn
blood samples were covered
blood donors were divided
blood vessels were divided
blood samples were performed
blood samples was divided
blood samples were analysed
blood samples were obtained
blood samples were assessed
blood samples were assayed
blood samples were analyzed
blood samples were kept
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