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Six healthy subjects were chosen to collect the blood sample for separation of lymphocytes and collection of squamous epithelial cell by scraping.
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Blood samples for serum separation were collected from the jugular vein of apparently healthy camels using labeled plain vacutainer tubes following proper physical restraining.
Blood samples for the separation of plasma for M30 and M65 ELISA analyses were collected from all eligible subjects entered into the Cancer Research UK-sponsored phase I Trial of OXi4503, where the drug was administered by 3 × weekly intravenous infusions to patients with advanced solid tumours (CR-UK Protocol Number: PH1/098 and Eudra CT Number: 2004-002375).
All studies used blood sample for genotyping.
The blood samples for CRP analysis were collected in serum separation tubes, and the serum CRP levels were measured via immunoturbidimetry (Denka Seiken Co. Ltd., Japan).
The blood samples for flow cytometry analysis were treated in 5 hours; serum separation was completed within 24 hours.
Blood samples for biochemical and hormonal determinations were collected in tubes for serum separation.
This paper concerns the development of membranes for the separation of highly deformable red blood cells from whole blood samples, for use in biosensor assemblies.
Furthermore, peripheral blood mononuclear cell (PBMC) were isolated from the first whole blood sample by density separation over Ficoll-Hypaque.
Multi-decay power pulses through a blood sample to determine separation efficiency that provides accurate attenuation measurements.
To determine CRP blood samples were centrifuged for separation of the serum within 60 minutes of blood collection and analysis was performed using COBRA 400/400 plus system (Roche Diagnostic limited, Switzerland).
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