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Data for animals showing isotope inconsistencies due to contamination by ambient air of blood samples were discarded.
All blood samples were discarded when HIV testing was complete.
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While the cannula was left in place, the cannula was flushed prior and post blood sampling with sodium-citrate solution, and the first 10 ml of blood sampled were discarded.
The first few millilitres of each blood sample was discarded to avoid any possible contamination by normal skin melanocytes.
The first 3 5 ml of each blood sampling was discarded before the sample for analysis was collected in order to avoid contamination of skin epithelial cells.
The first blood sample was discarded, but on June 16 and June 24, additional serum and whole blood samples were collected in sodium citrate vacutainer tubes (Becton-Dickinson, Franklin Lakes, NJ, USA).
Blood-contaminated synovial fluid samples were discarded.
Samples were discarded if the CSF was contaminated with blood >25 RBCs/μl present in the sample.
GCF samples were discarded for further analysis if they were visibly contaminated with blood.
Hemolysed samples were discarded.
All poor quality RNA samples were discarded.
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