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Gastric tissue obtained at necropsy (n = 28 monkeys) and frozen at −80C for between 1 week and 22 months (median 13.8 months), was shipped to U.C. Davis, fixed, and processed in the laboratory of J. Solnick for H. pylori culture and histopathology respectively as previously described [15].
The GC-TOF-MS based metabolite profiles were performed and processed in the laboratory of JK.
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Samples were processed in the laboratory on the day of collection.
Clinical material collected from the case-patients and their contacts was initially processed in the laboratories of these hospitals.
Blood samples were taken by jugular venipuncture using a potassium-EDTA vacutainer (BD Vacutainer Systems, Plymouth, UK) and stored at 4°C before being processed in the laboratory within 72h of collection.
Stool samples were processed in the laboratory within 2 h of collection for the isolation of V. cholerae.
All samples were processed in the laboratory within 20 minutes of the bronchoscopy.
The ovaries were clamped together pair-wise with an ID-tag, pooled in 0.9% NaCl solution at 38 C and processed in the laboratory within 3.5 - 4 h of collection.
However, following the completion of these studies, the number of CSF samples processed in the laboratory has remained static.
All faecal samples collected were processed in the laboratory by the author within 24 hours of sample collection.
We selected a total of 160 yeast-positive blood culture bottles among 405 bottles of the BACTEC system yielding yeasts that were sequentially processed in the clinical laboratory of the Hospital São Paulo, Universidade Federal de São Paulo, between October 2008 and February 2012.
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