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Peripheral blood mononuclear cells (PBMCs) were isolated, and ASCs were enumerated using an ELISPOT assay.
Cells were enumerated using an epifluorescent microscope and digital camera to determine the number of cells captured on the surfaces.
The cells were enumerated using an epifluorescence microscope (Nikon 80I) at 1000×.
Conidia were harvested from AF13 cultures after 7 days of growth, dispensed into sterile water, enumerated using an Orbeco Hellige TB300 IR Turbidimeter (Orbeco Hellige Inc., Sarasota, FL), diluted to 1.5 × 10−7 conidia mL−1, and used on the same day to inoculate maize for aflatoxin production.
Axon encounters were enumerated using an algorithm implemented in c++.
SFU were enumerated using an automated AID ELISpot reader (AutoImmun Diagnostika, Germany).
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All possible design solutions are enumerated using a multi-core supercomputer.
The effluent was collected and the surviving bacteria cells were enumerated using a modified 'Most Probable Number' method.
Cells were enumerated using a Leica fluorescent microscope (DM4000B, Germany).
Furthermore, if the EAs used for mobile pastoralists were enumerated using a different methodology and have a different classification, then it is very easy to exclude them altogether from the sampling frame of any particular survey (see Table 2).
EPCs were enumerated using a standardized flow cytometric protocol.
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