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The probed data from its upstream neighbor nodes share the buffer of the sensor node.
The probed bands were visualized using the AP substrate BCIP/NBT.
The probed arrays were scanned at 570 nm using a confocal laser scanner (Hewlett-Packard G2500A).
The probed and washed filter was imaged on a Storm 860 phosphoimager (Molecular Dynamics, Sunnyvale, CA).
The probed proteins were detected by enhanced chemiluminescent reagents (Thermo).
The probed membrane was then washed and exposed to radiographic film.
The probed blot was processed in a phosphorimager (Storm; GE Healthcare).
The probed nylon membranes were washed and exposed to radiographic film (Life Technologies).
The quantification model used in the data analysis assumed that the probed sample volume within the probe depth was homogeneous in composition.
At the end of each trial, one of the tracked targets was probed and observers were asked to identify the probed target from the presented targets.
The actual nucleotidic similarities between probes and known sequences of marker genes of the probed strain were computed using BlastN.
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