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New types of nanogold labels were evaluated for their improved sensitivity in procalcitonin lateral flow immunoassay (LFIA).
For documents with multiple subtype labels, the labels were evaluated separately.
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Stromal and myometrial labelling were evaluated independently for ER-α and PR in both normal and neoplastic epithelium.
The labeling was evaluated in a Leica DM5000 fluorescent microscope and pseudocolor images were acquired for analysis.
In vivo plaque labeling was evaluated in a transgenic mouse model (Tg2576) engineered to produce excess amyloid plaques in the brain.
Reciprocal labeling was evaluated to determine the internal consistency of quantified proteome changes from Escherichia coli grown under aerobic and anaerobic conditions.
The statistical significance of the results expressed as rates of cells showing prevailing cytoplasmic or cortical CaSR labeling was evaluated by the Chi-square test with the Yates correction for continuity.
The immunohistochemical labeling was evaluated as previously described [ 28].
The IHC-labeling was evaluated on the photographs by two persons.
Semiquantitative scoring of the immunohistochemical labeling was evaluated by a pathologist (S.E.C).
The intensity of labelling was evaluated using a semiquantitative method as described above.
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