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Diameters of CA and IN.mEos clusters were measured using images from 3-color PALM/dSTORM analysis.
Pitches of the half helices of the first immediate neighbor on each side of cofilin clusters were measured.
For co-localization analysis, juxtaposed (within 1 pixel distance) and overlapping clusters were measured as co-localized.
After 10 days, the diameters of developed cell clusters were measured, and cell clusters with a diameter >100 μm were counted as spheres.
The mean values of the 16 parameters of all investigated carcinomas of the clusters were measured and the ratios of resistant/sensitive clusters determined (Table 3-wrap>).
Although the chelation shifts are typically expected to be larger for the ferrocene-bridged bisphosphine ligand dppf than for the corresponding dppm complexes, 19 the observed Δ δ values are 97.2 ppm for 1 and 85.4 ppm for 2. The FTIR spectra of the triiron clusters were measured both in solution and in the solid phase.
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In contrast, none of the gene lists in the TRANSBIG gene set were predictive after ER-α adjustment, suggesting that none of the significant gene clusters were measuring significantly more information than ER-α gene expression.
The hydrogen storage capacity of ordered porous carbon containing Pd clusters was measured.
The thickness of the sheet itself, ignoring particulate or other clusters, was measured to be about 200 nm.
The current of growth of silver clusters is measured and the data are interpreted on the basis of the theory of progressive nucleation.
The magnetization of the clusters was measured by using vibration sample magnetometer (VSM) as a function of applied magnetic field (Figure 1C).
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