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It is only after these protective matrices were removed by treatment with HCl and HF that these compounds became evident.
After composite resin polymerization using a halogen light apparatus (VIP, Bisco, Schaumburg, USA/550 mW/cm2 for 20 seconds), the matrices were removed and the specimens stored in distilled water at 37°C for 24 h.
Outliers identified by hierarchical clustering and/or dissimilarity matrices were removed.
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For purposes of performance evaluation, the scaling ambiguities affecting the estimates of the channel matrices are removed by assuming the first column of Hsr and first row of Hrd contain all one elements, similarly to [11, 14].
Non-invading cells on top of the matrix were removed by rubbing with a moistened cotton swab.
Highly inter-correlated variables with statistically significant correlation coefficient greater than 0.9 in the correlation matrix were removed from the model.
Here, zero rows in the regression matrix were removed, and the rows and columns of T d 's have been reordered by the co-clustering procedure.
The cells were allowed to invade for 24 hours, after which, the noninvading cells with Matrigel matrix were removed from the upper surface of the membrane by scrubbing with a cotton-tipped swab.
The PMMA matrix was removed by exposure to UV radiation.
In this case the polymer matrix was removed by plasma treatment.
The extracellular matrix is removed by enzymatic digestion, and the cells are then expanded in monolayer culture.
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