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These modern methods have allowed the identification of more cell types than could be visualized by classical histology, particularly in the brain, the immune system, and among the hormone-secreting cells of the endocrine system.
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Matrices of IBS distance (1-IBS) and FST were visualized by classical multidimensional scaling (MDS) in R. The proportion of variance explained by each MDS dimension was calculated as the ratio of the respective eigenvalue to the sum of all eigenvalues [33].
The modules were visualized by classical multidimensional scaling in three dimensions.
SG were visualized by immunofluorescence through the co-localization of the classical SG markers G3BP1 and TIAR [ 33, 34].
To evaluate application of chemically synthesized HA-tagged UbVME 1, EL4 cell lysate was incubated with either the classical HA-tagged probe (prepared by intein chemistry) or synthetic probe 1, and DUB activity was visualized by immunoblotting.
Morphology was visualized by scanning electron microscopy.
Both particles were visualized by TEM.
Polymer remnants were visualized by polarization microscopy.
Cell nuclei were visualized by DAPI staining.
Nanoparticles were visualized by negative staining microscopy.
Protein bands were visualized by ECL.
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