Exact(41)
Cell diameter was measured in the H&E-stained sections of three individual samples in each group using Image J. Immunohistochemical staining was applied to paraffin sections of rat retroperitoneal WAT to examine expression of PGC-1 α and UCP1.
Notice that no staining was applied.
Coomassie brilliant blue staining was applied to confirm the presence of FN on the scaffold surface.
Immunohistochemical staining was applied to brain sections of the control and treated mice to examine the degree of degeneration.
To analyze the division history of HSPCs, CFSE staining was applied to freshly isolated CD34+ cells and flow cytometry was used to detect HSPC generations either in 5 days ECM- or PCD-cultures.
CD45 IF staining was applied to distinguish hematopoietic vs non-hematopoietic cells.
Similar(19)
Oil Red O staining and F-actin staining were applied to assess the change of cell morphologies under adipogenic and osteogenic differentiation, respectively.
Echocardiography, multimodality nuclear medical imaging, and histology staining were applied for the evaluation of infarction.
Perl's Prussian blue staining is applied for displaying ferric iron and ferritin protein.
Furthermore, multimodality clinical imaging and histology staining were applied to evaluate the efficacy of the method compared with traditional modeling by interventional technology.
The combination evaluating methods of echocardiography, single photon emission computed tomography/computed tomography (SPECT/CT), and histology staining were applied to compare the infarct size in three groups.
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