The aim of this study was to investigate morphology and quantify cortical thickness of the cervical isthmus by using Multi-detector Computerized Tomography (MD-CT) scan.
Megakaryocytes were positively identified based on size, morphology, or ploidy and quantified using ImageJ.
Neurons were plated, and cellular morphology was recorded and quantified every 3 h for 48 h using an IncuCyte live-cell imaging system (Essen Instruments, Ann Arbor, MI) located within the incubator.
To examine the impact of MLL4 kncokdown on cell viability, we transfected different types of cultured human cells with MLL4 antisense and examined their morphology under microscope and quantified the cell viability using MTT assay.
In addition, the surface morphologies were investigated and quantified by the surface parameters in terms of RMS roughness (R q) and surface area ratio (SAR).
SEM was used to evaluate changes to morphology and alterations quantified using a customary scale adapted from the H-score method and represented as a percentage.
Fluorescence intensity can be measured using two photon excitation to provide optically sectioned images with sub-cellular resolution and allow tissue morphology to be studied and quantified in detail [ 1– 3].
Colonies were air-dried and quantified by morphology and cytokeratin expression as described [ 16].
The frequency of sporophytic and embryonic lethals, leaf or root mutations, auxotrophic gametophytic mutations as well as numerous phenotypic alterations of gametophyte morphology can be routinely detected and quantified.
Micro-Raman spectroscopy is used to access information on the exact iron oxide phase produced, and high resolution SEM and electron dispersion spectroscopy (EDS) are used to assess the oxide morphology and further quantify the oxide state, including spatial distributions.
