Although the MTS was required, the MTS of this peptide sequence could be replaced with the MTS from mRNAs that are translated on free cytoplasmic ribosomes, such as COX4 or ATP16, without affecting asymmetric mRNA localization.
The MTS "MultiFlex" System precisely controlled the applied loads and displacements through the actuators.
The MTs exploit the SR communication capabilities to reach the LR AP consuming less energy.
The MTS assay was performed and the cell viability was determined.
The MTs polymorphism pattern is essentially the same for the 12 Drosophila species.
The MTS assay was used to determine the cytotoxicity of compounds in gastrointestinal cancer cells.
The MTS will use a 1-MW proton beam to generate neutrons through spallation reactions.
The MTS assay was carried out after 5 days of culture.
The MTs can be further stabilized by MT-associated proteins (MAPs) and tau which bind along the MTs to decrease depolymerization.
The MTS assay (Promega, Madison, WI) was then conducted according to the manufacturer's protocol.
The MTS cell proliferation assay was purchased from Promega.
