Next, we analyzed the expression profile of miR-208b and miR-499 during differentiation of primary muscle cells (Fig. 5C).
We analyzed the expression profile of cells transfected with a plasmid coding for the intracellular protein EGFP using FuGENE 6 Transfection Reagent only.
To investigate whether the transfection reagent causes side effects, we compared gene expression (using human GeneChip HG U133 Plus 2.0) after transfection of HEK 293 cells with either the FuGENE 6 Transfection Reagent or reagent A. We analyzed the expression profile of cells transfected with a plasmid without insert (pM1-MT) compared with one coding for the secreted protein SEAP (pM1-SEAP).
To determine whether EMT occurs in adult liver cells, we analyzed the expression profile of primary HSC, two HSC lines, and hepatic epithelial progenitors.
To compare with the published transcriptomic study on carbon starvation, we specially analyzed the expression profile of genes related to carbohydrate active enzymes (CAZymes), hydrolases (chitinase, glucanase, protease, and phosphatidase), transporter, and the formation of conidiophore, which responded strongly under carbon starvation.
In order to test whether a considerable variability exists in NKLR expression, we have analyzed the expression profile of CD16, NKp30, NKp46 and NKG2D in 20 healthy donors.
We analyzed the expression profiles of CNTs based on hierarchical clustering to identify representative panels of transcripts expressed in only one specific developmental stage (Fig. 3b) and in all developmental stages analyzed (Fig. 3c).
To elucidate the regulatory roles of rice WRKY factors in defense response to the sheath blight fungus, we have analyzed the expression profiles of rice WRKY family under R. solani infection and methyl jasmonate (MeJA) treatment.
We analyzed the expression profiles of the two very important neuron-specific proteins Neuromodulin (Gap43) and Post-synaptic density protein 95 (PSDlg4 Dlg4) in more detail.
