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The support effect on the activity of hydrotreating catalysts using model molecules was analyzed for catalysts supported on TiO2, SiO2 and MgO.
These DNA constructs were co-expressed in HEK-293 cells and the assembly of heterogeneous triple-helical mini-procollagen VII molecules was analyzed.
Each soluble fraction of MH7A cells harboring plasmid-encoded affibody molecules was analyzed via western blot for the expression of p-ERK and actin at 16 and 24 h after TNF-α stimulation.
(B) Western blot analysis of each soluble fraction from MH7A cells harboring plasmid-encoded affibody protein molecules was analyzed at 48 and 72 h after the introduction of the plasmid into MH7A cells.
The expression of various cell surface molecules was analyzed by flow cytometry as described in materials and methods.
Colocalization between two different molecules was analyzed in segmented images with the Imaris software (release 4.2; Bitplane, Zurich, Switzerland; for details, see ref. [34]).
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Cytokines, chemokines, and adhesion molecules were analyzed on Evidence® array biochip analyzer (Randox Laboratories Ltd., Crumlin, UK).
The expressions of surface and cytoplasmic class II molecules were analyzed by flow cytometry.
p53 was immunoprecipitated and eluted with 0.1 M glycine (pH 2.5) and the associated molecules were analyzed by IB.
The eluted molecules were analyzed by an Orbitrap Velos mass spectrometer (ThermoFisher Scientific, San Jose, CA) with a targeted MS/MS method.
The intended result was a sort of mental chemistry, in which sensory experiences, analogous to molecules, were analyzed into their constituent elements, analogous to atoms.
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elements was analyzed
pathways was analyzed
compounds was analyzed
particles was analyzed
species was analyzed
clips was analyzed
models was analyzed
molecules was prepared
molecules was carried
molecules was measured
molecules was confirmed
molecules was developed
molecules was performed
molecules was kept
molecules was studied
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