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Additionally, a drastic increase in solution viscosity due to the formation of giant molecules was monitored during polymerization.

The change in the length of individual ssDNA molecules was monitored by the position change of the bead linked to the ssDNA.

The controlled release of free SN-38 molecules was monitored by high-performance liquid chromatography (HPLC).

Internalization of the "old" Ab-engaged receptor was therefore monitored in red, whereas reexpression on the membrane of "new" receptor molecules was monitored in green.

The activity of transglutaminase, a calcium-dependent enzyme that accelerates the cross-linkage of polypeptide chains by catalyzing the covalent binding of polyamines to g-glutamine residues of protein molecules, was monitored in the serum and CSF of SALS patients.

The effect of PDT on the function of adhesion molecules was monitored by determining the ability of neutrophils to adhere to EMT6 microvessels in frozen-tissue sections under mechanical shear following in vivo PDT treatment.

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The geometric motion of TEA molecules were monitored in real time across this patterned c(4 × 2) surface.

The interaction between membrane-bound hydrophobic compounds and free hydrophilic molecules is monitored in real-time and with high sensitivity and selectivity by combined SPS/SPFS.

Upon mitogenic activation, secreted IFN-γ and TNF-α molecules were monitored by performing square wave voltammetry (SWV) at different time points at individually addressable electrodes.

The system is designed such that a sample is taken from the fermentor, the metabolism of microbial cells is instantaneously arrested, the cells are lysed in order to release intracellular compounds and in a subsequent binding assay the content of target molecules is monitored.

The flux of molecules is monitored to retain folding intermediates and target misfolded molecules to ER-associated degradation (ERAD) pathways.

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