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The results of Newton's assay were used, among other things, to set the bewildering, constantly shifting exchange rates that were a part of daily commercial life in England and America in the early eighteenth century.
Five micrograms of purified proteins, as measured using the Bradford assay, were used in each experiment.
The sets of three wells for the MTT assay were used for each experimental variable.
DNA blot and PCR assay were used to determine the homogeneity of knockout mutants.
Ames test and Comet assay were used to follow the genotoxicity during the degradation of the studied compounds.
Histology analysis and a blood assay were used to evaluate the in vivo biocompatibility of MoS2 ICG.
The results of the pull-down assay were used to evaluate if these models were reasonable (See Extended Experimental Procedures).
A quartz crystal microbalance and immunological sandwich assay were used to demonstrate that the HGFI-coated MWCNTs can be used to immobilize human immunoglobulin G in solution.
Fourier Transform Infrared (FTIR) spectroscopy and the azure A assay were used to evaluate interactions between dendrimers and enoxaparin.
Western blotting and ERK blocking assay were used to examine the role of ERK1/2 signaling pathway on PS activity.
Northern blot analysis and enzyme-linked immunosorbent assay were used to evaluate messenger RNA and protein levels, respectively.
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