Therefore, proteins spiked in human urine were successfully identified at 500 nM.
Of these candidates, 38 recombinant proteins were successfully identified for their enzyme activity and substrate specificity.
A total of 172 protein groups, 1009 proteins, and 1073 unique peptides were successfully identified.
Seventy spots were successfully identified and finally integrated into 30 proteins.
Although the validation rate was low, a number of drug gene interactions were successfully identified and are now being investigated for protein induction and in vivo effect.
The structural states of lithium and aluminum in those samples were successfully identified by calculation of NMR spectra.
Amplitude dependent, constant stiffness parameters were successfully identified for a multiple-degree-of-freedom (MDOF) nonlinear reduced order model.
Matrix cracking and delamination were successfully identified using the PCT approach and improved location accuracy was achieved.
Sooting limits depending on equivalence ratio and flow velocity (residence time) were successfully identified by the present micro flow reactor.
Twenty-nine and 32 protein spots were successfully identified when cells were treated with 10 and 20 μM QCT, respectively.
Fifteen hits with inhibitory potencies ranging from 2.8 to 118 μM (IC50) against β-secretase were successfully identified.
