Our experiments presented here are a combination based on those two approaches mentioned above.
In our experiments presented here we used cantilever-arrays with soft spring constants (0.02 N/m) but measured at higher modes (mode 13, 14 or 15) of vibration to increase the sensitivity [5], [27], [28].
In our experiments presented in the section below, flank_region_size was set to the default value of 4,000.
Our experiments presented in the current study provided evidence for non-linear dependence of ER-related tresponsetional response on the level of ERα expression.
For our experiments presented in this study, the lambda subtype of AL-LC and kappa subtype of Con-LC proteins were used.
However, the results of our experiments presented an intriguing and opposite picture in that a large number of Bhsp65-inducible genes were rather upregulated in Bhsp65-tolerized rats compared to the control preclinical arthritis rats.
Our experiments presented in this manuscript showed that classical, autoclaved PPD was essentially a mixture of peptide fragments which could not be sufficiently resolved by SDS-PAGE, 2-DE or Western blot analysis to characterize the antibody responses of our experimental cattle.
This paper describes the design of our experiment, presents our results, and discusses directions for future research.
Our experiment presents test validation, calibration and measurement error correction methodology that can be successfully applied to ensure and improve accuracy of IHC Ki67 LI estimation by DIA.
Although useful for proof of principle studies like presented here, unmodified LPEI is not the ideal carrier for targeting transgene expression to the tumor after systemic injection: In our experiment presented here, the level of luciferase activity in tumors strongly varied between individual animals (CMV driven plasmid: 4 high, 2 low, AFP driven plasmid: 3 high, 3 low).
