The error bars indicate the SE for three replicate experiments.
Each vertical bar represents Mean ± SE for four measurements from individual plants.
Physiological data and qPCR results are reported as the mean ± the standard error (SE) for six mice.
Lower panels: quantification of results of Western blots, as means ± SE for eight mice of each genotype.
We counted the number of PAS-positive cells per section using a light microscope, and results are presented as mean ± SE for four sections per mouse lung.
The data plotted are mean ± SE for nine repeats, which were simultaneously fit to derive the KD and error estimate shown.
Our analysis was not expected to illuminate the process of heterocyst differentiation, per se, for three interrelated reasons: (i) Steady state cultures were needed for prospective metabolic flux analysis.
Since users and sensors are grouped into three groups, respectively, the SE is defined as the average SEs for three groups.
Quantitative values are mean ± SE of four amplifications for placenta and three for maternal liver for each transporter gene.
A similar analysis was conducted for Ca, Mg, Fe, Cu, Mn, B, V, Si, Zn and Se for all eight species.
This leads to the following definitions: SE = TP / (TP + FN + F P s ) SP = TN / (TN + F P n ) PR = TP / (TP + F P n + F P s ) FM = 2 · PR · SE / (PR + SE ) For all three benchmark examples, we evaluated the inference by those statistical measures showing the reproduction of the system structure and time series by the model.
