Cell-based experiments should be carried out in 2.5 5% FBS.
Zentall et al. (2001) (see also Morris and Frey 1997) have suggested that in order to study episodic memory, the test should be unexpected because the episodic information should be encoded automatically; that is, episodic memory experiments should be based on trial-unique learning.
Viability values lower than 50% after the 5 h incubation period are associated with dramatic changes in the estimation of Vu,brain, especially for weak bases and results from the experiments should be discarded.
Based on our results, we suggest that SILAC experiments should be designed to incorporate label-swap replications for enhanced reliability in expression ratios.
Based on these considerations, we consider the opening time of a GV too large for scattering experiments, and the use of this valve as a source for Stark deceleration experiments should be carefully considered.
Further experiments should be done with controlled dissolved oxygen.
These experiments should be replicated with a bigger sample size.
That would include debate before experiments are undertaken on whether and where experiments should be carried out.
However, more experiments should be performed.
If the results of Experiment 1 are based on genuinely semantic relationships then the spreading activation giving rise to priming in that experiment should be occurring in semantic networks that are not confined to particular stimulus formats or modalities.
Based on this assumption, the sum of the fluorescence across all genes for each microarray experiment should be the same.
