Body temperature was recorded every 15 minutes throughout both experiments using a device (DST micro-T, Star-Oddi, Reykjavik, Iceland) implanted in the peritoneal cavity 14 days before challenge.
Both experiments used a two-stage transfer design.
Both experiments used a completely randomised block design, with two replicates in experiment 1 and three replicates in experiment 2. Four heifers (24 ± 2 months and 306 ± 56.7 kg) were used in experiment 1.
Both experiments used a factorial design combining three larval stocking densities (D-stage: 2, 6 & 10 larvae mL−1; umbo-stage: 1, 3 & 5 larvae mL−1) and three rations (D-stage: 5, 10 & 15 cells mL−1; umbo-stage: 10, 15 & 20 cells mL−1).
Both experiments used a similar protocol of isometric force production but the present results failed to reveal any changes in the control strategy adopted by the subjects.
Both experiments used a 2 × 2 design with Item (Old vs. New) and Prime (Related vs. Unrelated) as within-subjects factors.
Both experiments used a repeated-measures design, investigating the effects of Repetition (same-face identity/same-scene, different-face identity/different-scene), and Image Size (same-size, vary-size).
To understand the possible formation mechanisms of brominated organic species in iron ore sintering, both full-scale and laboratory experiments using an experimental sintering process were carried out.
The potential role of either or both is supported by the heterologous experiments using an RNA reporter system, in which expression of either constitutively active Rac2 or Rac1 was sufficient to stabilize the otherwise destabilized, uPAR class II ARE-bearing β-globin transcript.
Thus, we started to look for a more versatile tag system that would allow us to carry out both bioimaging and biochemical experiments using a single tag.
