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The most common sensing format is the homogeneous assay (Figure 2).
This could be proven in the ER Calux assay (Figure 4).
Purified Can was used as a control for CA activity assay (Figure 5A).
Four independent transgenic lines confirmed by Southern blot assay (Figure 1B) were selected for further investigation.
Catalase overexpression was confirmed by the zymograph assay (Figure 1B).
The down-regulation of RPA1 was evaluated by both real-time quantitative RT-PCR assay (Figure 5A) and Western blotting assay (Figure 5B).
No islets from wildtype mice were overtly angiogenic in this assay (Figure 1c).
Mitochondrial structure and quantity appeared normal by this assay (figure 2B).
The kinetics of fibril formation was primarily followed using a ThT-binding assay (Figure 3).
Maximal male attraction was found using an amount of 25 WE per assay (Figure 2B).
Stable HIF-1α expression was confirmed by HRE (hypoxia responsive element) luciferase reporter assay (Figure 1C).
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