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In kidney, lung, and spleen, the dual label experiment using C-labeled non-hydrolyzable retinyl ether along with H-retinyl palmitate [18] showed that these tissues took up equal amounts of C- and H-label indicating that REH activity of LPL is not essential for retinoid uptake in these tissues.
Additionally, we used the correct classification rate (CCR) to evaluate accuracy for the classification of the CS label experiment.
In cardiac muscle the dual label experiment with H-retinyl palmitate and non-cleavable C-retinyl ether resulted in a H C ratio of 1 52 [1 52
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Double label experiments provided evidence that α4 and β2 subunits co-localize on small RGCs.
We performed single label experiments to exclude over-bleeding between the channels.
There was an average of 4.7 MCTP1-positive cells per taste bud section in single label experiments.
To confirm the results, in separate single label experiments Paxillin was stained using the Alexa598 red conjugate (data not shown).
Figure 1 Sound labeling experiment interface.
The radiolabelling yield and radiochemical purity were determined after each labelling experiment.
The mechanistic pathway of the multicomponent reaction was briefly investigated using an 18O labelling experiment.
In a typical isotopic labeling experiment, the goal is to compare protein abundances between two samples.
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