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From the time of Millikan's original experiment, this method offered convincing proof that electric charge exists in basic natural units.
For our preliminary experiment, this method was innovatively combined with interference lithography (hologram lithography).
Within a single experiment, this method can sequence the exonic regions of hundreds of genes in tens of samples for sequence and structural variation using as little as 1 μg of input DNA per sample.
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With a very limited number of experiments, this method allowed to obtain first encouraging results.
As we demonstrate in our experiments, this method can be used to enable large-scale evaluations and complement the user studies that are typically used for this purpose.
For the FITC/InlA-bead experiments this method could not be used because the pH within the phagosome equilibrated with the cytoplasm after cells were fixed.
With reconstruction experiments this method showed a detection limit range of 10-50 cells/PCR.
For the thermodynamics experiments, this method was repeated at the following temperatures: 5, 10, 15, 20, 25, and 30°C.
In control experiments, this method was compared with an alternative procedure, in which the dye is introduced into the t-tubules before skinning [18].
In some experiments this method was used to load fluo-3 into the re-sealed t-tubules (20 μM, 10 min exposure).
It can be seen from the experiment that this method can obtain accurate, smooth, and robust results.
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CEO of Professional Science Editing for Scientists @ prosciediting.com