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文献和实验Measuring Microchannel Electroosmotic Mobility and Zeta Potential by the Current Monitoring Method
that leads to bulk solution movement. The goal of this laboratory is to experimentally determine the fixed channel surface charge (zeta potential) and electroosmotic mobility associated with a given microchannel substrate material and buffer solution, using
Control of Mitotic Entry After DNA Damage in Drosophila
the collection of embryos and larvae, irradiation with x-rays to damage DNA, and fixing and staining of tissues with an antibody to phosphorylated histone H3 to measure the mitotic index. These methods should be useful in identifying potential mutants
MitoProbe DiIC1 Mitochondrial Membrane Potential Protocol
, phosphate-buffered saline, or other buffer at approximately 1 x 106 cells/mL. 2) For the control tube, add 1 μL of 50 mM CCCP (supplied with the kit, 50 μM final concentration) and incubate the cells at 37°C for 5 minutes.Note: CCCP
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