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We further confirmed the specificity of this drug delivery carrier to the desired location by using confocal imaging, while NO release by HAase was confirmed via diaminofluorescein-2 diacetate assay.
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Using confocal imaging to enhance visibility in weakly scattering environments.
Using confocal imaging, we observed a tonotopic gradient in the concentration of proteinaceous Ca(2+) buffers.
Expression and localization were verified using confocal imaging.
By using confocal microscopy imaging, it has been observed that SWCNTs have the ability to incorporate inside the cells, whereas MWCNTs are not incorporated into the cells.
To further confirm the regulation of nuclear localization of the SWI/SNF proteins by oxygen, we quantitatively examined and compared their distribution in live hypoxic and normoxic cells, by using confocal fluorescent live cell imaging.
Tumor cells were observed by using confocal laser scanning microscopy (CLSM; LSM 410, Zeiss, Jena, Germany) with an imaging software.
We tested this concept by Ca2+ imaging experiments using confocal line scanning fluorescence microscopy.
Data were verified using confocal laser scanning microscopy imaging.
When imaging embryos using confocal microscopy, the microfluidic device previously described [12] was coupled to a multi-point confocal system.
We have exposed the cells to H2O2 and CCCP as described above followed by real-time imaging of ratio change and DsRed at an interval of 15 min using confocal microscope.
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