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Titlebook: Cell Imaging Techniques; Douglas J. Taatjes,Brooke T. Mossman Book 2006 Humana Press 2006 Microarray.cell biology.electron microscopy.gene

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樓主: Clinton
21#
發(fā)表于 2025-3-25 07:11:25 | 只看該作者
22#
發(fā)表于 2025-3-25 10:37:41 | 只看該作者
23#
發(fā)表于 2025-3-25 13:13:21 | 只看該作者
Visualizing Calcium Signaling in Cells by Digitized Wide-Field and Confocal Fluorescent Microscopy,al [Ca.] gradients. This chapter describes the application of wide-field digitized video fluorescence microfluorometry and confocal microscopy to quantitatively image Ca. in cells with high temporal and spatial resolution.
24#
發(fā)表于 2025-3-25 18:16:00 | 只看該作者
25#
發(fā)表于 2025-3-25 20:46:54 | 只看該作者
26#
發(fā)表于 2025-3-26 00:14:48 | 只看該作者
27#
發(fā)表于 2025-3-26 05:20:59 | 只看該作者
https://doi.org/10.1007/978-981-99-7070-4rescence, it can be separated easily from multiple fluorescent probes. It is already proving useful in imaging collagen with high sensitivity in various tissues, including cirrhotic liver, normal and carious teeth, and surgical repair of tendons.
28#
發(fā)表于 2025-3-26 11:40:02 | 只看該作者
https://doi.org/10.1007/978-981-99-7923-3 data that are accurate with the necessary resolution, sensitivity, and precision. Utilization of this proposed testing approach will help eliminate the subjective nature of assessing the CLSM and allow different machines to be compared. These tests are essential if one is to make intensity measurem
29#
發(fā)表于 2025-3-26 13:45:30 | 只看該作者
30#
發(fā)表于 2025-3-26 20:32:41 | 只看該作者
https://doi.org/10.1007/978-981-99-8561-6nsmission and fluorescence microscopy. The height of the scanning probe is controlled by atomic force interactions between the specimen surface and the probe tip. The control signal can be used for the production of a topographic (nonoptical) image that can be acquired simultaneously. In this chapte
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