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Titlebook: Calcium Signaling Protocols; David G. Lambert,Richard D. Rainbow Book 2013Latest edition Springer Science+Business Media, LLC 2013 Calcium

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發(fā)表于 2025-3-21 18:06:05 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Calcium Signaling Protocols
編輯David G. Lambert,Richard D. Rainbow
視頻videohttp://file.papertrans.cn/221/220785/220785.mp4
概述Combines brand new protocols with heavily revised and improved methodologies.Features lab-ready procedures with step-by-step instruction.Includes expert tips and key implementation advice to ensure su
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Calcium Signaling Protocols;  David G. Lambert,Richard D. Rainbow Book 2013Latest edition Springer Science+Business Media, LLC 2013 Calcium
描述.The regulation of intracellular Ca.2+. has continued to be a powerful area of study since the publication of the first and second editions of .Calcium Signaling Protocols., and the developments in the field have also, naturally, continued.? With the third edition, expert contributors explore some of the exciting new molecular techniques that have both enabled new studies of intracellular Ca.2+. regulation and provided much new information on processes.? Comprised of five main section, the book covers theoretical and very simple suspension-based fluorimetric assays, specialist measurement systems, measurement of channel activity, measurement of store release, as well as specialist measurement techniques which include targeted probes, using G-protein chimeras to force Ca.2+. signalling for screening, and genetically encoded sensors.? Written in the highly successful .Methods in Molecular Biology?. series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls..?.Updated and accessible, .Calcium Signaling Protocols,
出版日期Book 2013Latest edition
關(guān)鍵詞Calcium signaling; Channel activity measurement; Intracellular Ca2+; Regulation; Specialist measurement
版次3
doihttps://doi.org/10.1007/978-1-62703-086-1
isbn_softcover978-1-4939-5928-0
isbn_ebook978-1-62703-086-1Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media, LLC 2013
The information of publication is updating

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Measurement of [Ca2+]i in Whole Cell Suspensions Using Fura-2bed in this volume. Whole cell suspensions are loaded with Fura-2 and then placed into a cuvette-based fluorimetric system (measuring 510 nm emission at alternating 340/340 nm excitation). Cells can be stimulated with agonists and antagonists to enable temporal response profiling and concentration–r
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Confocal Microscopy: Theory and Applications for Cellular Signalingful approach to examine cellular structure and function. Allied with the development of suitable tools, it is now possible to interrogate a wide range of structural and functional aspects on both fixed and live cells. Here we describe the basic principles underlying confocal microscopy and provide m
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Ratiometric Ca2+ Measurements Using the FlexStation?Scanning Fluorometer dual-wavelength fluorescent probes. The FlexStation uses a Xenon flashlamp and monochromators for both excitation and emission light to allow the use of a wide range of fluorescent indicators. The system incorporates a fluid transfer system for addition of test compounds from a source plate to the
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Measuring Ca2+ Changes in Multiwell Format Using the Fluorometric Imaging Plate Reader (FLIPR?)onal plate readers is the ability to measure fluorescence emission from multiple wells (96 wells or 384 wells) simultaneously and with high temporal resolution. Consequently, FLIPR has been used extensively to record dynamic intracellular processes such as changes in intracellular Ca. ion concentrat
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Ratiometric [Ca2+]i Measurements in Adherent Cell-Lines Using the NOVOstar Microplate Readere of cellular events. Consequentially, experimental measurement of [Ca.]. is a potent technique for the medical science laboratory. The NOVOstar microplate reader is a versatile system, which may be easily configured to measure [Ca.].. Moreover, the relatively low cost of this system makes it an att
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Whole-Cell Patch-Clamp Recording of Voltage-Sensitive Ca2+ Channel Currents in Single Cells: Heterolle cells, heart pacemaker tissue and endocrine cells. Whole-cell recording is a functional electrophysiological assay that allows real-time measurement of macroscopic VSCC activity at the level of single cells. Using this technique, it is possible to probe the molecular physiology, pharmacology, and
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