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Titlebook: cAMP Signaling; Methods and Protocol Manuela Zaccolo Book 2015 Springer Science+Business Media New York 2015 Adenosine 3′,5′-monophosphate.

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發(fā)表于 2025-3-21 19:48:17 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱cAMP Signaling
副標(biāo)題Methods and Protocol
編輯Manuela Zaccolo
視頻videohttp://file.papertrans.cn/243/242718/242718.mp4
概述Includes cutting-edge methods and protocols on cAMP signaling.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from experts
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: cAMP Signaling; Methods and Protocol Manuela Zaccolo Book 2015 Springer Science+Business Media New York 2015 Adenosine 3′,5′-monophosphate.
描述.This detailed volume encompasses new technological developments that specifically address questions related to adenosine 3′,5′-monophosphate (cAMP) compartmentalization, that probe relevant protein-protein interactions, that increase the spatial and temporal resolution of cAMP signal detection, and that can facilitate integration of the mounting complexity of the information that is becoming available on this signaling system. cAMP, the prototypical intracellular second messenger, regulates a large variety of cellular functions and biological processes, including gene transcription, cell metabolism, proliferation, development, as well as more specialized functions depending on the cell type, so the realization of its extremely complex spatial organization and local regulation is providing novel mechanistic insight into cell physiology and is producing a novel framework for the identification of disease mechanisms. Written in the highly successful .Methods in Molecular Biology. series format, chapters include introduction to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting an
出版日期Book 2015
關(guān)鍵詞Adenosine 3′,5′-monophosphate; Cellular function; Disease mechanisms; Protein kinase A (PKA); Signaling
版次1
doihttps://doi.org/10.1007/978-1-4939-2537-7
isbn_softcover978-1-4939-4950-2
isbn_ebook978-1-4939-2537-7Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 2015
The information of publication is updating

書目名稱cAMP Signaling影響因子(影響力)




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Recording Intracellular cAMP Levels with EPAC-Based FRET Sensors by Fluorescence Lifetime Imaging,wnstream cellular effectors. FRET-based sensors are ideal to visualize and measure these rapid changes of second messenger concentrations in time and place. Here, we describe the use of EPAC-based FRET sensors to measure cAMP with spatiotemporal resolution in cells by fluorescence lifetime imaging (
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A Novel Approach Combining Real-Time Imaging and the Patch-Clamp Technique to Calibrate FRET-Based cAMP) signaling and compartmentalization in living cells. These sensors allow estimation of relative changes of cAMP levels in real-time and intact cells. However, one of their major shortcomings is that they do not easily allow direct measurement of cAMP concentrations. This is mainly due to the fa
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Channel-Based Reporters for cAMP Detection,hat have been modified to transduce cAMP concentrations into electrical or fluorescent readouts that can be readily detected using patch clamp amplifiers, photomultiplier tubes, or cameras. Here we describe two complementary approaches for the detection and measurement of cAMP signals near the plasm
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Imaging Sub-plasma Membrane cAMP Dynamics with Fluorescent Translocation Reporters,rs, a large number of tools for cAMP measurements have been developed. While most cAMP reporters are designed to undergo changes in fluorescence resonance energy transfer (FRET), there are alternative techniques with advantages for certain applications. Here, we describe protocols for cAMP measureme
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