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The CRAC Channel

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Cover of 'The CRAC Channel'

Table of Contents

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    Book Overview
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    Chapter 1 Patch-Clamp Recording of the CRAC Channel Current in STIM-Orai Overexpressing Cells
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    Chapter 2 Fluorescence-Based Ratiometric Measurement of CRAC Channel Activity in STIM-Orai-Overexpressing HEK-293 Cells
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    Chapter 3 Recording SOCE Activity in Neurons by Patch-Clamp Electrophysiology and Microfluorometric Calcium Imaging
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    Chapter 4 Mn2+ Quenching Assay for Store-Operated Calcium Entry
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    Chapter 5 Fluorescence-Based Measurements of Store-Operated Ca2+ Entry in Cancer Cells Using Fluo-4 and Confocal Live-Cell Imaging
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    Chapter 6 Fluorescence-Based Measurements of the CRAC Channel Activity in Cell Populations
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    Chapter 7 Indirect Measurement of CRAC Channel Activity Using NFAT Nuclear Translocation by Flow Cytometry in Jurkat Cells
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    Chapter 8 CRAC Channel Components Quantitative Expression (In Tissues and Cell Lines) Using qPCR
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    Chapter 9 Western Blotting and Co-immunoprecipitation of Endogenous STIM/ORAI and Protein Partners
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    Chapter 10 Study of Endogenous CRAC Channels in Human Mast Cells Using an Adenoviral Delivery System to Transduce Cells with Orai-Targeting shRNAs or with cDNAs Expressing Dominant-Negative Orai Channel Mutations
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    Chapter 11 Store-Operated Ca2+ Entry in Drosophila Primary Neuronal Cultures
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    Chapter 12 Study of the Endogenous CRAC Channel Using shRNA-Mediated Gene Silencing
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    Chapter 13 Engineered Cross-Linking to Study the Pore Architecture of the CRAC Channel
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    Chapter 14 Measurement of the CRAC Channel Fast Ca2+-Dependent Inactivation (FCDI)
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    Chapter 15 High-Resolution Imaging of STIM/Orai Subcellular Localization Using Array Confocal Laser Scanning Microscopy
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    Chapter 16 Single-Channel Single-Molecule Detection (SC-SMD) System
Attention for Chapter 6: Fluorescence-Based Measurements of the CRAC Channel Activity in Cell Populations
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Chapter title
Fluorescence-Based Measurements of the CRAC Channel Activity in Cell Populations
Chapter number 6
Book title
The CRAC Channel
Published in
Methods in molecular biology, September 2018
DOI 10.1007/978-1-4939-8704-7_6
Pubmed ID
Book ISBNs
978-1-4939-8702-3, 978-1-4939-8704-7
Authors

Pedro C. Redondo, Alejandro Berna-Erro, Natalia Dionisio, Juan A. Rosado, Redondo, Pedro C., Berna-Erro, Alejandro, Dionisio, Natalia, Rosado, Juan A.

Abstract

Cytosolic Ca2+ plays an important role in cellular biology, and since its identification as a second messenger, a number of techniques and methods to analyze the changes in cytosolic Ca2+ concentration ([Ca2+]c) induced by physiological agonists have been developed. Changes in [Ca2+]c might be determined in single cells or in cell populations. Measurement in single cells allows to determine changes in [Ca2+]c at a subcellular level but often results in heterogeneous responses among cells. Determination of intracellular Ca2+ mobilization at the cell population level reduces this heterogeneity and allows [Ca2+]c measurements in small cells that load little amounts of indicator. Here, we describe the measurement of agonist-evoked changes in [Ca2+]c associated with Ca2+ influx in cell populations.

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Mendeley readers

The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 1 50%
Student > Bachelor 1 50%
Readers by discipline Count As %
Unspecified 1 50%
Biochemistry, Genetics and Molecular Biology 1 50%