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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 4: Mn2+ Quenching Assay for Store-Operated Calcium Entry
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Chapter title
Mn2+ Quenching Assay for Store-Operated Calcium Entry
Chapter number 4
Book title
The CRAC Channel
Published in
Methods in molecular biology, September 2018
DOI 10.1007/978-1-4939-8704-7_4
Pubmed ID
Book ISBNs
978-1-4939-8702-3, 978-1-4939-8704-7
Authors

Zui Pan, Sangyong Choi, Yanhong Luo, Pan, Zui, Choi, Sangyong, Luo, Yanhong

Abstract

Store-operated Ca2+ entry (SOCE) pathway plays important roles in many cellular processes, which is largely studied by using fluorescent Ca2+ indicator, Fura-2. Extracellular Mn2+ is able to cross the plasma membrane through SOCE and quenches the fluorescence signals from Fura-2. Thus, the fluorescence quenching rate by Mn2+ composes a convenient assay to monitor the extent of SOCE. This chapter describes an experimental method of Mn2+ quenching assay for both cultured esophageal epithelial and skeletal muscle cells. It also explains how to perform a quantitative analysis of graded SOCE.

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Mendeley readers

The data shown below were compiled from readership statistics for 19 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 19 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 21%
Student > Doctoral Student 3 16%
Student > Postgraduate 3 16%
Professor 1 5%
Other 1 5%
Other 2 11%
Unknown 5 26%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 21%
Neuroscience 3 16%
Agricultural and Biological Sciences 3 16%
Unspecified 1 5%
Medicine and Dentistry 1 5%
Other 1 5%
Unknown 6 32%