Topic Introduction

Ca2+-Sensitive Fluorescent Dyes and Intracellular Ca2+ Imaging

  1. Michael Sanderson3
  1. 1Babraham Institute, Babraham, Cambridge, CB22 3AT, United Kingdom;
  2. 2Department of Life, Health and Chemical Sciences, The Open University, Walton Hall, Milton Keynes, MK7 6AA, United Kingdom;
  3. 3Department of Microbiology and Physiology Systems, University of Massachusetts Medical School, Worcester, Massachusetts 01655;
  4. 4McMaster Stem Cell and Cancer Research Institute, Faculty of Health Sciences, McMaster University, MDCL 5029, Hamilton, Ontario L8S4L8, Canada

    Abstract

    Imaging Ca2+-sensitive fluorescent indicators provides a common approach for studying Ca2+ signals in many contexts. Fluorescent indicators are particularly useful for measuring acute Ca2+ changes in a relatively noninvasive manner. The availability of indicators that can be targeted to specific cellular domains, coupled with variations in affinity, brightness or spectral characteristics, provides tools for exploring spatially and temporally diverse Ca2+ signals, and moreover, multiplexing the readout of Ca2+ with other cellular functions. This article aims to give the novice experimentalist some insight into the considerations and potential pitfalls that impinge on the use of fluorescent Ca2+ indicators.

    Footnotes

    • 5 Correspondence: martin.bootman{at}babraham.ac.uk

    | Table of Contents