A 340/380 nm light emitting diode illuminator for Fura-2 AM ratiometric Ca2+ imaging of live cells with better than 5 nM precision

Research output: Contribution to conferencePoster

Abstract

Cytosolic Ca2+ plays an integral role in cells and the study of its dynamics can reveal much about biological processes [1]. Fura-2 can provide quantitative data on cytosolic Ca2+ changes by exciting at 340 nm and 380 nm and taking the ratio of the emission at both wavelengths [2]. Traditionally for this type of imaging an arc lamp had to be used for illumination as LEDs of the appropriate wavelengths were not available [3]. LEDs hold advantages over arc lamps by exhibiting high amplitude stability and the ability to rapidly switch between wavelengths. We aimed to test a new 340/380 nm LED system for use in ratiometric Fura-2 AM Ca2+ imaging and present results using tsA-201 cells and hippocampal neurons.
LanguageEnglish
Number of pages1
Publication statusPublished - 4 Jul 2017
EventMicroscience Microscopy Congress 2017 - Manchester, United Kingdom
Duration: 3 Jul 20176 Jul 2017

Conference

ConferenceMicroscience Microscopy Congress 2017
CountryUnited Kingdom
CityManchester
Period3/07/176/07/17

Fingerprint

Fura-2
Biological Phenomena
Light
Lighting
Neurons

Keywords

  • cell imaging
  • light emitting diode
  • LED wavelength

Cite this

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title = "A 340/380 nm light emitting diode illuminator for Fura-2 AM ratiometric Ca2+ imaging of live cells with better than 5 nM precision",
abstract = "Cytosolic Ca2+ plays an integral role in cells and the study of its dynamics can reveal much about biological processes [1]. Fura-2 can provide quantitative data on cytosolic Ca2+ changes by exciting at 340 nm and 380 nm and taking the ratio of the emission at both wavelengths [2]. Traditionally for this type of imaging an arc lamp had to be used for illumination as LEDs of the appropriate wavelengths were not available [3]. LEDs hold advantages over arc lamps by exhibiting high amplitude stability and the ability to rapidly switch between wavelengths. We aimed to test a new 340/380 nm LED system for use in ratiometric Fura-2 AM Ca2+ imaging and present results using tsA-201 cells and hippocampal neurons.",
keywords = "cell imaging, light emitting diode, LED wavelength",
author = "Tinning, {Peter William} and Aimee Franssen and Hridi, {Shehla Unaiza} and Trevor Bushell and Gail McConnell",
year = "2017",
month = "7",
day = "4",
language = "English",
note = "Microscience Microscopy Congress 2017 ; Conference date: 03-07-2017 Through 06-07-2017",

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A 340/380 nm light emitting diode illuminator for Fura-2 AM ratiometric Ca2+ imaging of live cells with better than 5 nM precision. / Tinning, Peter William; Franssen, Aimee; Hridi, Shehla Unaiza; Bushell, Trevor; McConnell, Gail.

2017. Poster session presented at Microscience Microscopy Congress 2017, Manchester, United Kingdom.

Research output: Contribution to conferencePoster

TY - CONF

T1 - A 340/380 nm light emitting diode illuminator for Fura-2 AM ratiometric Ca2+ imaging of live cells with better than 5 nM precision

AU - Tinning, Peter William

AU - Franssen, Aimee

AU - Hridi, Shehla Unaiza

AU - Bushell, Trevor

AU - McConnell, Gail

PY - 2017/7/4

Y1 - 2017/7/4

N2 - Cytosolic Ca2+ plays an integral role in cells and the study of its dynamics can reveal much about biological processes [1]. Fura-2 can provide quantitative data on cytosolic Ca2+ changes by exciting at 340 nm and 380 nm and taking the ratio of the emission at both wavelengths [2]. Traditionally for this type of imaging an arc lamp had to be used for illumination as LEDs of the appropriate wavelengths were not available [3]. LEDs hold advantages over arc lamps by exhibiting high amplitude stability and the ability to rapidly switch between wavelengths. We aimed to test a new 340/380 nm LED system for use in ratiometric Fura-2 AM Ca2+ imaging and present results using tsA-201 cells and hippocampal neurons.

AB - Cytosolic Ca2+ plays an integral role in cells and the study of its dynamics can reveal much about biological processes [1]. Fura-2 can provide quantitative data on cytosolic Ca2+ changes by exciting at 340 nm and 380 nm and taking the ratio of the emission at both wavelengths [2]. Traditionally for this type of imaging an arc lamp had to be used for illumination as LEDs of the appropriate wavelengths were not available [3]. LEDs hold advantages over arc lamps by exhibiting high amplitude stability and the ability to rapidly switch between wavelengths. We aimed to test a new 340/380 nm LED system for use in ratiometric Fura-2 AM Ca2+ imaging and present results using tsA-201 cells and hippocampal neurons.

KW - cell imaging

KW - light emitting diode

KW - LED wavelength

UR - http://www.mmc-series.org.uk/

M3 - Poster

ER -