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{{chembox
{{chembox
| Watchedfields = changed
| verifiedrevid = 400096678
| verifiedrevid = 442948129
| Name = '''Fura-2'''
| ImageFile = Fura-2.svg
| Name = Fura-2
| ImageFile = Fura-2.svg
| ImageSize = 200px
| ImageName = Fura-2
| ImageSize = 200px
| ImageName = Fura-2
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
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| ChemSpiderID = 51442
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
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| MolarMass = 636.50 g/mol
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'''Fura-2''', a [[polyamino carboxylic acid]], is a ratiometric [[fluorescent]] dye which binds to free intracellular [[calcium]].<ref>{{cite journal | author=Grynkiewicz, G., Poenie, M., and Tsien, R.Y. | title=A new generation of Ca2+ indicators with greatly improved fluorescence properties* | journal=J. Biol. Chem. | volume=260 | pages=3440–3450 | year=1985 | url=http://tsienlab.ucsd.edu/Publications/Grynkiewicz%201985%20JBC%20-%20New%20Generation%20Ca2+%20Indicators.pdf | pmid=3838314 | issue=6}}</ref> It was the first widely-used dye for [[calcium imaging]], and remains very popular. Fura-2 is excited at 340&nbsp;[[nanometer|nm]] and 380&nbsp;nm of light, and the ratio of the emissions at those wavelengths is directly correlated to the amount of intracellular calcium. Regardless of the presence of calcium, Fura-2 emits at 510&nbsp;nm of light. The use of the ratio automatically cancels out confounding variables, such as variable dye concentration and cell thickness, making Fura-2 one of the most appreciated tools to quantify calcium levels. More recently, genetically-encoded calcium indicators based on spectral variants of the [[green fluorescent protein]], such as [[Cameleon (protein)|Cameleon]]s,<ref>{{cite journal |author=Miyawaki A, Llopis J, Heim R, ''et al.'' |title=Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin |journal=Nature |volume=388 |issue=6645 |pages=882–7 |year=1997 |pmid=9278050 |doi=10.1038/42264}}</ref> have supplemented the use of Fura-2 and other small molecule dyes for calcium imaging.
'''Fura-2''', an [[aminopolycarboxylic acid]], is a ratiometric [[fluorescent]] dye which binds to free intracellular [[calcium]].<ref>{{cite journal |author1=Grynkiewicz, G. |author2=Poenie, M. |author3= Tsien, R.Y. |name-list-style=amp| title=A new generation of Ca2+ indicators with greatly improved fluorescence properties* | journal=J. Biol. Chem. | volume=260 | pages=3440–3450 | date=1985 | url=http://tsienlab.ucsd.edu/Publications/Grynkiewicz%201985%20JBC%20-%20New%20Generation%20Ca2+%20Indicators.pdf | pmid=3838314 | issue=6|doi=10.1016/S0021-9258(19)83641-4 |doi-access=free }}</ref> It was the first widely used dye for [[calcium imaging]], and remains very popular. Fura-2 is excited at 340&nbsp;[[nanometer|nm]] and 380&nbsp;nm of light, and the ratio of the emissions at those wavelengths is directly related to the amount of intracellular calcium. Regardless of the presence of calcium, Fura-2 emits at 510&nbsp;nm of light. The use of the ratio automatically cancels out confounding variables, such as variable dye concentration and cell thickness, making Fura-2 one of the most appreciated tools to quantify calcium levels. The high photon yield of fura-2 allowed the first real time (video rate) measurements of calcium inside living cells in 1986.<ref>{{cite journal |last1=Cannell |first1=MB |last2=Berlin |first2=JR |last3=Lederer |first3=WJ |title=Intracellular calcium in cardiac myocytes: calcium transients measured using fluorescence imaging |journal=Society of General Physiologists Series |volume=42 |pages=201–14 |year=1987 |pmid=3505361 }}</ref> More recently, genetically encoded calcium indicators based on spectral variants of the [[green fluorescent protein]], such as [[Cameleon (protein)|Cameleon]]s,<ref>{{cite journal |last1=Tsien |first1=Roger Y. |last2=Miyawaki |first2=Atsushi |last3=Llopis |first3=Juan |last4=Heim |first4=Roger |last5=McCaffery |first5=J. Michael |last6=Adams |first6=Joseph A. |last7=Ikura |first7=Mitsuhiko |title=Fluorescent indicators for Ca<sup>2+</sup>based on green fluorescent proteins and calmodulin |journal=Nature |volume=388 |issue=6645 |pages=882–7 |date=1997 |pmid=9278050 |doi=10.1038/42264|bibcode=1997Natur.388..882M |s2cid=13745050 |doi-access=free }}</ref> have supplemented the use of Fura-2 and other small molecule dyes for calcium imaging, but Fura-2 remains faster.


==See also==
==See also==
* [[Fura-2AM]], a membrane-permeable derivative of Fura-2
* [[Fura-2AM]], a membrane-permeant derivative of Fura-2
*[[Indo-1]]
*[[Indo-1]]

==External links==
* [http://www.fura-2.com Fura-2 Information site]


==References==
==References==
{{reflist}}
<references/>


[[Category:Biochemistry methods]]
[[Category:Biochemistry methods]]
[[Category:Cell culture reagents]]
[[Category:Cell imaging]]
[[Category:Cell imaging]]
[[Category:Chelating agents]]
[[Category:Chelating agents]]
[[Category:Fluorescent dyes]]
[[Category:Fluorescent dyes]]
[[Category:Oxazoles]]
[[Category:Oxazoles]]
[[Category:Benzofurans]]
[[Category:Benzofuran ethers at the benzene ring]]
[[Category:Potassium compounds]]
[[Category:Potassium compounds]]
[[Category:Phenol ethers]]
[[Category:Hydroquinone ethers]]
[[Category:Glycol ethers]]

[[de:Fura-2]]
[[Category:Anilines]]