細(xì)胞內(nèi)鈣通量測(cè)定法是監(jiān)測(cè)GPCR和鈣通道活性的一種廣泛使用的方法。為了定量細(xì)胞內(nèi)鈣濃度,優(yōu)選比例熒光熒光指示劑
Ex (nm) | - | Em (nm) | - |
分子量 | ~1000 | 溶劑 | Water |
存儲(chǔ)條件 | 在零下15度以下保存, 避免光照 |
細(xì)胞內(nèi)鈣通量測(cè)定法是監(jiān)測(cè)GPCR和鈣通道活性的一種廣泛使用的方法。為了定量細(xì)胞內(nèi)鈣濃度,優(yōu)選比例熒光熒光指示劑,因?yàn)樵摫嚷逝c鈣濃度直接相關(guān)并且與細(xì)胞數(shù)和染料負(fù)載濃度無關(guān)。但是,流行的比例鈣指示劑(例如Fura-2和Indo-1)具有一定的局限性,例如靈敏度較低,紫外線激發(fā),并且與HTS篩選濾光片組不兼容。Cal Red R525 / 650已開發(fā)為新型的488 nm可激發(fā)比例熒光鈣指示劑。Cal Red R525 / 650在488 nm處受到很好的激發(fā),在525 nm和650 nm處有兩次發(fā)射。結(jié)合鈣后 當(dāng)在488 nm激發(fā)時(shí),Cal Red R525 / 650的發(fā)射信號(hào)在525 nm處增加,在650 nm處降低。Cal Red R525 / 650的激發(fā)和發(fā)射波長與普通濾光片組兼容,對(duì)細(xì)胞的損害小,使其成為評(píng)估和篩選GPCR激動(dòng)劑和拮抗劑以及鈣通道靶標(biāo)的強(qiáng)大工具
參考文獻(xiàn)
Ratiometric analysis of fura red by flow cytometry: a technique for monitoring intracellular calcium flux in primary cell subsets
A flow cytometric comparison of Indo-1 to fluo-3 and Fura Red excited with low power lasers for detecting Ca(2+) flux
Use of co-loaded Fluo-3 and Fura Red fluorescent indicators for studying the cytosolic Ca(2+)concentrations distribution in living plant tissue
[Monitoring calcium in outer hair cells with confocal microscopy and fluorescence ratios of fluo-3 and fura-red]
Calcium transient alternans in blood-perfused ischemic hearts: observations with fluorescent indicator fura red
Authors: Wendt ER, Ferry H, Greaves DR, Keshav S.
Journal: PLoS One (2015): e0119532
Authors: Bailey S, Macardle PJ.
Journal: J Immunol Methods (2006): 220
Authors: Walczysko P, Wagner E, Albrechtova JT.
Journal: Cell Calcium (2000): 23
Authors: Su ZL, Li N, Sun YR, Yang J, Wang IM, Jiang SC.
Journal: Shi Yan Sheng Wu Xue Bao (1998): 323
Authors: Wu Y, Clusin WT.
Journal: Am J Physiol (1997): H2161
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