Chemical Name: N,N'-[[3',6'-Bis(acetyloxy)-oxospiro[isobenzofuran-1-(3H),9'-(9H)xanthene]-4',5'-diyl]bis(methylene)]bis[N-[2-(acetyloxy)methoxy]-2-oxoethyl]glycine 1,1'-bis[(acetyloxy)methyl] ester
Biological ActivityCell permeable, non-fluorescent compound for monitoring cell viability, chemotaxis, cell adhesion and multidrug resistance; hydrolyzed by intracellular esterases to become fluorescent calcein in living cells..
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Tocris products are intended for laboratory research use only, unless stated otherwise.
Prostaglandin E2 activates and utilizes mTORC2 as a central signaling locus for the regulation of mast cell chemotaxis and mediator release.
Kuehn et al.
The use of calcein acetomethylester (AM)-labelled polymorphonuclear cells in a polycarbonate filter chemotaxis assay.
De Gendt et al.
Membrane topology and glycosylation of the human multidrug resistance-associated protein.
Bakos et al.
Direct demonstration of mechanically induced release of cellular UTP and its implication for uridine nucleotide receptor activation.
Lazarowski et al.
Citations for Calcein AM
The citations listed below are publications that use Tocris products. Selected citations for Calcein AM include:
3 Citations: Showing 1 - 3
Interleukin-1β induces CXCR3-mediated chemotaxis to promote umbilical cord mesenchymal stem cell transendothelial migration.
Authors: Guo Et al.
Stem Cell Res Ther 2018;9:281
CD90 determined two subpopulations of glioma-associated mesenchymal stem cells with different roles in tumour progression.
Authors: Zhang Et al.
Cell Death Dis 2018;9:1101
Loss of the mitochondrial kinase PINK1 does not alter platelet function.
Authors: Walsh Et al.
Sci Rep 2018;8:14377
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For analyzing cellular toxicity in neurons