Calcein AM

Pricing Availability   Qty
说明: Cell permeable non-fluorescent compound; green-fluorescent in living cells once hydrolyzed. Used for: cell tracing and cell viability monitoring. Application: fluorescent microscopy and flow cytometry
化学名: 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
纯度: ≥90% (HPLC)
说明书
引用文献 (5)
评论 (1)
文献 (1)

生物活性 for Calcein AM

Key information: Calcein AM is a cell permeable non-fluorescent compound, that becomes green fluorescent once hydrolyzed in live cells.

Used for: cell tracing, monitoring cell viability, chemotaxis, cell adhesion and multidrug resistance.

Application: fluorescent microscopy and flow cytometry.

Properties and Photophysical Data: in live cells, non-fluorescent Calcein AM is hydrolyzed by intracellular esterases into green-fluorescent calcein, which is retained in the cytoplasm. Excitation and emission maxima (λ) are 495 nm and 515 nm, respectively.

It is recommended to prepare stock solutions of Calcein AM in DMSO.

Optical Data for Calcein AM

Calcein AM Dye Spectra
Emission Color Green
λabs 495 nm
λem 515 nm
Cell Permeable Yes
Application Flow Cytometry, Fluorescent Microscopy

Plan Your Experiments

Use our spectra viewer to interactively plan your experiments, assessing multiplexing options. View the excitation and emission spectra for our fluorescent dye range and other commonly used dyes.

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技术数据 for Calcein AM

分子量 994.86
公式 C46H46N2O23
储存 Store at -20°C
纯度 ≥90% (HPLC)
CAS Number 890090-35-4
PubChem ID 4126474
InChI Key XKFSBWQWNMZWFA-UHFFFAOYSA-N
Smiles O=C(C)OC3=C(CN(CC(OCOC(C)=O)=O)CC(OCOC(C)=O)=O)C2=C(C=C3)C(C(C=CC=C5)=C5C(O4)=O)4C1=CC=C(OC(C)=O)C(CN(CC(OCOC(C)=O)=O)CC(OCOC(C)=O)=O)=C1O2

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

产品说明书 for Calcein AM

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参考文献 for Calcein AM

参考文献是支持产品生物活性的出版物。

Bakos et al (1996) Membrane topology and glycosylation of the human multidrug resistance-associated protein. J.Biol.Chem. 271 12322 PMID: 8647833

Lazarowski et al (1997) Direct demonstration of mechanically induced release of cellular UTP and its implication for uridine nucleotide receptor activation. J.Biol.Chem. 272 24328 PMID: 9305892

Kuehn et al (2011) Prostaglandin E2 activates and utilizes mTORC2 as a central signaling locus for the regulation of mast cell chemotaxis and mediator release. J.Biol.Chem. 286 391 PMID: 20980255

De Gendt et al (1996) The use of calcein acetomethylester (AM)-labelled polymorphonuclear cells in a polycarbonate filter chemotaxis assay. Clin.Chim.Acta. 249 189 PMID: 8737602


If you know of a relevant reference for Calcein AM, please let us know.

关键词: Calcein AM, Calcein AM supplier, CAS, 148504-34-1, fluorescent, probes, agents, general, cells, viability, chemotaxis, adhesion, multidrug, resistance, MDR, Fluorescent, Cell, Indicators, and, Sensors, Multidrug, Transporters, Viability, Stains, Dyes, Flow, Cytometry, 5119, Tocris Bioscience

5 篇 Calcein AM 的引用文献

引用文献是使用了 Tocris 产品的出版物。 Calcein AM 的部分引用包括:

Yannick D et al (2022) Protocol for serial organoid formation assay using primary colorectal cancer tissues to evaluate cancer stem cell activity. STAR Protoc 3 101218 PMID: 35265864

Walsh et al (2018) Loss of the mitochondrial kinase PINK1 does not alter platelet function. Sci Rep 8 14377 PMID: 30258205

Jiahn-Chun et al (2020) Interleukin-1β Enhances Umbilical Cord Mesenchymal Stem Cell Adhesion Ability on Human Umbilical Vein Endothelial Cells via LFA-1/ICAM-1 Interaction. Stem Cells Int 2019 7267142 PMID: 31949440

Guo et al (2018) Interleukin-1β induces CXCR3-mediated chemotaxis to promote umbilical cord mesenchymal stem cell transendothelial migration. Stem Cell Res Ther 9 281 PMID: 30359318


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cell viability assay.
By Karthik krishnamurthy on 10/24/2018
分析类型: In Vitro
种属: Human
细胞系/组织: motor neurons

For analyzing cellular toxicity in neurons

Neurons were treated with 50 uM glutamate for 1 hour. To assess the neuronal viability, neurons were incubated with calcein-AM (2 uM), and ethidium homodimer (4 uM) in HEPES buffer for 45-60 min at 37 degrees, rinsed with HEPES 4-5 times and examined under an epifluorescence microscope. This assay clearly distinguished live cells stained positive for calcein (green) from the dead cells stained positive for ethidium homodimer (red).

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Fluorescent Dyes and Probes Research Product Guide

Fluorescent Dyes and Probes Research Product Guide

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