Calcein AM Assay Kit (Fluorometric) (ab228556)
Key features and details
- Assay type: Cell-based (quantitative)
- Detection method: Fluorescent
- Platform: Microplate reader
- Sample type: Adherent cells, Suspension cells
Overview
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Product name
Calcein AM Assay Kit (Fluorometric) -
Detection method
Fluorescent -
Sample type
Adherent cells, Suspension cells -
Assay type
Cell-based (quantitative) -
Product overview
Calcein AM Assay Kit ab228556 is a simple, extremely sensitive quantitative assay to measure the cell viability of adherent and suspension cells. It can detect as low as 50 viable cells in less than 30 minutes.
Calcein AM is a non-fluorescent, hydrophobic compound that easily penetrates intact and live cells.
During the Calcein AM assay, hydrolysis of Calcein AM by intracellular esterases produces a hydrophilic, strongly fluorescent compound that is retained in the cell cytoplasm and can be measured at Ex/Em = 485/530 nm. The measured fluorescence intensity is proportional to the number of viable cells.
The Calcein AM assay can be used for cell proliferation, cell viability, and cytotoxicity studies.
Review our cell health assays guide to learn more about our other cell viability, cytotoxicity and cell proliferation assay kits.
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Notes
This product is manufactured by BioVision, an Abcam company and was previously called K305 EZViable™ Calcein AM Cell Viability Assay Kit (Fluorometric). K305-1000 is the same size as the 1000 test size of ab228556.
Review the cell health assay guide to learn about more kits to perform a cell viability assay, cytotoxicity assay and cell proliferation assay.
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Platform
Microplate reader
Properties
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Storage instructions
Store at -20°C. Please refer to protocols. -
Components 1000 tests Assay Buffer XXVII 1 x 100ml Cell Dye II 2 vials
Associated products
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Related Products
Images
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Cell Viability Assay: Fibroblast cells were grown in DMEM supplemented with 10% FBS, harvested using trypsin and counted using Trypan blue and a hemocytometer. Cells were serially diluted in a clear cell culture plate and incubated for 30 minutes with Calcein AM at 37°C. After incubation, cells were lysed using Cell Lysis Buffer for 10 minutes at room temperature. Cell lysates were transferred into a 96-well white plate and fluorescence was measured. Inset graph is an expanded segment of the assay data at lower cell number per well.
Datasheets and documents
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Datasheet download
References (1)
ab228556 has been referenced in 1 publication.
- Su Y et al. Aptamer engineering exosomes loaded on biomimetic periosteum to promote angiogenesis and bone regeneration by targeting injured nerves via JNK3 MAPK pathway. Mater Today Bio 16:100434 (2022). PubMed: 36186848