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CBA026  InnoCyte™ ECM Cell Adhesion Assay, Galectin-1/Galectin-3

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31 May 2012

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Product number Qty/Pk Quantity Price
CBA026-1KIT  1 kit  loading
Prices are subject to change without notice.
The InnoCyte™ Cell Adhesion Assay, Galectin-1/Galectin-3 is designed for the determination of the relative attachment of adherent cell lines to galectin-1 and galectin-3, for evaluation of cell adhesion receptors, and for assessment of inhibitory or stimulatory substances for cell attachment. The kit is supplied with a 96-well strip plate coated with galectin-1 and galectin-3. Cells are seeded in the coated wells and incubated at +37°C. Following incubation, the wells are washed briefly and attached cells are labeled the green fluorescent dye, calcein-AM. BSA-coated wells serve as a negative control and poly-L-lysine-coated wells serve as a positive control for general attachment. Relative cell attachment is assessed using a fluorescence plate reader.

96-well tissue culture plate coated with Galectin-1/Galectin-3
Assay is quick-can be performed in 2.5 h
Adherent cells are labeled with calcein-AM
Relative cell attachment is assessed using a fluorescence plate reader


Product information
Format 96-well plate
Form 72 Tests (36 Gal-1 and 36 Gal-3)
Detection method Fluorometric
Protect from Light Yes
Avoid freeze/thaw Yes
Assay time 2.5 h
Sample type Adherent cultured cells
Kit contains Coated 96-Well Plates, Fluorescent Dye, D-PBS, and a user protocol.
Store and ship information
Storage +2°C to +8°C
Ship Blue Ice Only
Multiple Toxicity Values, refer to MSDS
Data

~40,000 cells were added to wells coated with galectin-1, galectin-3, and BSA and incubated for 1.5 h at 37°C in the presence of 6% CO<sub>2</sub>. Cells were washed gently with D-PBS and labeled with Calcein-AM for 1 h at 37°C in the presence of 6% CO<sub>2</sub>. Fluorescence was measured as indicated in the Detailed Protocol. HT-1080 cells displayed appreciable binding to poly-L-lysine, which served as a positive control (data not shown).

© Merck KGaA, Darmstadt, Germany, 2012


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