The number of 'tests' is dependent upon the culture vessel and will have to be determined by the end user. Chamber slides or coverslips will require less volume that t-flasks or culture dishes. As per instructions, the prepared 1mM stock solution is diluted to a working concentration of 1 µM prior to applying to cells. Please see the link below to review these instructions and a general protocol provided in the product datasheet:
https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/277/500/sct210-35nmolds.pdf
Seleccione un Tamaño
| A ustedes/SKU | Disponibilidad | Precio |
|---|---|---|
35 nmol | Comprobar disponibilidad del carrito | $198.00 |
175 nmol | Comprobar disponibilidad del carrito | $710.00 |
Acerca de este artículo
$198.00
form
lyophilized
application(s)
cell analysis
detection method
fluorometric
General description
Disclaimer
1 of 1
Este artículo | |||
|---|---|---|---|
| form lyophilized | form - | form - | form lyophilized |
| application(s) cell analysis | application(s) - | application(s) - | application(s) cell analysis |
| detection method fluorometric | detection method fluorometric | detection method fluorometric | detection method fluorometric |
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How many tests can be carried out using the 35 nmol package please?
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Can this kit be used for suspension cells?
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Yes, this product is suitable for use with suspension cells.
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Is it possible to store SCT210 after reconstitution?
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The available datasheet for SCT210 provides guidance in the Reagent Preparation section, stating, "Use neutral buffer or culture medium for dilution of the DMSO solution and use immediately upon dilution. The dye could be oxidized in acidic solutions." However, there are no recommendations or data suggesting that the solutions are stable when stored. It's important to note that the package is shipped in single-use vials.
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Is it possible to detect SCT210 FerroOrange by flow cytometry?
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The website indicates an excitation wavelength of 542 nm and an emission wavelength of 572 nm for the SCT210 FerroOrange. The product is claimed to be suitable for live cell imaging, which typically implies the use of a confocal microscope. However, given that this is a fluorescent dye, it seems reasonable to consider that the staining could be assessed using a flow cytometer. There is currently no available data documenting its use on a flow cytometer. To use it on a flow cytometer, the cells would need to be in a single cell suspension. Additionally, it is expected that the cells could be visualized using a fluorescent microscope.
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What cells can be used as a positive control for SCT210 (BioTracker™ FerroOrange Live Cell Dye)?
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The HepG2 cell line is recommended as a positive control for SCT210 (BioTracker™ FerroOrange Live Cell Dye).
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