SCM144 Sigma-AldrichBrightCell™ MEMO® Photostable Media
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Panoramica
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| Description | |
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| Catalogue Number | SCM144 |
| Description | BrightCell™ MEMO® Photostable Media |
| Overview | BrightCell™ MEMO® photostable media is used as a replacement for DMEM prior to and during exposure to light during live cell imaging. MEMO® supplemented with SOS® during exposure to prolonged periods of blue light results in significantly higher levels of cell viability. Protocol Some of the phototoxic components present in standard media (but removed from MEMO/NEUMO) contribute to cellular proliferation. Consequently, MEMO/NEUMO should only be used during the phase of the experiment in which cells are exposed to prolonged periods of light. SOS, in contrast, supports cellular viability and proliferation equal to alternative (phototoxic) supplements and should be used continuously during cell maintenance. SOS® should be used to replace neuronal supplements, such as B-27®, if you are currently using these in your media. If you are presently using FBS, this can be harmful to cells under intensive light. Replacement of FBS with SOS® may help to support the growth of cells, especially when used in conjunction with cell line specific growth factors. Media Preparation 1. Thaw SOS at 37°C. SOS is supplied as a 25X concentrate and should be added to MEMO/NEUMO to a final concentration of 4%. Any liquid remaining should be aliquoted into working volumes and store at -20°C. Note: Avoid freeze-thawing of SOS® supplement more than twice. 2. Add additional components in an aseptic manner according to Table 1 in the userguide. 3. Once supplemented, the complete media is stable for 2 weeks when stored at 4°C. Cell Culture 1. Initially expand/maintain cells in the dark using Neurobasal supplemented with SOS. 2. The evening before exposure to prolonged periods of light, replace Neurobasal/SOS with pre-warmed MEMO/NEUMO and SOS. Cells will maintain viability for up to 3 days if required. a.Aliquot media to pre-heat, repetitive heating and cooling of bottles of media may cause precipitation. 3. Perform experiment requiring exposure to light. 4. Once exposure to light has been completed, remove the MEMO/NEUMO and SOS and replace with Neurobasal/SOS. BrightCell™ is a trademark of Merck KGaA. MEMO®, NEUMO® and SOS® are registered trademarks of Cell Guidance Systems LLC. Neurobasal® and B-27® are registered trademarks of Life Technologies. |
| Background Information | Experiments with live cultured cells, including fluorescence microscopy, optogenetics, and fluorescence activated cell sorting (FACS) often entail high levels or prolonged exposure to blue light. However, cell culture media and supplements contain components that are converted to toxic free radicals by light. In particular, DMEM (Dulbecco’s Modified Eagle Medium) and Neurobasal® medium, as well as cell culture supplements such as B-27®, SATO and NS21, can lead to significant perturbation of cellular behavior and marked increases in cell death. This phenomenon was recently highlight in the following nature publication: Surpassing light-induced cell damage in vitro with novel cell culture media. Nature Scientific Reports (Learn More!) The BrightCell photostable media system is cell culture media and supplements that have been reformulated with specific phototoxic components eliminated or replaced. The products allow prolonged exposure of cells to blue light while maintaining high levels of cell viability and functionality. Furthermore, BrightCell media products have very low levels of auto-fluorescence and photo-bleaching, dramatically improving the quality of data that can be obtained using fluorescent live cell imaging. |
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| Quality Level | MQ300 |
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| Application | Live cell imaging cell culture media (DMEM), 500ml |
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| Media Form | Liquid |
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| Material Size | 500ml |
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| Numero di catalogo | GTIN |
| SCM144 | 04054839445910 |
Documentation
Manuali d'uso
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| BrightCell¿ Photostable Media System |