$245.00 – $475.00
- Additional information
- ASSAY PRINCIPLE
- Readable Documents
- Kit contents and storage
- Cell Permeable, Easy One Color Assay for Flow Cytometry.
- Can be used with both suspension and monolayer adherent cell lines.
- Adaptable for High Throughput format.
- Compatible with other antibodies or stains. For example flourescent protein expression vectors.
- Applications – Flow Cytometry.
Cell Technology’s Mito Flow assay utilizes a cationic dye to visualize mitochondrial membrane potential (5-7). The Mito Flow reagent is a cell permeable cationic dye that has a strong fluorescent signal and exhibits low membrane potential independent (non specific) binding and toxicity. In healthy cells the Mito Flow reagent is accumulated by the mitochondria in proportion to the DeltaPsi (membrane potential). In most cell lines, accumulation of the Mito Flow reagent in the mitochondria results in a higher fluorescence intensity. In apoptotic cells, where the mitochondrial membrane potential is compromised, the Mito Flow reagent does not get accumulated in the mitochondria and these cells exhibit a lower fluorescence signal.
Figure 1. Jurkat cells were stimulated with DMSO for 3 hours. Cells were then stained by Mito Flow and analyzed by Flow Cytometry
Figure 1. Jurkat cells were stimulated with Staurosporine for 3 hours. Cells were then stained by Mito Flow and analyzed by Flow Cytometry
|Protocol||Mito Flo Protocol.pdf|
|Datasheet||Mito Flo Datasheet.pdf|
|msds||msds Mito Flo.pdf|
Kit contents and storage
|Part # 4004||Vial of Mito Flow Dye||2-8°C|
|Part # 3004||10X Dilution Buffer||2-8°C|
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|Luo, X., Budihardio, I., Zou, H., Slaughter, C., and Wang, X. Bid, a Bcl-2 interacting protein, mediates cytochrome c release from mitochondria in response to activation of cell surface death receptors. Cell 94: 481-490 (1998).|
|Ehrenberg B, Montana V, Wei MD, Wuskell JP, Loew LM. Membrane potential can be determined in individual cells from the nernstian distribution of cationic dyes. Biophys J. 1988 May;53(5):785-94.|
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|Russell C. Scaduto, Jr. and Lee W. Grotyohann. Measurement of mitochondrial membrane potential using fluorescent rhodamine derivatives. Biophys J. 1999 Jan;76(1 Pt 1):469-77.|
|Rajagopal A, Pant AC, Simon SM, Chen Y. In vivo analysis of human multidrug resistance protein 1 (MRP1) activity using transient expression of fluorescently tagged MRP1. Cancer Res. 2002 Jan 15;62(2):391-6.|
|Protective effects of veskamide, enferamide, becatamide, and oretamide on H2O2-induced apoptosis of PC-12 cells||http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B7GVW-529SW55-7&_user=10&_coverDate=03%2F05%2F2011&_rdoc=1&_fmt=high&_orig=gateway&_origin=gateway&_sort=d&_docanchor=&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=42a1e1b8c7f5c7ef2a670de8c3eab374&searchtype=a||Jae B Park||Phytomedicine||March 2011 – doi:10.1016/j.phymed.2011.01.025|