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MitoStep + Apoptosis Detection Kit
MitoStep + PE Apoptosis Detection Kit, FITC/PE
Artikelnummer
IMSKMAPE-100T
Verpackungseinheit
100 Tests
Hersteller
Immunostep
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Conjugate: PE.
Storage Buffer: DilC1(5), 500 μlof 10μM in DMSO + The reagent is provided in aqueous buffered solution containing protein stabilizer, and ≤0.09% sodium azide (NaN3).
Recommended Usage: This reagent is intended for RUO in the identification of apoptotic cells. For flow cytometric staining, the suggested use of this reagent is 5 µl per 1 - million cells in a 100 µl volume Buffer.
Description: Membrane potential is generated and maintained by concentration gradients of ions such as sodium, potassium, chloride, and hydrogen. Mitochondrial drives the accumulation in mitochondria of cationic dyes such as cyanines, and the mitochondrial is reduced when energy metabolism is disrupted, notably in apoptosis. Changes in the mitochondrial potential have been described during necrosis, cell cycle and apoptosis. Mitochondrial uptake of dye is a possible source of fluorescence variance. Flow cytometry can be used to estimate membrane potential in eukaryotic cells. Methods using cyanines dyes can detect changes in membrane potential. Immunostep MitoStep uses a cationic dye DilC1(5) (1,1).
Membrane potential is generated and maintained by concentration gradients of ions such as sodium, potassium, chloride, and hydrogen. Mitochondrial drives the accumulation in mitochondria of cationic dyes such as cyanines, and the mitochondrial is reduced when energy metabolism is disrupted, notably in apoptosis. Changes in the mitochondrial potential have been described during necrosis, cell cycle and apoptosis. Mitochondrial uptake of dye is a possible source of fluorescence variance. Flow cytometry can be used to estimate membrane potential in eukaryotic cells. Methods using cyanines dyes can detect changes in membrane potential. Immunostep MitoStep uses a cationic dye DilC1(5) (1,1)
Storage Buffer: DilC1(5), 500 μlof 10μM in DMSO + The reagent is provided in aqueous buffered solution containing protein stabilizer, and ≤0.09% sodium azide (NaN3).
Recommended Usage: This reagent is intended for RUO in the identification of apoptotic cells. For flow cytometric staining, the suggested use of this reagent is 5 µl per 1 - million cells in a 100 µl volume Buffer.
Description: Membrane potential is generated and maintained by concentration gradients of ions such as sodium, potassium, chloride, and hydrogen. Mitochondrial drives the accumulation in mitochondria of cationic dyes such as cyanines, and the mitochondrial is reduced when energy metabolism is disrupted, notably in apoptosis. Changes in the mitochondrial potential have been described during necrosis, cell cycle and apoptosis. Mitochondrial uptake of dye is a possible source of fluorescence variance. Flow cytometry can be used to estimate membrane potential in eukaryotic cells. Methods using cyanines dyes can detect changes in membrane potential. Immunostep MitoStep uses a cationic dye DilC1(5) (1,1).
Membrane potential is generated and maintained by concentration gradients of ions such as sodium, potassium, chloride, and hydrogen. Mitochondrial drives the accumulation in mitochondria of cationic dyes such as cyanines, and the mitochondrial is reduced when energy metabolism is disrupted, notably in apoptosis. Changes in the mitochondrial potential have been described during necrosis, cell cycle and apoptosis. Mitochondrial uptake of dye is a possible source of fluorescence variance. Flow cytometry can be used to estimate membrane potential in eukaryotic cells. Methods using cyanines dyes can detect changes in membrane potential. Immunostep MitoStep uses a cationic dye DilC1(5) (1,1)
Immer für Sie da
Gernot Ensinger, M.Sc.
