Dojindo,PlasMem鲜红色/100/P505

质膜 (PM) 由将细胞内环境与细胞外空间隔开的脂质双层组成。 因此，PM 在许多细胞行为中起着核心作用，例如细胞迁移、细胞伸展和信号级联。 此外，PM功能障碍是一个重要的生物标志物，因为它与细胞状态有关，并与许多疾病有关。

Dojindo 的 PlasMem Bright 染料克服了这些限制。 PlasMem Bright 染料设计用于染色 PM 超过一天。 此外，与其他市售染料相比，PlasMem Bright 染料更易溶于水，并且可以用培养基稀释。 PlasMem Bright 染料提供两种不同的颜色选择（绿色和红色），并作为即用型 DMSO 溶液提供。 使用生长培养基或 HBSS 通过单一稀释步骤即可轻松制备工作溶液。

For more information on PlasMem Bright Dyes, please refer to the publication below:Takahashi, M. et al., “Amphipathic Fluorescent Dyes for Sensitive and Long-Term Monitoring of Plasma Membranes“ bioRxiv, 2020, doi: https://doi.org/10.1101/2020.11.16.379206

 

The general number of usable assays per 100 ul35 mm dish x 10μ-Slide 8 well x 10

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Low toxicity, No washing, and High retentivity

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High retentivity on plasma membrane

HeLa cells stained with each plasma membrane staining reagent were incubated for 24 hrs and each the resulting fluorescent image was compared. PlasMem Bright series had higher retentivity on plasma membrane than other products.

 

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Clear visualization of plasma membrane

Observe morphology of neuron (differentiated SH-SY5Y cells) and localization of mitochondria in axon.

Experimental Example: Mitochondrial detection in neuroblast (SH-SY5Y cells)

The neuroblasts SH-SY5Y cells were stained with PlasMem Bright Green (green), MitoBright LT Red (red) and Hoechst 33342 (blue), and 3D images were obtained with a confocal fluorescence microscope.

 

<Detection Condition>Plasma Membrane (PlasMem Bright Green, green): Ex. 488 nm / Em. 500 – 560 nmMitochondria (MitoBright LT Red, red): Ex. 561 nm / Em. 560 – 620 nmNuclear (Hoechst 33342, blue): Ex. 405 nm / Em. 400 – 450 nm

<Protocol>(1) Wash SH-SY5Y cells with HBSS(2) Add PlasMem Bright Green (diluted 200 times), Hoechst 33342 (final concentration: 5 µg / ml) and MitoBright LT Red (final concentration: 0.1 µmol / l) prepared in the medium.(3) Incubate for 10 minutes(4) Wash the cells twice with HBSS(5) Observation with a fluorescence microscope

<Detection conditions>Plasma Membrane (PlasMem Bright Green, green): Ex. 488 nm / Em. 500 –560 nmExosome (ExoSparkler Exosome Membrane Labeling Kit-Red, red): Ex. 561 nm / Em. 560 –620 nm

<Protocol>(1) HeLa cells and incubate for 24 hours(2) Remove the supernatant and add PlasMem Bright Green (100-fold dilution) prepared in the medium.(3) Incubate for 10 minutes(4) Wash the cells 3 times with HBSS(5) Add 175 μl of MEM medium and 25 ul of Exosome solution stained with ExoSparkler Exosome Membrane Labeling Kit-Red.(6) Incubate overnight in a CO2 incubator(For immobilization) Wash cells twice with HBSS, add 4% PFA, incubate for 15 minutes, then wash cells twice with HBSS(7) Observed with a confocal laser scanning microscope

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Experimental example: Time-lapse imaging of brain-derived mouse neuroblastoma (N1E-115 cells)

Time-lapse imaging of N1E-115 cells stained with PlasMem Bright Green diluted 200-fold in medium for 30 min.

 

<Detection conditions>・ Cells: N1E-115 cells (brain-derived mouse neuroblastoma)・ Medium: 5% FBS, 1% glutamine-containing D-MEM (Low-glucose)・ Culture equipment: 35 mm glass bottom dish・ Imaging equipment: Fluorescence microscope with incubator・ Shooting time: 1 hour, shooting interval: 2 minutes

Data was kindly provided from Dr. K Fukui, Shibaura Institute of Technology.