ExoFlow-ONE EV Labeling Kit for Flow Cytometry (Garnet Far Red)

Product Description

• Directly detect EVs by specifically labeling internal EV components
• Accurately estimate the size of labeled EVs
• Ensure proper run-to-run calibration with the included size standards
• Learn more from a single sample by multiplexing with our range of spectrally separated ExoFlow-ONE dyes
• Achieve near single-vesicle visualization* with our proprietary ExoFlow-ONE dyes that deliver
  > High quantum efficiency
  > Negligible background signal when not bound to EVs

Finally, you can take full advantage of the power of flow-based methods for analyzing extracellular vesicles (EVs) with SBI’s exclusive ExoFlow-ONE Gemstone dyes. By specifically labeling internal EV components with one of these proprietary, high quantum efficiency dyes, you can achieve near single-vesicle resolution* for more powerful flow cytometry and FACS studies, and uncover greater insights into EV biology.

The ExoFlow-ONE Garnet Far Red Gemstone Dye Kit comes with enough labeling reagents for 25 reactions**. Each kit also includes 1.5 mL of silica bead size standards (110 nm – 1300 nm), two of which are fluorescent. The silica beads, sourced from Apogee Flow Systems, are specifically designed to produce a refractive index and light scattering patterns similar to biological particles, enabling more accurate estimation of EV particle size.

*Requires a specialized flow cytometry imager capable of high-resolution vesicle analysis (e.g. Amnis® ImageStreamX Mark II, Apogee Micro-PLUS).
**Each reaction is defined as 1 µL of working dye combined with 200 – 500 µg of EV protein resuspended in 500 µL of buffer.

Choose the right ExoFlow-ONE dye for your project

Supporting Data

Figure 1. The excellent spectral separation of ExoFlow-ONE dyes supports greater flexibility and enables more powerful multi-parametric flow experiments with EVs. We ran unlabeled EVs and EVs labeled with either Citrine Yellow ExoFlow-ONE, Garnet Far Red ExoFlow-ONE, or Ruby Red ExoFlow-ONE on a BD® LSR II Flow Cytometer, and plotted the signals detected in the phycoerythin (PE) channel versus the Alexa 700 channel. The clear spectral separation of all four EV populations demonstrates multiplexing capabilities capabilities of ExoFlow-ONE dyes.