PNExo™ Exosome-Onion(PNE-VO45)
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| Name | PNExo™ Exosome-Onion |
| Cat No. | PNE-VO45 |
| Source | Exosome derived from Onion |
| Product Overview | Plant exosomes are nanosized (30-150 nm) membrane vesicles that contain biomolecules. Plant-derived exosomes refer to naturally occurring nanoparticles derived from plants that contain bioactive molecules and proteins. These exosomes have been shown to have multiple benefits in a variety of applications, such as skincare, drug delivery, and biomedicine. Plant-derived exosomes have been found to possess antioxidant, anti-inflammatory, and anti-aging properties, making them an attractive option for the development of new and innovative therapies. Plant-derived natural substances are widely used as cosmeceutical materials because they exert beneficial effects on the human skin, such as antiaging, moisturizing, whitening, regeneration, and nutritional supply. Besides, they could delivery therapeutic compounds to target cells, potentially revolutionizing the way in which drugs are administered. Overall, plant-derived exosomes hold great promise for a wide range of applications in the fields of medicine and biotechnology. PNExo™ is focused on the production and delivery of high quality plant-derived exosomes products. Exosomes are important tools of intercellular communication with a variety of biological functions, including cell regeneration and immune regulation. PNExo™ products undergo a rigorous screening and purification process that guarantees their high purity and activity. Lyophilization is useful for a long-term storage at 4°C, and frozen liquid should be kept at -20°C to -80°C. Ultracentrifugation and precipitation techniques are mainly used in exosome Isolation. It had been reported that both methods yielded extracellular vesicles in the size range of exosomes and included apoproteins, which can be used in downstream analyses. Creative Biostructure PNExo™ exosome products guarantee higher purity and quality to meet our customer research. |
| Form | Lyophilized powder |
| Concentration | > 1x10^6 particles |
| Storage | Lyophilized powder store at 4 °C. Frozen liquid store at -20°C to -80°C. Recommended to avoid repeated freeze-and-thaw cycles. |
| Reconstitution | Reconstitute lyophilized exosome by adding deionized water for a desired final concentration. Centrifuge before opening to ensure exosomes are at bottom, resuspend exosomes by pipetting and/or vortex, please avoid bubbles. Centrifuge again and mix well for using. |
Creative Biostructure offers a wide range of plant exosome products and customized solutions, specializing in onion-derived exosome research. For detailed technical support or collaboration opportunities, please feel free to contact us. Our exosome services include, but are not limited to:
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Figure 1. Impact of onion-derived nanoparticles on nitric oxide production in LPS-treated RAW264 cells. The cells were incubated with two distinct concentrations of onion nanoparticles, 17 Kp and 200 Kp, for a duration of 24 hours prior to a subsequent 24-hour incubation with LPS at a concentration of 100 ng/mL. (A) The metabolic activity of the cells was evaluated utilizing the Cell Counting Kit-8, and the outcomes were depicted in terms of relative viability, normalized to the untreated control group. (B) The quantification of nitric oxide was conducted through the application of the Griess reagent system, with results expressed in terms of nitrate concentration. The presented values are the average ± standard error derived from triplicate experimental runs. Notable disparities from the group treated solely with LPS are denoted by asterisks, with * indicating a p-value less than 0.05 and ** signifying a p-value less than 0.01.
Figure 2. Effect of clathrin-dependent endocytosis inhibitor on intracellular uptake of onion-derived nanoparticles in RAW264 cells. These nanoparticles, categorized by their size into two groups (17 Kp and 200 Kp), were fluorescently tagged using the PKH26 dye. Prior to the introduction of the nanoparticles at concentrations of 400 μg/mL, the cells were subjected to a 1-hour pre-treatment with 10 mM of methyl-β-cyclodextrin (MβCD). The subsequent 2-hour incubation period facilitated the nanoparticles' interaction with the cells. The cellular nuclei were visualized post-staining with the Hoechst33342 fluorescent dye, and the cellular uptake was scrutinized under a confocal scanning laser microscope. Statistically significant variations in comparison to the groups treated with the 17 Kp or 200 Kp nanoparticles are denoted by asterisks, with a single asterisk representing a p-value below 0.05 and a double asterisk indicating a p-value below 0.01.