HQExo™ Exosome-Potato(Exo-PDELN04)
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| Name | HQExo™ Exosome-Potato |
| Cat No. | Exo-PDELN04 |
| Source | Exosome derived from Potato |
| Product Overview | Exosomes are nanosized vesicles (30-160 nm) secreted by exocytosis by most cell types and contain specifical cargos, such as RNAs, lipids, and proteins. The cargos amount and composition of exosomes depend on the cell type from which they are released, which making them useful for biomarker discovery and functional characterization. Exosomes have been isolated plant, which comprises various bioactive biomolecules. As an alternative cell-free therapeutic approach, plant drived exosome particles have the enormous potential in drug delivery system. HQExo™ standard exosomes could use as positive controls for exosome isolation and functional research, such as ELISA, FACS, WB. 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, which can be used in downstream analyses. Nanoparticles Tracking Analysis (NTA) is used for measuring exosome particles concentration. Creative Biostructure standard exosome products guarantee higher purity and quality to meet our customer research. |
| Form | Lyophilized powder/ frozen liquid |
| Concentration | >1x10^8 particles |
| Storage | Store at -20°C or colder. Recommend 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 specialized services on potato-derived exosomes. These exosomes have similar properties to those from other sources and are being studied for their potential in skincare and wound healing. Our team has the expertise and resources to support research in this area. If you're interested, please get in touch to discuss how we can help with your project.
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Figure 1. The impact of potato exosomes (ExoPs) on the survival of HaCaT cells was evaluated. (A) The WST-1 assay was utilized to determine the comparative cell viability, with untreated cells as the control. The viability ratio is expressed as a percentage, with ascorbic acid (AA) serving as a comparative benchmark. (B) The capacity of ExoPs to neutralize hydrogen peroxide (H2O2) was assessed by exposing HaCaT cells to H2O2 and subsequently introducing varying levels of ExoPs. (C) The ExoPs' ability to quench DPPH free radicals was examined using the standard antioxidant AA. A concentration range of 0 to 4 mg/ml of ExoPs was mixed with DPPH, incubated in darkness at room temperature for 30 minutes, and then the absorbance was recorded at 517 nm via spectrophotometry. (D) The influence of ExoPs on HaCaT cells subjected to ultraviolet B (UVB) radiation was studied, with cells being pre-treated or post-treated with ExoPs.
Figure 2. Mechanism of UVB photodamage prevention and mitigation by ExoPs. (A) RT-PCR was used to validate the concentration-dependent inhibition of UVB-induced MMP1, IL6, and TNF-α expression by ExoPs in HaCaT keratinocyte cells. (B) PCR analysis of MMPs, cytokine genes, and GSTA4 expression levels when HaCaT cells were treated with ExoPs both prior to and following UVB exposure. (C) Impact of ExoPs on collagen production in HaCaT cells subjected to UVB irradiation.