PNExo™ Exosome-Carrot(PNE-VC16)
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| Name | PNExo™ Exosome-Carrot |
| Cat No. | PNE-VC16 |
| Source | Exosome derived from Carrots |
| 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. |
Carrot exosomes, rich in beneficial compounds like carotenoids and vitamins, show potential in health applications, particularly in reducing oxidative stress and cellular damage. They may offer therapeutic benefits for conditions such as myocardial infarction and Parkinson's Disease. Creative Biostructure specializes in advancing the study and application of these plant-based exosomes, offering tailored research solutions. For inquiries on customized carrot exosome research, reach out to us.
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Isolation of carrot-derived nanovesicles and their antioxidant effects on cardiac and neural cells. (Kim D K, et al., 2021)
Figure 1. The impact of Carex on antioxidant and apoptosis activities in H9C2 cardiac myoblasts.
(A) H9C2 cells were exposed to a concentration of 1 × 10^11 particles/mL of Carex to induce oxidative stress via H2O2. The levels of reactive oxygen species (ROS) within the cells were visualized in green, and the cell nuclei were counterstained in blue using the fluorescent dyes H2DCFDA and Hoechst 33342, respectively. The images were captured under a fluorescence microscope, with scale bars representing 100 micrometers.
(B) The cells were treated with varying doses of Carex for 24 hours prior to H2O2 exposure. The WST-1 assay was employed to determine the cells' viability.
(C) The effect of Carex on the inhibition of Caspase-3 activity in H9C2 cells was assessed.
(D–F) The relative expression levels of Nrf-2 (D), HO-1 (E), and NQO-1 (F) mRNA were quantified using reverse transcription polymerase chain reaction (RT-PCR) analysis.
(G) Protein levels of Nrf-2 and HO-1 were analyzed by Western blot, with GAPDH serving as a loading control. Data are presented as mean values with standard deviation (SD). Statistical significance is indicated by asterisks (* for p < 0.05, *** for p < 0.001; n = 3).
Figure 2. Carex-mediated reduction of oxidative and apoptotic impacts in SH-SY5Y neuroblastoma cells.
(A) The influence of varying concentrations of Carex on cell population and its potential to induce cell death was quantitatively assessed.
(B) The capacity of Carex to counteract apoptosis in SH-SY5Y cells exposed to 6-OHDA was evaluated through the WST-1 viability assay.
(C) The suppression of caspase-3 enzymatic activity in SH-SY5Y cells given a Carex particle concentration of 1 × 10^11/mL was observed.
(D–F) The relative transcript levels of Nrf-2, HO-1, and NQO-1, as determined by reverse transcription-polymerase chain reaction (RT-PCR), were analyzed in SH-SY5Y cells following 6-OHDA treatment. Data are presented as mean values with standard deviations (* indicates p < 0.05, ** p < 0.01, *** p < 0.001; replicates = 3).