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DOI: 10.3791/67439-v
This protocol aims to isolate and purify skeletal muscle interstitial extracellular vesicles (SkM-EVs) from rodent muscle tissues using mechanical detachment, enzymatic dissociation, filtration, and differential ultracentrifugation. The isolated SkM-EVs provide insights into muscle homeostasis and diseases, offering potential applications as diagnostic biomarkers or therapeutic vehicles.
This protocol aims to isolate and purify skeletal muscle interstitial extracellular vesicles (SkM-EVs) from rodent muscle tissues through mechanical detachment, enzymatic dissociation, filtration, and differential ultracentrifugation. It demonstrates consistency and reliability. The isolated SkM-EVs provide insights into muscle homeostasis and diseases, with potential applications as diagnostic biomarkers or therapeutic vehicles.
This protocol aims to isolate and purify skeletal muscle interstitial extracellular vesicles in rodent muscle tissues. This extracellular vesicle will provide invaluable insights into the muscle human status disease mechanism with potential application as diagnostic biomarkers and therapeutical vehicles. This standardized protocol will enable the analysis and the comparison of characteristic of skeleton muscle derived EV across different muscle samples, including the yield, size, cargo composition and function.
These results will advance our understanding of their roles in various physiologic and pathological processes, and will also facilitate the application of these EVs as diagnostic biomarkers. Our laboratory will focus on reliably producing high purity and high-yield skeletal muscle interstitial extracellular vesicles in an efficient and time effective manner. We aim to explore their pathological role and therapeutic potential, particularly in the context of neuromuscular disorders.
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