Overview
Delivering ELISA-based exosome quantitation ULTRA fast
Improving on our popular ExoELISA™ Kits, the ExoELISA-ULTRA CD63 Kit increases the sensitivity of exosome detection—as low as 1 µg protein equivalent—while shortening the total assay time to only 4 hours.
Currently configured for detection of CD63, a widely recognized and popular exosomal marker1, ExoELISA-ULTRA CD63 is based on an ultra-sensitive, direct capture, colorimetric ELISA assay that is compatible with nearly all biofluids. The ExoELISA-ULTRA CD63 Kit comes with an internal standard calibrated to exosomes from a range of biofluids. Calibration is achieved by NanoSight analysis and enables quantitation of exosomes carrying CD63 in your target samples. One ExoELISA-ULTRA CD63 Kit contains all of the necessary reagents (including assay plate) to perform up to 96 reactions.
- Sensitive—detect as little as 1 µg protein equivalent
- Fast—complete in less than 4-hours—no more overnight incubation
- Flexible—compatible with all major exosome isolation methods (e.g. ExoQuick®, ultracentrifugation, ultrafiltration, and immunoaffinity capture) from human samples
- Quantitative—calibrated internal standards enable quantitation of exosomes carrying CD63
- Sample-saving—requires significantly less sample than our standard ExoELISA Kit, leaving more for other downstream applications
Choose the exosome quantitation method that’s best for your studies
ExoELISA-ULTRA CD63ExoELISA-ULTRA CD81 | ExoELISA CD9ExoELISA CD63ExoELISA CD81 | EXOCET | FluoroCet | |
---|---|---|---|---|
Use | For fast and sensitive antibody-based quantitation of exosomes | For sensitive quantitation of exosomes when time and input sample are not limiting | For fast quantitation of extracellular vesicles with moderate sample input requirements | For the most sensitive quantitation of extracellular vesicles with very low sample input requirements |
Detection method | Antibody | Antibody | Enzymatic | Enzymatic |
Quantitation chemistry | Enzymatic (HRP) | Enzymatic (HRP) | Colorimetric | Fluorescent |
Total protocol time | 4 hours (no overnight incubation) | 24 hours | 20 min | 60 min |
Input sample amount (protein equivalent) | 1 – 200 µg | >500 µg | 50 µg | <1>1> |
Learn More | ExoELISA-ULTRA CD63 ExoELISA-ULTRA CD81 | ExoELISA CD9ExoELISA CD63ExoELISA CD81 | EXOCET | FluoroCet |
REFERENCES
- Kowal, J., et al. Proteomic comparison defines novel markers to characterize heterogeneous populations of extracellular vesicle subtypes. Proc Natl Acad Sci U S A. 2016. February 23. 113(8): E968–E977. PMCID: PMC4776515.
Supporting Data
The standard curve for ExoELISA-ULTRA CD63 shows robust linearity down to ~1 x 109 exosomes.
Resources
Citations
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- Kim, JH, Lee, CH & Lee, SW. (2019) Exosomal Transmission of MicroRNA from HCV Replicating Cells Stimulates Transdifferentiation in Hepatic Stellate Cells. Mol Ther Nucleic Acids.2019 Mar 1; 14:483-497. PM ID:30753992
- Capello, M, et al. (2019) Exosomes harbor B cell targets in pancreatic adenocarcinoma and exert decoy function against complement-mediated cytotoxicity. Nat Commun.2019 Jan 16; 10(1):254. PM ID:30651550
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- Baryeh, K. (2019) Development of Quantitative Lateral Flow Strip Biosensors for the Detection of Cancer Biomarkers. Thesis.;. Link:Thesis
- Cheema, AK, et al. (2018) Plasma Derived Exosomal Biomarkers of Exposure to Ionizing Radiation in Nonhuman Primates. Int J Mol Sci.2018 Nov 1; 19(11). PM ID:30388807
- La Shu, S, et al. (2018) Metabolic reprogramming of stromal fibroblasts by melanoma exosome microRNA favours a pre-metastatic microenvironment. Sci Rep.2018 Aug 27; 8(1):12905. PM ID:30150674
- Ruiz-de-León, MJ, et al. (2018) Lower expression of plasma-derived exosome miR-21 levels in HIV-1 elite controllers with decreasing CD4 T cell count. J Microbiol Immunol Infect.2018 Aug 24;. PM ID:30193823
- Lin, M, et al. (2018) Exosomal neutral sphingomyelinase 1 suppresses hepatocellular carcinoma via decreasing the ratio of sphingomyelin/ceramide. FEBS J..2018 Aug 14;. PM ID:30106227
- Zhou, Y, et al. (2018) Exosomes from Endothelial Progenitor Cells Improve the Outcome of a Murine Model of Sepsis. Mol. Ther..2018 Feb 27;. PM ID:29599080