Vesi-SEC
Isolate and purify samples before analytics and functional assays.
Isolate and purify samples before analytics and functional assays.
Specific staining of lipid bilayers in exosomes, liposomes and viruses.
Extracellular vesicle and liposome reference materials for flow cytometry and other analytical methods
Stabilisation & storage buffer for extracellular vesicles
Once EVs have been isolated, they can be stabilised for weeks to years using Vesi-Safe, a PBS-based buffer contains ingredients that prevent vesicle loss to adhesion to plastics. Finally, in order to make EVs detectable by fluorescence-capable technologies, these can be specifically and permanently stained with Vesi-LMB probes, which specifically intercalate in the membrane lipid bilayer. Excess dye is swiftly removed by Vesi-SEC Micro spin columns. Positive controls and calibration of these experiments can be performed using the Vesi-Ref family of reference materials.
Size-exclusion chromatography is vastly superior to standard filtration, but in its traditional form, it is labour-intensive, time consuming and dilutive, making it difficult to implement in formulation development operations. Vesi-SEC spin columns are only fast, but also highly scalable, with their format compatible with standards centrifuges, allowing capacities of over 100 columns simultaneously. Unbound material is immobilised on the column’s stationary phase and the purified LNP or liposome sample recovered in just 1 minute.
Exploring this frontier requires more than just advanced analytical devices, it also demands the right reagents and carefully designed protocols to capture the correct phenomena and avoid misleading artifacts. Only by combining precision instrumentation with purpose-built staining, stabilisation, and reference tools can researchers draw reliable conclusions that expand scientific understanding. Vesiculab understands these requirements, and develops solutions that help deepening our knowledge of fundamental biological processes and accelerates the translation of discoveries into diagnostics and therapies.
Nanoparticle Analysis
Dynamic Light Scattering
Nano-Flow Cytometry
Interferometric Light Microscopy
Transmission Electron Microscopy
Resistive Pulse Sensing
Single Particle Interferometric Reflective Image Sensing
Direct Stochastic Optical Reconstruction Microscopy