A fusion reagent used to transfer beads and nanoparticles into the cytoplasm of living cells
Efficient incorporation of beads and particles with diameters in the nm to µm range
Superior fusion efficiency (up to 80-100%)
Fusion process completed within 1 - 20 minutes
Ready to use
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Magnetic µm-bead incorporation for magnetic tweezers experiments
Long-term live cell tracking
Cell purification assays using paramagnetic nm-beads
Incorporation of antibody-coupled particles for labeling, speckle microscopy, electron microscopy, etc.
Analysis of nanoparticle effects on cell behavior
After membrane fusion, the cells can immediately be used for further analysis. Multiple bead or single bead transfer is possible, depending on incubation time and bead concentration. Depending on your experimental needs, the fusion process can be monitored by fluorescence microscopy.
Note: The transfer of positively charged beads can affect fusion efficiency.
CHO cells fused with Fuse-It-Beads for 2 minutes with M-270 magnetic Dynabeads.
Principle of Membrane Fusion
The incorporation of small liposomal carriers into the plasma membrane of mammalian cells is the idea behind all of ibidi’s Fuse-It products. Liposomal carriers are able to attach and instantly fuse with plasma membranes in a physicochemical-driven manner. ibidi’s new Fuse-It reagents efficiently use this mechanism and fuse with mammalian cell surfaces immediately upon contact. Therefore, this novel technique makes the transfer of molecules independent of biological processes, such as endocytosis, pinocytosis, or specific receptor binding.
Reinhard Windoffer, Institute for Molecular and Cellular Anatomy (MOCA), University Hospital RWTH Aachen, Germany
"The incorporation of magnetic beads into cells for use in our magnetic tweezers experiments was extremely difficult and stressful for our cells. With Fuse-It-Beads, we can now easily perform the incorporation within a few minutes, making our experiments much easier and more reliable.”
Dr. Reinhard Windoffer Institute for Molecular and Cellular Anatomy (MOCA) University Hospital RWTH Aachen Germany