- 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.
|ExMax/EmMax||750/780 nm (infrared)|
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.