Le prestigieux Salk Institute, fondé par le pionnier des vaccins Jonas Salk, a rédigé et publié un article scientifique qui fait l'effet d'une bombe...Cette protéine de pointe spike pourrait se fixer dans tous le corps et serait donc responsable à elle seule de beaucoup de symptômes tels que hyper tension hypo tension, perte de goût et d'odorat, problèmes cérébraux, problèmes neurologiques, maladies cardiaques, donc cette protéine spike n'est en aucun cas un virus !!! c'est une ARME BIOLOGIQUE et qui dit arme dit but recherché = DESTRUCTION !!! FAITES VOS PROPRES RECHERCHES MAIS RÉVEILLEZ VOUS !!! ?

It is done through a lipid nano system. To push the mRNA technology into places it was never meant to be. It was done to intentionally harm you. NOBODY HAS BEEN GIVEN INFORMED CONSENT. This extremely harmful additive was included on purpose. What I found on Magnetofaction: Magnetofection is a simple and highly efficient transfection method that uses magnetic fields to concentrate particles containing nucleic acid into the target cells. This method attempts to unite the advantages of the popular biochemical (cationic lipids or polymers) and physical (electroporation, gene gun) transfection methods in one system while excluding their inconveniences (low efficiency, toxicity). Magnetofection is commercialized by OZ Biosciences and is registered as a trademark. The magnetofection principle is to associate nucleic acids with cationic magnetic nanoparticles: these molecular complexes are then concentrated and transported into cells supported by an appropriate magnetic field. In this way, the magnetic force allows a very rapid concentration of the entire applied vector dose onto cells, so that 100% of the cells get in contact with a significant vector dose. Magnetofection has been adapted to all types of nucleic acids (DNA, siRNA, dsRNA, shRNA, mRNA, ODN), non viral transfection systems (transfection reagents) and viruses. It has been successfully tested on a broad range of cell lines, hard-to-transfect and primary cells. Several optimized and efficient magnetic nanopartciles formulations have been specifically developed for several types applications such as DNA, siRNA, and primary neuron transfection as well as viral applications. The magnetic nanoparticles are made of iron oxide, which is fully biodegradable, coated with specific cationic proprietary molecules varying upon the applications. Their association with the gene vectors (DNA, siRNA, ODN, virus, etc.) is achieved by salt-induced colloidal aggregation and electrostatic interaction. The magnetic particles are then concentrated on the target cells by the influence of an external magnetic field generated by magnets. The cellular uptake of the genetic material is accomplished by endocytosis and pinocytosis, two natural biological processes. Consequently, membrane architecture & structure stays intact, in contrast to other physical transfection methods that damage the cell membrane. The nucleic acids are then released into the cytoplasm by different mechanisms depending upon the formulation used: 1) is the proton sponge effect caused by cationic polymers coated on the nanoparticles that promote endosome osmotic swelling, disruption of the endosome membrane and intracellular release of DNA form, 2) is the destabilization of endosome by cationic lipids coated on the particles that release the nucleic acid into cells by flip-flop of cell negative lipids and charge neutralization and 3) is the usual viral infection mechanism when virus is used. Magnetofection works for primary cells and hard to transfect cells that are not dividing or slowly dividing, meaning that the genetic materials can go to the cell nucleus without cell division. Coupling magnetic nanoparticles to gene vectors of any kind results in a dramatic increase of the uptake of these vectors and consequently high transfection efficiency. The biodegradable cationic magnetic nanoparticles are not toxic at the recommended doses and even higher doses. Gene vectors / magnetic nanoparticles complexes are seen into cells after 10–15 minutes that is much faster than any other transfection method. After 24, 48 or 72 hours, most of the particles are localized in the cytoplasm, in vacuoles (membranes surrounded structure into cells) and occasionally in the nucleus.