MAGNETOFECTION (2019)
"Improving Magnetofection of Magnetic Polyethylenimine Nanoparticles into MG-63 Osteoblasts Using a Novel Uniform Magnetic Field (2019): This study aimed to improve the magnetofection of MG-63 osteoblasts by integrating the use of a novel uniform magnetic field with low molecular weight polyethylenimine modified superparamagnetic iron oxide nanoparticles (PEI-SPIO-NPs). The excellent characteristics of PEI-SPIO-NPs such as size, zeta potential, the pDNA binding and protective ability were determined to be suitable for gene delivery. The novel uniform magnetic field enabled polyethylenimine-modified superparamagnetic iron oxide nanoparticles/pDNA complexes (PEI-SPIO-NPs/pDNA complexes) to rapidly and uniformly distribute on the surface of MG-63 cells, averting local transfection and decreasing disruption of the membrane caused by the centralization of positively charged PEI-SPIO-NPs, thereby increasing the effective coverage of magnetic gene carriers during transfection, and improving magnetofection efficiency."
https://pubmed.ncbi.nlm.nih.gov/30874913/

MAGNETOFECTION (2011)
"Magnetofection is an efficient new physical gene transfection technology. Despite its effective gene delivery capability, till now relatively little work has been conducted on the mechanism of magnetofection, especially the intracellular fates of the components of magnetofectins and their effects on magnetofection. In this study, we investigated the mechanism of magnetofection using magnetofectins that were prepared via electrostatic self-assembly of the three components: polyethyleneimine (PEI)-coated magnetic nanoparticles (MNPs-PEI), plasmid DNA (pDNA) and PEI in the free form (free PEI). TEM observation and agarose gel electrophoresis assays have indicated MNPs play the role of driving magnetofectins to the cell surface without entering into the nucleus."
https://pubmed.ncbi.nlm.nih.gov/21807084/

MAGNETOFECTION AS VACCINE DELIVERY SYSTEM (2014) 🧲💉🩸

"The efficiency of delivery of DNA vaccines is often relatively low compared to protein vaccines. The use of superparamagnetic iron oxide nanoparticles (SPIONs) to deliver genes via magnetofection shows promise in improving the efficiency of gene delivery both in vitro and in vivo. In particular, the duration for gene transfection especially for in vitro application can be significantly reduced by magnetofection compared to the time required to achieve high gene transfection with standard protocols. SPIONs that have been rendered stable in physiological conditions can be used as both therapeutic and diagnostic agents due to their unique magnetic characteristics. Valuable features of iron oxide nanoparticles in bioapplications include a tight control over their size distribution, magnetic properties of these particles, and the ability to carry particular biomolecules to specific targets. The internalization and half-life of the particles within the body depend upon the method of synthesis. Numerous synthesis methods have been used to produce magnetic nanoparticles for bioapplications with different sizes and surface charges. The most common method for synthesizing nanometer-sized magnetite Fe3O4 particles in solution is by chemical coprecipitation of iron salts. The coprecipitation method is an effective technique for preparing a stable aqueous dispersions of iron oxide nanoparticles. We describe the production of Fe3O4-based SPIONs with high magnetization values (70 emu/g) under 15 kOe of the applied magnetic field at room temperature, with 0.01 emu/g remanence via a coprecipitation method in the presence of trisodium citrate as a stabilizer. Naked SPIONs often lack sufficient stability, hydrophilicity, and the capacity to be functionalized. In order to overcome these limitations, polycationic polymer was anchored on the surface of freshly prepared SPIONs by a direct electrostatic attraction between the negatively charged SPIONs (due to the presence of carboxylic groups) and the positively charged polymer. Polyethylenimine was chosen to modify the surface of SPIONs to assist the delivery of plasmid DNA into mammalian cells due to the polymer's extensive buffering capacity through the "proton sponge" effect."
https://pubmed.ncbi.nlm.nih.gov/24715289/

magnetofection_2_4.pdf

Cover of pdf above

"#Magnetofection is a novel, simple and highly efficient method to transfect cells in culture. #CombiMAGis a #magnetic particle preparation designed to be combined with any commercially available transfection reagent such as polycations and #lipids"
https://web.archive.org/web/20191231104325/http://www.chemicell.com:80/products/magnetofection/docs/magnetofection_2_4.pdf#

MY EDUCATED GUESS: THE INJECTIONS ARE MAGNETIC BECAUSE OF MAGNETOFECTION. WHAT ARE THE LONG TERM EFFECTS ON THE HUMAN BODY? MANUAL FROM MANUFACTURER LINK & PDF ABOVE. THEY DID NOT TELL US DID THEY? 🧲💉🩸

They lied about EVERYTHING so far but somehow they would be truthful about what's in the injections? Why? That's not how they work. I would suggest the opposite: the whole operation began with the ingredients of the injections and the lies around them. The vaccine ingredients are most likely the ORIGIN of the big lie. It's where the Minotaur lives.

Dr Mike Yeadon Interviewed by Frank Gaffney on “Securing America”.
Please be patient as the video seemed to take some time to begin.
Though this is a boutique broadcaster, Gaffney has high listenership in Washington, having had a role in the Reagan administration.

Robin,
Long form podcast interview by Frank Gaffney, who was a member of President Ronald Reagan’s foreign policy administration.
Please share widely. Thank you.
Dr Mike Yeadon

Piers Corbyn swings-by to say hello and give support to the #LoveDown #Freedom camp on Shepherd's Bush Green, London. #3rdSummerOfLove

Please subscribe to the YouTube and Telegram channel for more videos:
https://youtube.com/user/seanedwardfitz
Telegram: t.me/deliveringliberty

https://d-dean.medium.com/bare-life-and-the-vaccine-giorgio-agamben-775ad3efd79e

Here Agamben explains his concept of "bare life" and adds this at the end:

"Where is the figure of bare life today in question in the handling of the pandemic? It is not so much the sick person, who is isolated and treated as never before in the history of medicine; rather, it is the infected one, or more particularly the asymptomatic unwell [il malato asintomatico], as he has come to be called in a contradictory expression — something that any man is, virtually, and without knowing it. At issue is not so much health, but a life that is neither healthy nor sick, which, as such and as potentially pathogenic, can be deprived of its freedoms and subjected to prohibitions and controls of all kinds. All men are virtually asymptomatic patients in this sense. The only identity of this life, fluctuating between sickness and health, is as the recipient of swabs and vaccines, which, like baptism for a new religion, define the inverted figure of what was once called citizenship. This baptism isn’t indelible, but necessarily provisional and renewable; the new citizen, always required to present his health certification, will no longer have inalienable, inseparable rights [inalienabili e indecidibili], only obligations that must be constantly decided and updated."

PFIZER’s REPORT:

In their trial of just 1,131 children age 12 to 15:

life threatening events 0.1%
diarrhoea 8%
vomiting 3%
headaches 65%
fever 20%
fever > 40°C 0.1%
severe adverse event 0.6%
severe injection-site pain 1.5%
adverse events reported 3%

This means Pfizer predicts causing in EVERY 10,000 CHILDREN:

10 (0.1%) in life-threatening condition
800 (8%) diarrhoea
300 (3 %) vomit
6500 (65 %) headaches
2000 (20 %) fever >40°C
60 (0.6%) severe adverse event
150 severe pain 1.5%
300 (3%) adverse events

Parent to be told?
https://www.nejm.org/doi/10.1056/NEJMoa2107456