The Liberty Beacon
In a recent publication by a group of experienced geneticists, more contamination in mRNA “vaccines” (Pfizer and Moderna), excluding metal residues, which had been identified in the past, was found. Multiple methods highlighted high levels of DNA contamination.
Of special concern was that they found replicable DNA, so-called plasmids, in both the monovalent and bivalent vaccines, which should not be there at all. This time the researchers found DNA contamination that far exceeded the European Medicines Agency (EMA) requirement and the U.S. FDA’s dose requirements.
But why is this find so alarming?
Karen Kingston also digs down into this below. The problem is, as she says, it’s NOT ‘CONTAMINATION’. The replicable DNA or ‘plasmids’ are a PFIZER INGREDIENT. Designed to do what? Change our DNA by introducing NEW components. And we don’t even know this is happening.
Plasmid DNA is a Known Pfizer Ingredient – NOT a Contaminant
On June 7, 2021, AGC Biologics announced that they were the supplier of plasmid DNA for the manufacturing of the BioNTech/Pfizer mRNA ‘vaccines’
Recent experts have come forward confirming that plasmid DNA is in Pfizer’s mRNA vials and that plasmid DNA is for purposes of the expression on non-human DNA inside humans through cell transfection.
I first reported on the existence of plasmid DNA as an ingredient in the Pfizer’s mRNA vials on October 20, 2021 on Brannon Howse. I begin my presentation on plasmid DNA at around the 32:25.
Transcript of Karen Kingston October 20, 2021 Report on Plasmid DNA in Pfizer mRNA ‘Vaccines’
“We were never told what was in these vials and that is criminal. And I just want to be clear that this does change your DNA.”
This is a press release that was put out on June 7, 2021. AGC Biologics is one of the top manufacturers of biological agents and gene therapies, etc. in the industry.
This is a quote from their former Chief Business Officer. Mark has gone onto another organization. I’ll just read the press release.
“We are honored that BioNTech has entrusted us to become part of their global supply network in an effort to make the vaccine available to as many people as possible around the world,” says AGC Biologics Chief Business Officer, Mark Womack. “We are very proud of our efforts to provide our global customers with the essential materials needed to rapidly deliver vaccines in the fight against the COVID-19 pandemic.”
AGC Biologics will manufacture and supply BioNTech with the plasmid DNA starting material, an essential component of BioNTech’s mRNA-based vaccine manufacturing process.
Why is that alarming? Because nobody was told that they were injected with plasmid DNA!
“We were never told what was in these vials and that is criminal. And I just want to be clear that this does change your DNA. Why is that alarming? Because nobody was told that they were injected with plasmid DNA.” – Karen Kingston, October 20, 2021
What is Plasmid DNA?
Plasmid DNA is used for a number of applications including transfection – which is the insertion of genetic materials into your cells. Sequencing. Clones – we know what clones are – they’re clones. Restriction digestion – which is when you cut and paste DNA into different parts of a genetic sequence. And PCR is the polymerase chain reaction- so that is the mapping out a full DNA code and then taking what’s called a codon and copy pasting, copy pasting.
The main point of plasmid DNA is to help with integration of new genetic material into a (human) being. Just… that’s what it is.
Brannon: Say that last sentence again.
So the purpose of the plasmid DNA is to help with the integration of genetic material into a (human) being.
Brannon: And the question would be, “What genetic material?” Right?
Yeah. It (pDNA) can integrate viral genetic material. It can integrate genetic material from other species. It can integrate bacterial genetic material.
I mean, no one was told about this, and if you’re going to say to me ‘This doesn’t prove (the vials) contain plasmid DNA,’ then write the board of AGC Biologics and tell them that they’re lying Reuters.
Brannon: Is this the first time you presented this?
Yeah. You called me to talk about luciferase, so I put this together for you.
So I told you what transfection means, Thermo Fisher, this is their definition, “it’s the process of artificially introducing DNA and RNA into cells. It can result in changes to to the properties of the cell.”
This is a Genetic Change to Your Genetic Make-Up
This is a genetic change to your genetic make-up.
“And Reuters! Go pound sand! If you say what I’m saying is false, send a letter to Thermo Fisher Scientific. Tell them to take down this definition.”
Brannon: Can result in the changes of the properties of the cell. So now these guys are injecting stuff into people to change the very make-up of their cell and their DNA?
Yes. So one of the make-up of the cells is you could have perfectly healthy cells that will now not go through natural cell death and have HeLa injected into them, so now you’ve got an aggressive cancerous cells that are forming tumors in your body. So that’s one change.
There could also be interspecies changes, but we don’t have time to go through that today. (end of transcript)
Is Pfizer Liable for Genetic Damage and Harm Caused by Plasmid DNA in their mRNA Vials?
Yes. Because due to Pfizer’s contract with the US Army, Pfizer is legally bound to the US laws regulating good manufacturing practices (GMP) for their FDA-approved mRNA ‘vaccines’ and good lab practices (GLP) for human clinical trials and emergency use authorized mRNA ‘vaccines’. This means that all of the substances in Pfizer’s mRNA vials have to be proven to be safe for human use. If any of the ingredients are not safe, Pfizer is liable for the injuries and deaths caused by any chemicals, toxins, or other harmful substances contained in their mRNA vials.
Under the Manufacturing Development Plan of Pfizer’s contract, it specifically states, “…the manufacturing process for the vaccine product to ensure conformity with 501(a)(2)(B) of the Food, Drug and Cosmetics Act (FD&C Act, Title 21 United States Code (USC) regarding good manufacturing practices (GMP).”
Per section 501(a)(2)(B) of the FD&C Act, a drug (or biologic) Pfizer must ensure that they follow good manufacturing practices to ensure that their mRNA injections meet the requirements of safety of any FDA-approved or authorized product for human use.
This means all substances in the vials must be safe for human use. The contract states that, “Pfizer shall scale up its capabilities for….manufacture, analysis, and release of GMP materials (mRNA).”
Analysis means that Pfizer will ensure quality control testing of the final product’s purity and consistency at the manufacturing facilities.
Many experts have proven that there are toxic levels of plasmid DNA, graphene oxide, and other substances harmful to humans found in the mRNA vials, as well as finding no mRNA itself in the vials. These findings are clear violations of Pfizer’s DOD contract and the laws that govern EUA and FDA-approved products.
Claiming Pfizer is Not Subject to FDA Manufacturing or Safety Laws is Extrinsic Fraud
An alleged expert in contracting large clinical trials for pharmaceutical and medical device companies has claimed that all mRNA injections are Emergency Use Authorized (EUA) countermeasures and that they can not constitute a clinical investigation or comply with current Good Manufacturing Practices and US regulatory laws.
These are false and reckless statements from a revered clinical trial contract expert. If used in a court of law, this type of ‘expert’ testimony could quite literally enable Pfizer to get away with murder.
The Kingston Report. TRUTH WINS.
To this day, I am perplexed as to why experts and attorneys do not believe the facts and evidence I presented in 2021 and continue to present today. May God help us.