Deep sequencing of the Moderna and Pfizer bivalent vaccines identifies contamination of expression vectors designed for plasmid amplification in bacteria
Deep sequencing of the Moderna and Pfizer bivalent vaccines identifies contamination of expression vectors designed for plasmid amplification in bacteria
Deep sequencing of the Moderna and Pfizer bivalent vaccines identifies contamination of expression vectors designed for plasmid amplification in bacteria. February 16th 2023 Introduction As universities in the United States continue to mandate liability-free injections (COVID vaccines) for students at limited risk of contracting COVID, it becomes imperative that more public information be made available for the ingredients of these experimental vaccines. Both the
One of the most important pieces of independent research carried out since the pandemic began. Why it’s being left to independent researcher’s and not the manufacturer’s or regulators to make this information publicly available is an open question for our times. Thank you Kevin for this work, every single person needs to be aware.
Well done. I strongly recommend submission for peer review to timestamp these important results.
I am happy to consider a paper for peer review in Science, Public Health Policy & the Law. The proteins of the replication-competent can also now be considered potential triggers of pathogenic priming by cross-reactive autoreactogenic epitopes. - James Lyons-Weiler
I would be very wary of taking government (Australian) figures seriously. 96% vaccinated is ludicrously exaggerated. Anecdotal but Catherine Austin Fitts makes the same point: the middle class are, and the working class aren't.
err.....isn't this the sort of basic QA stuff that should be done BEFORE starting a Phase I clinical trial??
Shouldn't rigorous analysis of this sort of QA be the primary function of regulators when deciding whether to issue a license to perform early stage clinical trials??
Why is this being done after a billion and more people have been injected with the stuff??
'Let's all expose the world to a nuclear bomb and then learn afterwards what the effects of that sort of radiation exposure has on the human immune system....'
Wow - the more you look the worse it gets! Thanks for doing this important work and for setting an example. It's time for the worlds’ scientists to get back to work as in applying the tools available to inquire into these areas. It IS possible to know much of this - you just have to look and as you've pointed out it doesn't require a lot of money. Tens of thousands (100s?) of labs have everything they need. I have a background in molecular biology (PhD 1995) and I share Jessica's enthusiasm for how cool this stuff is (I contributed to identifying gene mutations responsible for heritable diseases in mice, humans and dogs and it's pretty exciting work). And so I'm familiar with many of the techniques that you've discussed in this post but doing things in the lab is one thing and actually injecting people with foreign genetically manipulated material another. You've brought up some additional questions that need answers and the effects on the microbiome is a big one if this were to become a reservoir for endless spike production as well as the antibiotic resistance potential as bacteria regularly share genetic material. As we get more and more pieces to the puzzle of this horror, I have to mention the link Jessica recently posted to a roundtable with Michael Yeadon called Toxic by Design. So many bad ideas THAT WERE KNOWN combined in these shots (as well as a few unknown – just in case). Oh, the humanity!
So strange that all of the "accidents" like all of the spike-protein mutations seem to "coincidentally" have specific functionalities that are harmful, not just random sludge...
Multiple antibiotic resistance genes! Will wonders never cease?
I'll include this in my next blog post, likely tomorrow.
God help us against this witch’s brew of Lord knows what? To take an injection from these vials is like playing Russian Roulette with a psychopathic demon’s gun. I feel so sorry for the vast number of my family, friends, coworkers and fellow citizens here in Canada who fell for this ‘kill-shot’. It’s heart breaking and it cannot be undone. How many trusting children will suffer for their parents manipulated fear? The local city’s newspaper, radio and television stations broadcast death counts every day in ceaseless propaganda for over a year. 😢 I don’t recognize my country anymore. What is yet to come? I’m beginning to fear the ‘Zombie apocalypse’ hyped for years in the media is a foreshadowing of what is to come as the genetic results of this misbegotten poison jab accumulates to critical mass. Sorry to be such a downer but this article is alarming in its potential scope.
Due to the fact that the Moderna as well as the Pfizer plasmid carry a f1 ori, have you tried to use the vacine, maybe upon opening of the LNPs, for direct transformation of E. coli competent cells?
This would be a more direct proof for intact plasmids that can mediate resistance. In addition you would obtain single plasmids upon replication in E coli cells for resequencing and resolving the problems with the different spike protein variants.
You took quite a risk doing this work, tampering with government property. On behalf of humanity, thank you.
Gonna Substack this Substack. Man oh man.
One of the most important pieces of independent research carried out since the pandemic began. Why it’s being left to independent researcher’s and not the manufacturer’s or regulators to make this information publicly available is an open question for our times. Thank you Kevin for this work, every single person needs to be aware.
Well done. I strongly recommend submission for peer review to timestamp these important results.
I am happy to consider a paper for peer review in Science, Public Health Policy & the Law. The proteins of the replication-competent can also now be considered potential triggers of pathogenic priming by cross-reactive autoreactogenic epitopes. - James Lyons-Weiler
Hi this is great. If it's ok with you I'd like to include some of this in my article.
As a few questions I feel I should know the answer to:
•Have they been able to demonstrate any types of issues exist with introducing the SV40 promoter into humans?
•Did you also sequence the mRNA present (I think you did, but I just want to make sure).
And yet, we are the heroes we are looking for. Welcome to the Thunderdome all.
I would be very wary of taking government (Australian) figures seriously. 96% vaccinated is ludicrously exaggerated. Anecdotal but Catherine Austin Fitts makes the same point: the middle class are, and the working class aren't.
err.....isn't this the sort of basic QA stuff that should be done BEFORE starting a Phase I clinical trial??
Shouldn't rigorous analysis of this sort of QA be the primary function of regulators when deciding whether to issue a license to perform early stage clinical trials??
Why is this being done after a billion and more people have been injected with the stuff??
'Let's all expose the world to a nuclear bomb and then learn afterwards what the effects of that sort of radiation exposure has on the human immune system....'
https://twitter.com/pandata19/status/1633458251403763713?s=46&t=Tsl-3F33wzmMqLy5S3XYVg
Wow - the more you look the worse it gets! Thanks for doing this important work and for setting an example. It's time for the worlds’ scientists to get back to work as in applying the tools available to inquire into these areas. It IS possible to know much of this - you just have to look and as you've pointed out it doesn't require a lot of money. Tens of thousands (100s?) of labs have everything they need. I have a background in molecular biology (PhD 1995) and I share Jessica's enthusiasm for how cool this stuff is (I contributed to identifying gene mutations responsible for heritable diseases in mice, humans and dogs and it's pretty exciting work). And so I'm familiar with many of the techniques that you've discussed in this post but doing things in the lab is one thing and actually injecting people with foreign genetically manipulated material another. You've brought up some additional questions that need answers and the effects on the microbiome is a big one if this were to become a reservoir for endless spike production as well as the antibiotic resistance potential as bacteria regularly share genetic material. As we get more and more pieces to the puzzle of this horror, I have to mention the link Jessica recently posted to a roundtable with Michael Yeadon called Toxic by Design. So many bad ideas THAT WERE KNOWN combined in these shots (as well as a few unknown – just in case). Oh, the humanity!
So strange that all of the "accidents" like all of the spike-protein mutations seem to "coincidentally" have specific functionalities that are harmful, not just random sludge...
Multiple antibiotic resistance genes! Will wonders never cease?
I'll include this in my next blog post, likely tomorrow.
God help us against this witch’s brew of Lord knows what? To take an injection from these vials is like playing Russian Roulette with a psychopathic demon’s gun. I feel so sorry for the vast number of my family, friends, coworkers and fellow citizens here in Canada who fell for this ‘kill-shot’. It’s heart breaking and it cannot be undone. How many trusting children will suffer for their parents manipulated fear? The local city’s newspaper, radio and television stations broadcast death counts every day in ceaseless propaganda for over a year. 😢 I don’t recognize my country anymore. What is yet to come? I’m beginning to fear the ‘Zombie apocalypse’ hyped for years in the media is a foreshadowing of what is to come as the genetic results of this misbegotten poison jab accumulates to critical mass. Sorry to be such a downer but this article is alarming in its potential scope.
Just when I was hoping to have a good night’s sleep!
The jabs were always the intended illness vectors.
The picture below is the REASON for the last 3+ years of insanity.
https://files.catbox.moe/lgumsu.PNG
The banks are BROKE.
We are actually in the 4th year of this madness.
Year 1 - 2020
Year 2 - 2021
Year 3 - 2022
Year 4 - 2023
Thank you for the approach and for sharing.
Due to the fact that the Moderna as well as the Pfizer plasmid carry a f1 ori, have you tried to use the vacine, maybe upon opening of the LNPs, for direct transformation of E. coli competent cells?
This would be a more direct proof for intact plasmids that can mediate resistance. In addition you would obtain single plasmids upon replication in E coli cells for resequencing and resolving the problems with the different spike protein variants.