Surely these products were not intended as therapies? Does it matter if they are impure? Proofs that these products do not meet regulatory guidelines can be strung out for years - until we are all under digital ID/CBDC control in a few months and resistance is useless.
They have no legal standards of manufacturing to meet under EUA. (now switched tracks to BLA licensure) Regulatory control does not exist for EUA products.
despite of the millions of published studies dealing with genetic materials, there is still an issue with measuring its quantities, precisely??? sounds equally complicated as the bitcoin business:
Dear Kevin, you are so right, and so brilliant, and Tom Maniatis would be very proud on you. Because precision exceeds everything I ever read. But didn’t following all your thoughts. We can begin to understand that gene And mRna moratorium is immediately needed after all, so not a single human or any animal or plant should be treated like that as we had been treated now by Moderna and BioNTech. So clearly that one of the greatest DNA sequencing expert and DNA analysis expert on the practical level cannot solve these simple problems caused by this stupid genetic vaccine, the moratorium is the only consequence after all.to solve this problem to clear things up with the vaccines, I have to come back to a method, I developed in 1993, just to investigate tiny amounts of CpG island methylation pattern In very few primary Tumor cell lines. It was kind of a new hybrid of
Maxam and Gilbert sequencing, genomic footprinting of cis acting elements, and I called it hpa II tiny fragment mapping. It was the first southern blood in the world, that could detect fragments smaller than 10 base pairs, and worked up to 500 base pairs with a resolution of single base. it works also with mrna of northern blot and after now 30 years, not a single similar method ever has been described. I did not publish it because I wanted to patent it, but later I forgot it. It’s better to forget a method that everybody needs then to be angry on all those who have been stealing that method and make a lot of money out of it so I forgot it. I remember the Ames test which was used worldwide but did not bring Bruce n Ames a penny nor honours. So I better forgot as I am not part of that criminal mafia in science. But this method used on the vaccine, either without purification or purification we could easily use to be probed with the whole Moderna or BioNTech DNA vector as a southern blot and northern blot hybridisation probe.at that time, I labelled probes with a non-radioactive digoxigenin Antibody alkaline phosphatase chemo Luminescent probe that was very long, and gave a very high signal strength to detect very small amounts of genomic DNA in the whole genome background. We also detected single genes in a mitosis chromosome of single cells, using a light fluorescence microscope. Single dna molecule. While PCR in this case can never solve the problems you have, any more fragment southern or northern blot can solve this easily. As this method was able to clearly bring light into differential methylation pattern of CPG island in any gene prior to bisulfit genomic sequencing was invented, even at a single base pair level of fragments, as small as 20 bases, it should easily solve your problem, also with DNA and RNA hybrid, as it works with the naturalisation, urea sequencing Gels. And you can be sure that you don’t find this method or a similar method in the Maniatis or any other protocol collection of the old times. This method will be also useful to detect the integration of plasmid fragments into the whole human genome in a small amount of cells isolated from the blood. Because this is the next step. But better let’s discuss this on protonmail. Thanks for your great research. Arminius
Sneaky 🤡
Amazing how they can purify chemical toxins. Can I stop laughing at these fools?
Surely these products were not intended as therapies? Does it matter if they are impure? Proofs that these products do not meet regulatory guidelines can be strung out for years - until we are all under digital ID/CBDC control in a few months and resistance is useless.
They have no legal standards of manufacturing to meet under EUA. (now switched tracks to BLA licensure) Regulatory control does not exist for EUA products.
https://sashalatypova.substack.com/p/mainstream-media-coverage-of-the
Achs is on a lower level of intellect, clearly.
That said, you should be on Joe Rogan.
despite of the millions of published studies dealing with genetic materials, there is still an issue with measuring its quantities, precisely??? sounds equally complicated as the bitcoin business:
https://www.youtube.com/watch?v=blXvZ0I8GdI
Dear Kevin, you are so right, and so brilliant, and Tom Maniatis would be very proud on you. Because precision exceeds everything I ever read. But didn’t following all your thoughts. We can begin to understand that gene And mRna moratorium is immediately needed after all, so not a single human or any animal or plant should be treated like that as we had been treated now by Moderna and BioNTech. So clearly that one of the greatest DNA sequencing expert and DNA analysis expert on the practical level cannot solve these simple problems caused by this stupid genetic vaccine, the moratorium is the only consequence after all.to solve this problem to clear things up with the vaccines, I have to come back to a method, I developed in 1993, just to investigate tiny amounts of CpG island methylation pattern In very few primary Tumor cell lines. It was kind of a new hybrid of
Maxam and Gilbert sequencing, genomic footprinting of cis acting elements, and I called it hpa II tiny fragment mapping. It was the first southern blood in the world, that could detect fragments smaller than 10 base pairs, and worked up to 500 base pairs with a resolution of single base. it works also with mrna of northern blot and after now 30 years, not a single similar method ever has been described. I did not publish it because I wanted to patent it, but later I forgot it. It’s better to forget a method that everybody needs then to be angry on all those who have been stealing that method and make a lot of money out of it so I forgot it. I remember the Ames test which was used worldwide but did not bring Bruce n Ames a penny nor honours. So I better forgot as I am not part of that criminal mafia in science. But this method used on the vaccine, either without purification or purification we could easily use to be probed with the whole Moderna or BioNTech DNA vector as a southern blot and northern blot hybridisation probe.at that time, I labelled probes with a non-radioactive digoxigenin Antibody alkaline phosphatase chemo Luminescent probe that was very long, and gave a very high signal strength to detect very small amounts of genomic DNA in the whole genome background. We also detected single genes in a mitosis chromosome of single cells, using a light fluorescence microscope. Single dna molecule. While PCR in this case can never solve the problems you have, any more fragment southern or northern blot can solve this easily. As this method was able to clearly bring light into differential methylation pattern of CPG island in any gene prior to bisulfit genomic sequencing was invented, even at a single base pair level of fragments, as small as 20 bases, it should easily solve your problem, also with DNA and RNA hybrid, as it works with the naturalisation, urea sequencing Gels. And you can be sure that you don’t find this method or a similar method in the Maniatis or any other protocol collection of the old times. This method will be also useful to detect the integration of plasmid fragments into the whole human genome in a small amount of cells isolated from the blood. Because this is the next step. But better let’s discuss this on protonmail. Thanks for your great research. Arminius
Check out Free Nz SubStack with an interview with the Canadian scientist David Speicher.
https://freenz.substack.com/p/dr-david-speicher-dna-contamination
They have an excellent short video called DNA in mRNA vaccines - which explains why there are DNA in the vaccines in the first place. I liked it.
Thank you.