I see this as a major upgrade. I wonder if it would be sensitive enough to detect the vaccine contaminants in the blood of recently-vaccinated patients (although many of them would probably rather not know).
If it is sensitive enough, you might be able to correlate subsequent contaminant-related AEs with the type and batch# of the vaccine used if you could get enough blood specimens.
The problem we have here in the deep state of Australia is no one wants to touch this with a ten foot pole. We are struggling to get a long covid clinic let alone a vaccine injury clinic. These tests should be running across our country not only for “those worried” but for those INJURED! In fact they should be locked into a nation wide testing protocol! Thanks for all you amazing work! Keep it up!
This is very important: the facts coming out showing the vaxx-protocols were “intentionally not made exactly the same.” It’s important to “understand” these bioweapons have varied ingredients—lab by lab, batch by batch, region by region, with a well-panned timeline of varied stages to be unleashed on the general public—which have varied differences and purpose. This includes the evolution of the common-cold-causing coronavirus harvested from nature that have been modified into what’s known as COVID-19 (starting prior to 2015 in the United States, Texas, then shipped to China, Ukraine…)
It’s important for all the researchers, worldwide, to start communicating and bringing all this data together, in full sunlight, so all the researchers, including the general public, “understand” that the ingredients of each vaxx within “some of the batches” were varied, including some batches containing empty banks (not placebos as most doctors & researchers use for legitimate scientific research & “understanding” of effectiveness).
This is a well planned bioweapons program with multiple purposes “they” still expect to deliver over many years, with the help of their very controlled media, politicians, directors of investigative agencies, judges, attorney generals, and many million high ranking police throughout the entire world. This Crime Against Humanity has been developing for centuries, not just the past three years. As AI science has evolved over the past few decades, they have been methodically building on their “understanding” of mRNA & microdot science being developed as well—not only for their mass genocide program—but also for organ harvesting, DNA manipulation and eventually complete control over the remaining sheeple, until they no longer need the less-than-human lab-rats they allowed to remain, and will kill them, too. Diabolical doesn’t even come close to describing what’s really going on, and right in plain sight.
This is not a conspiracy theory, but an ongoing, real conspiracy against humanity by just a slim few (less than one-tenth of one percent—of the one percent—at the very top of this very sick pyramid); Criminally-Insane, Eugenicist, money-junky, ultra-wealthy Trillionares—who control their complicit ultra-rich few billionaires—who control their rich, inhuman tool-assets of government and media talking-heads, who have done an exceptional job keeping their brainwashed, warring constituent-sheep (us, the people majority) psychologically-divergent to accept this madness for several generations.
We must wake up, now, peacefully resist, arrest these few monsters and stop pretending we can’t. If We the People majority do not stop believing in the more expensive, bloody wars against each-other and start believing in eliminating and liquidating just the very few ultra-rich monsters—humanity is dead.
Is SV40 in the ModeRNA vaxx version as well? When you comment on the bottom that monocytes have the most persistent spike are you referring to the vaxx spike or the actual covid spike? Does the spike from the actual infection persist and replicate just like the vaxx? These are important questions for all of us I think. I’m not vaxxed but did have 2 bouts of what was probably covid; I wouldn’t test either- God knows what was on those swabs!!
In the substack you are commenting on, Kevin said near the top: "To do this, we targeted the 72bp tandem repeat (also known as the bidirectional Enhancer element) in the Pfizer vaccine. This assay will not work on the Moderna vaccines as they do not contain this sequence."
In terms of the RAT, you didn't need to use their swabs. An ordinary cotton bud was just as efficient.
Nuclear localization is likely very relevant for hematopoietic stem cells if transfection is reaching the marrow. They are very dependent on V(D)J recombination I believe. I hope these shots don't go that far, but the Moderna slides claiming mouse marrow transfection with similar LNPs and PEG have me worried. Monocytes should absolutely be first though, they are on identification and cleanup duty.
Also: it may be possible to use something like this to vindicate work like Arne's, right? He checked internal lesions for S1 subunit, but that was denied due to N protein not reproducing in all tissues. If the cells can be biopsied from the lesions (or local monocytes that have eaten away the tissue collected) and shown to have dsDNA contaminants however, it would be pretty strong vindication/verification for work like his IMO
Possibly an impossible question.... How much has the spike of the latest sars-cov2 'variant', mutated and differed from the two spikes in the bivalent Pfizer?
The proteins are all split into identifiable sections, and the full viral nucleotide genome is on the bottom. That being said, I'm betting the Omicron half is not that far off most current circulating versions. However Omicron has something like 6 indels and 30 mutations in the spike protein compared to Wuhan Hu 1 (spike is most mutated protein I think). The Wuhan Hu1 portion is now incredibly ecologically irrelevant, and I can't find a single scientific reason why it's still there, provided my assumption is right and they are still using the original spike from the original monovalent
In a unicorn world, starting small, how/from where would you like to get blood samples? In what form? How many? With what information (anonymized to you, of course)
Any sequencers near Cleveland? In your State? Who could rustle up samples? How much cash would that take for time, materials, cycles on the machinery?
NRN, just brainstorming. Spouse ran UNF’s sponsored research program, FWIW, in one of his many previous job lives. CFO for three Navy regions in others.
Sounded like someone replicated with more vaccine samples—yay!
My dad was injured by the vaccine and got two of the worst lots according to how bad is my batch. He continues to have issues to this day. Do you know a doctor willing to do this assay? Thanks
Thank you Kevin. The truth will prevail. We are fortunate that you are doing this work. Peace.
I see this as a major upgrade. I wonder if it would be sensitive enough to detect the vaccine contaminants in the blood of recently-vaccinated patients (although many of them would probably rather not know).
If it is sensitive enough, you might be able to correlate subsequent contaminant-related AEs with the type and batch# of the vaccine used if you could get enough blood specimens.
I agree with your premise. It certainly would help a lot of people who are worried, rightly so, about what was injected into them. Peace.
The problem we have here in the deep state of Australia is no one wants to touch this with a ten foot pole. We are struggling to get a long covid clinic let alone a vaccine injury clinic. These tests should be running across our country not only for “those worried” but for those INJURED! In fact they should be locked into a nation wide testing protocol! Thanks for all you amazing work! Keep it up!
A lawsuit filed on 6/7/23
🛑 Federal Court of Australia
Doctor Julian Fidge
Applicant
Pfizer Australia Pty Ltd
First Respondent
Moderna Australia Pty Ltd
Second Respondent
“The matter concerns an application for an injunction pursuant to section 147 of the Gene Technology..”
https://twitter.com/myletrinh123/status/1678595149717463042?s=20
More information here if your interested in the lawsuit:
https://andrewmadry.substack.com/p/new-legal-proceedings-in-australia
This is very important: the facts coming out showing the vaxx-protocols were “intentionally not made exactly the same.” It’s important to “understand” these bioweapons have varied ingredients—lab by lab, batch by batch, region by region, with a well-panned timeline of varied stages to be unleashed on the general public—which have varied differences and purpose. This includes the evolution of the common-cold-causing coronavirus harvested from nature that have been modified into what’s known as COVID-19 (starting prior to 2015 in the United States, Texas, then shipped to China, Ukraine…)
It’s important for all the researchers, worldwide, to start communicating and bringing all this data together, in full sunlight, so all the researchers, including the general public, “understand” that the ingredients of each vaxx within “some of the batches” were varied, including some batches containing empty banks (not placebos as most doctors & researchers use for legitimate scientific research & “understanding” of effectiveness).
This is a well planned bioweapons program with multiple purposes “they” still expect to deliver over many years, with the help of their very controlled media, politicians, directors of investigative agencies, judges, attorney generals, and many million high ranking police throughout the entire world. This Crime Against Humanity has been developing for centuries, not just the past three years. As AI science has evolved over the past few decades, they have been methodically building on their “understanding” of mRNA & microdot science being developed as well—not only for their mass genocide program—but also for organ harvesting, DNA manipulation and eventually complete control over the remaining sheeple, until they no longer need the less-than-human lab-rats they allowed to remain, and will kill them, too. Diabolical doesn’t even come close to describing what’s really going on, and right in plain sight.
This is not a conspiracy theory, but an ongoing, real conspiracy against humanity by just a slim few (less than one-tenth of one percent—of the one percent—at the very top of this very sick pyramid); Criminally-Insane, Eugenicist, money-junky, ultra-wealthy Trillionares—who control their complicit ultra-rich few billionaires—who control their rich, inhuman tool-assets of government and media talking-heads, who have done an exceptional job keeping their brainwashed, warring constituent-sheep (us, the people majority) psychologically-divergent to accept this madness for several generations.
We must wake up, now, peacefully resist, arrest these few monsters and stop pretending we can’t. If We the People majority do not stop believing in the more expensive, bloody wars against each-other and start believing in eliminating and liquidating just the very few ultra-rich monsters—humanity is dead.
Is SV40 in the ModeRNA vaxx version as well? When you comment on the bottom that monocytes have the most persistent spike are you referring to the vaxx spike or the actual covid spike? Does the spike from the actual infection persist and replicate just like the vaxx? These are important questions for all of us I think. I’m not vaxxed but did have 2 bouts of what was probably covid; I wouldn’t test either- God knows what was on those swabs!!
In the substack you are commenting on, Kevin said near the top: "To do this, we targeted the 72bp tandem repeat (also known as the bidirectional Enhancer element) in the Pfizer vaccine. This assay will not work on the Moderna vaccines as they do not contain this sequence."
In terms of the RAT, you didn't need to use their swabs. An ordinary cotton bud was just as efficient.
Kevin you say, "This assay may be helpful to track which tissues may have SV40 elements from the Pfizer vaccine still present."
So how would you test for this? If the SV40 is integrated in cellular tissues, what would you test? A blood sample?
I would start with monocytes as those have the most spike persistence.
Others want to look at sperm/stem cells.
Nuclear localization is likely very relevant for hematopoietic stem cells if transfection is reaching the marrow. They are very dependent on V(D)J recombination I believe. I hope these shots don't go that far, but the Moderna slides claiming mouse marrow transfection with similar LNPs and PEG have me worried. Monocytes should absolutely be first though, they are on identification and cleanup duty.
Also: it may be possible to use something like this to vindicate work like Arne's, right? He checked internal lesions for S1 subunit, but that was denied due to N protein not reproducing in all tissues. If the cells can be biopsied from the lesions (or local monocytes that have eaten away the tissue collected) and shown to have dsDNA contaminants however, it would be pretty strong vindication/verification for work like his IMO
Yes.
The DNA sequence for the Vax is very specific to the Vax and shouldn’t cross talk with SARs-CoV2.
There are only 2 prolines that separate the Vax spike from the C19 spike and most protein based assays can’t split them.
Thus they rely on Nucleocapsid which doesn’t show up in some tissues
Possibly an impossible question.... How much has the spike of the latest sars-cov2 'variant', mutated and differed from the two spikes in the bivalent Pfizer?
You need a specific genome to answer that. Any new genome you find, you can compare with the original (Wuhan Hu 1)
https://www.genome.jp/dbget-bin/www_bget?refseq:NC_045512
The proteins are all split into identifiable sections, and the full viral nucleotide genome is on the bottom. That being said, I'm betting the Omicron half is not that far off most current circulating versions. However Omicron has something like 6 indels and 30 mutations in the spike protein compared to Wuhan Hu 1 (spike is most mutated protein I think). The Wuhan Hu1 portion is now incredibly ecologically irrelevant, and I can't find a single scientific reason why it's still there, provided my assumption is right and they are still using the original spike from the original monovalent
Is it true, that Omicron spike has no sequences which resemble prions?
I only wish you'd said "I WILL start with monocytes..."
I really hope this experiment gets done. By many , hopefully.
I don’t have access to clinical samples.
In a unicorn world, starting small, how/from where would you like to get blood samples? In what form? How many? With what information (anonymized to you, of course)
Any sequencers near Cleveland? In your State? Who could rustle up samples? How much cash would that take for time, materials, cycles on the machinery?
NRN, just brainstorming. Spouse ran UNF’s sponsored research program, FWIW, in one of his many previous job lives. CFO for three Navy regions in others.
Sounded like someone replicated with more vaccine samples—yay!
Believe in serendipity.
Thank you.
What about my vaxxed relatives volunteering to provide their samples for you?
The SnapGene diagram show SV40 promoter, but I thought the 72bp repeats were of the SV40 enhancer.
Is that not correct?
My dad was injured by the vaccine and got two of the worst lots according to how bad is my batch. He continues to have issues to this day. Do you know a doctor willing to do this assay? Thanks
Can you make an anti-N with a DNA sub-assembly that you can run qPCR on?
Kevin answered the basic question question here,:
https://anandamide.substack.com/p/lab-visit-and-vsrf/comment/18334761
100%. Dr. Colleen Huber is doing good things reference cancer in AZ.
https://colleenhuber.substack.com/
Also, FYI:
https://fenbendazole.substack.com/
Peace.