They are coming for your pets. But they don't tell you it's saRNA tech in their bullshit marketing speel, and they certainly don't want you to see the raw data:
USDA Approves MSD Animal Healthâs NOBIVACÂŽ NXT Canine Flu H3N2 â The First and Only RNA-Particle Technology Vaccine for Canine Influenza
"... NOBIVAC NXT is a revolutionary, first-of-its-kind vaccine technology for companion animals that leverages RNA-particle technology, allowing for a precise immune response to protect against a wide range of viral and bacterial pathogens."
"... NOBIVAC NXT Canine Flu H3N2 is a nonadjuvanted, low volume 0.5 mL dose vaccine that harnesses the natural ability of the immune system to generate a robust response without compromising comfort or safety."
Efficacy and Safety in Dogs Following Administration of an Alphavirus RNA Particle Canine Influenza H3N2 Vaccine (2024)
"... Alphavirus-derived RNA particles (RP), particularly those based on Venezuelan equine encephalitis virus (VEEV), are a compelling platform for the development of vaccines [10,11]. The RP utilizes alphavirus coat proteins to deliver a propagation-defective, self-amplifying RNA to cells in vivo, where the viral replicase drives RNA amplification and efficient protein expression of inserted antigen-coding sequences [12]. "
"... Data Availability Statement
The datasets presented in this article are unavailable because the data are proprietary information of Merck Animal Health."
Why are the pharmacokinetic studies so difficult with these compounds? Fifty years ago when I was a student I could get a 25 ml bottle of D2O in the lab. Even without a radiological licence it should not be that challenging to measure excretion of deuterated LNP's or nucleic acids.
I have not used fluorescent markers as most of the protein chemistry science seems to use, but the whole scheme seems intentionally incompetent.
At a drug dinner a few years ago the corporate scientists had pulmonary distribution slides of the deposition of their inhalation bronchodilators. I can't remember if they were fluorescence or radiation tags, but this is not rocket science.
Thank you for this painstaking and painful review.
Do you think double masks might protect us from the exhaled saRNA's or do we need our full hazmat suits again?
Regarding transfection of saRNA by shedding, two cases i wonder about:
1) the exosome hits skin, which doesnt have the same mucosal defenses;
2) the exosome hits mucosa of previously mRNA injected people (who may not want saRNA jabs for whatever reasons), who have IgG4-based tolerance for spike-like antigens.
The thing is, we don't know if these spike proteins are produced in the endoplasmatic reticulum like BNT162B2 or in the cytosol. As it is a transmembrane protein it should be produced in the ER or it would clump. But we don't know. If it is not produced in the ER it might not shed as much als BNT162B2 but just fill the cells with clumping protein.
Cyprinus Carpio, another masterpiece to the puzzle.
"I am concerned that it could eventually integrate into the RNA of a wild-type alphavirus, leading to gain of function or/and zoonotic transmission"
A Xmas gift... Look to its E1 glycoprotein (Class II viral fusion protein) and what it is "not predicted" to do. What we know - little, what we do not - immense. Enjoy.
You're a bit late. This might already have happened with the adenovirus jabs. They might have crossed with wild type hume adnoviruses years ago. Unfortunately, nobody checked that.
"You're a bit late." Your presumptive. Never late to point out a known fact. If it were, then pointing out something known since 01, is not as "late" as pointing out something else known since 57. "Unfortunately, nobody checked that." More presumption, Those who hide behind omission, are ever "late" and Gibbs Rule 39 & 39A apply.
Reminds me, I wrote about this nearly 3 years ago:
... In other words the coronavirus vaccine ChAdOx1 adenovirus had the gene for E1B protein silenced so that once it has created the spike protein in your cell it is inert or attenuated.
...Except that the viral RNA is quite able to get the machinery back through recombination with other viruses, the part of the first paper as in "and 55K-deleted E1B driven by the cytomegalovirus (CMV) promoter.".
Another name for a CMV? Herpes. And it's everywhere. And the researchers were fully aware of the risks of off-target collateral damage:
Also, viruses assemble spontaneously and also take host genes with them. Any normal Virus can take the modRNA into its capsid by pure chance. That's a normal procedure. The modRNA might also be found in other viruses which coinfected cells.
"viruses assemble spontaneously" Not all, only single stranded with simple structure viz icosahedral, such as picorna and parvo. Viruses with more complex architecture require scaffolding via viral chaperone proteins requiring orchestration, which is anything but spontaneous.
arcturus patents contain literally HUNDREDS of different nucleotides with which the natural messenger RNA can be substituted with. From all the above it is still not clear what it really is in the injection materials. Kevin is right, what's patented can't be natural. In particular when looking at the lifetime of the measured xyzRNA)?) amounts in BLOOD... And placebo is not defined either... Is it saline, if so why does it cause almost IDENTICAL side effects as the real stuff does. That alone is always indication that the 'safety studies' by pharma cartels, stink, a lot.
That on top of everything makes this entire endeavor the next level crime, since one thing was omitted here. What about people carrying other viruses, genetic material from previous injections? Can that stuff all get translated by the replicons and kill even sooner? The sequences listed in their countless patents call for frequent -PP- mutations, exactly like the one added into Spike... WHy? Because it is NOT digestible.
The EU political arena is disgusting, carrying bought out by NOBODY elected individuals, like von der Leyen, who should have been in prison LONG TIME AGO!
They are coming for your pets. But they don't tell you it's saRNA tech in their bullshit marketing speel, and they certainly don't want you to see the raw data:
USDA Approves MSD Animal Healthâs NOBIVACÂŽ NXT Canine Flu H3N2 â The First and Only RNA-Particle Technology Vaccine for Canine Influenza
"... NOBIVAC NXT is a revolutionary, first-of-its-kind vaccine technology for companion animals that leverages RNA-particle technology, allowing for a precise immune response to protect against a wide range of viral and bacterial pathogens."
"... NOBIVAC NXT Canine Flu H3N2 is a nonadjuvanted, low volume 0.5 mL dose vaccine that harnesses the natural ability of the immune system to generate a robust response without compromising comfort or safety."
https://www.msd-animal-health.com/2024/06/25/usda-approval-nobivac-nxt-civ/
***
Efficacy and Safety in Dogs Following Administration of an Alphavirus RNA Particle Canine Influenza H3N2 Vaccine (2024)
"... Alphavirus-derived RNA particles (RP), particularly those based on Venezuelan equine encephalitis virus (VEEV), are a compelling platform for the development of vaccines [10,11]. The RP utilizes alphavirus coat proteins to deliver a propagation-defective, self-amplifying RNA to cells in vivo, where the viral replicase drives RNA amplification and efficient protein expression of inserted antigen-coding sequences [12]. "
"... Data Availability Statement
The datasets presented in this article are unavailable because the data are proprietary information of Merck Animal Health."
https://pmc.ncbi.nlm.nih.gov/articles/PMC11511248/
Why are the pharmacokinetic studies so difficult with these compounds? Fifty years ago when I was a student I could get a 25 ml bottle of D2O in the lab. Even without a radiological licence it should not be that challenging to measure excretion of deuterated LNP's or nucleic acids.
I have not used fluorescent markers as most of the protein chemistry science seems to use, but the whole scheme seems intentionally incompetent.
At a drug dinner a few years ago the corporate scientists had pulmonary distribution slides of the deposition of their inhalation bronchodilators. I can't remember if they were fluorescence or radiation tags, but this is not rocket science.
Thank you for this painstaking and painful review.
Do you think double masks might protect us from the exhaled saRNA's or do we need our full hazmat suits again?
Agreed, - it's not CAN'T, but WON'T, because the information is not helpful for demonstrating product safety.
Instead of external PPE I would work on your own version, that generally works very well, and support it with C D Zinc Mg, diet etc.
Regarding transfection of saRNA by shedding, two cases i wonder about:
1) the exosome hits skin, which doesnt have the same mucosal defenses;
2) the exosome hits mucosa of previously mRNA injected people (who may not want saRNA jabs for whatever reasons), who have IgG4-based tolerance for spike-like antigens.
The thing is, we don't know if these spike proteins are produced in the endoplasmatic reticulum like BNT162B2 or in the cytosol. As it is a transmembrane protein it should be produced in the ER or it would clump. But we don't know. If it is not produced in the ER it might not shed as much als BNT162B2 but just fill the cells with clumping protein.
This would make a difference to HSP autoAb formation too.
The regulator asked, but all we got was a luciferase study.
We don't know how these gene jabs work.
Cyprinus Carpio, another masterpiece to the puzzle.
"I am concerned that it could eventually integrate into the RNA of a wild-type alphavirus, leading to gain of function or/and zoonotic transmission"
A Xmas gift... Look to its E1 glycoprotein (Class II viral fusion protein) and what it is "not predicted" to do. What we know - little, what we do not - immense. Enjoy.
https://www.cell.com/cell/fulltext/S0092-8674(01)00303-8?
Wishing you and yours a Happy, Healthy Holiday Season and a prosperous New Year.
You're a bit late. This might already have happened with the adenovirus jabs. They might have crossed with wild type hume adnoviruses years ago. Unfortunately, nobody checked that.
"You're a bit late." Your presumptive. Never late to point out a known fact. If it were, then pointing out something known since 01, is not as "late" as pointing out something else known since 57. "Unfortunately, nobody checked that." More presumption, Those who hide behind omission, are ever "late" and Gibbs Rule 39 & 39A apply.
Reminds me, I wrote about this nearly 3 years ago:
... In other words the coronavirus vaccine ChAdOx1 adenovirus had the gene for E1B protein silenced so that once it has created the spike protein in your cell it is inert or attenuated.
...Except that the viral RNA is quite able to get the machinery back through recombination with other viruses, the part of the first paper as in "and 55K-deleted E1B driven by the cytomegalovirus (CMV) promoter.".
Another name for a CMV? Herpes. And it's everywhere. And the researchers were fully aware of the risks of off-target collateral damage:
https://doorlesscarp953.substack.com/p/adenovirus-hepatitis-in-children
"And the researchers were fully aware of the risks of off-target collateral damage" Indeed, refer to my other response above.
Also, viruses assemble spontaneously and also take host genes with them. Any normal Virus can take the modRNA into its capsid by pure chance. That's a normal procedure. The modRNA might also be found in other viruses which coinfected cells.
If these hybrids a viable is unknown.
"viruses assemble spontaneously" Not all, only single stranded with simple structure viz icosahedral, such as picorna and parvo. Viruses with more complex architecture require scaffolding via viral chaperone proteins requiring orchestration, which is anything but spontaneous.
Thank you NNB. You have a good break too and a prosperous New Year.
The ol' 'Shoot First, ask Questions Later' routine.
Almost guaranteed to bring on mass extermination... and when it jumps from humans to animals ... of life on Earth.
These things will jump to the untreated 'elite', and thus will bring about the eradication of 'them'.
Life got to where it is without the intervention of 'Big pHarma', so Life does not need, Big pHarma. I see it as just a huge money laundering scheme.
forgot, of course, THANK You for posting this precious info! Will link it to my recent post, hope it is ok;)
arcturus patents contain literally HUNDREDS of different nucleotides with which the natural messenger RNA can be substituted with. From all the above it is still not clear what it really is in the injection materials. Kevin is right, what's patented can't be natural. In particular when looking at the lifetime of the measured xyzRNA)?) amounts in BLOOD... And placebo is not defined either... Is it saline, if so why does it cause almost IDENTICAL side effects as the real stuff does. That alone is always indication that the 'safety studies' by pharma cartels, stink, a lot.
That on top of everything makes this entire endeavor the next level crime, since one thing was omitted here. What about people carrying other viruses, genetic material from previous injections? Can that stuff all get translated by the replicons and kill even sooner? The sequences listed in their countless patents call for frequent -PP- mutations, exactly like the one added into Spike... WHy? Because it is NOT digestible.
The EU political arena is disgusting, carrying bought out by NOBODY elected individuals, like von der Leyen, who should have been in prison LONG TIME AGO!