I think they were deliberately created as a biological weapon, to depopulate the planet of specific groups,the old, the sick, (physically and mentally) and also ethnically targeted.
I, being 71 at the time of my booster was almost finished off.The maim and kill doses were spread about, easy to kill the old because we are thought to be near death anyway…..
Our Gov’s can’t afford the pensions and we don’t fit into the WEF New World Order ,unless of course you are Fauchi or Klause Schwab!!
Those of us who have survived will die much earlier, but they have overplayed their hand and people are waking up. Too many sportspersons dropping dead, now little children with liver autoimmune desease and all the rest.The evidence is too much to hide.Vaccine hesitancy is higher than ever before and new Medical,Legal and Scientific Frameworks are being set up.I hope it isn’t too late 😊 Thank you Andreas for your astute analysis.
Previously, the Social Security trust fund was projected to start depleting in 2034 and the Medicare Part A trust fund was set to start getting cut in 2026. However, a new annual trustees report showed that the two programs will be able to provide full benefits now until 2035 and 2028 respectively. Just sayin....
Maybe we should take back the billions provided to Pfizer, Moderna etc., all the CovidCon money, ESSER l, ll, lll, etc., as well as Ukraine and the war machine. That might help Social Security just a bit.....just saying!
Great article Andreas. They could have used different protein targets to effective, but they chose the full toxic S spike, with N-terminal domain. Taking in mind, Bill Gates' equation of CO2= PxSxExC. Then suggesting a 10-15% reduction of P with sloppy "vaccines". The FDA's EUA is basically a continuous license to experiment on the human population. And without a method of safely injecting mRNA ( such as, Aspiration before injection), it is known a certain % would enter the blood stream, thus particles traveling to any organ, tissue, brain barrier, would occur. These monsters behind the glass mirror know what is happening, and know every bit of what they did, but don't say anything. That's the crime right there.
of course! from what I could understand, DTRA/DARPA had a scaffolding plan in a phased approach. essentially rapid prototyping of a "vaccine" with the spike pathogen depending on the level of threat. I think this follows with the Monkeypox spike. Plug N Play sort of modules that get integrated into the booster.
Since the "pandemic" started in 2020, I've gotten sick once. Lasted all of three days. Someone close to me on the other hand, who got the shot, has gotten sick more times than I can recall, and usually remains sick for a longer period of time.
Jun 3, 2022·edited Jun 3, 2022Liked by Andreas Oehler
I appreciate your work, thank you.
I'd like to draw your attention to Eleni Papadopulos-Eleopulos' and her Perth group's work on HIV http://www.theperthgroup.com/
Sadly, Eleni passed away not long ago, this year :(
You can find a lot of her presentations, interviews etc., on line. She did an immense service to humanity that has never been recognised. And, she's not alone in what she says.
(Kennedy mentions them briefly in his new book, the Real Antony Fauxi).
It's worth your time to research it further, I believe.
In March 2020, there was a YouTube video posted from a group led by a curious onlooker, someone outside of the accepted science of the international fear mongers group, that debunked the entire NIH story. They stated that what was being visually presented to us as a virus was in fact an exosome, and that there were numerous possible causes for expressing exosomes. Fear being one of them. The video was removed. I can understand why, because they were correct, and Sir Francis Collins, often pictured holding an exosome model from the liver of a monkey, was lying to all of us idiots who would never question his NIH.
It's interesting... Exosomes look exactly like viruses. Spikes on the outside, membrane and then RNA inside. Exosomes seem to be created by cells when they are trying to take out the trash. Viruses are a seperate microbe which has evolved to be highly specialised in the way it infects and interacts with complex organisms despite not being alive or sentient in any way.
Exosomes are poorly understood, but the incredibly complex world of viruses is apparently well understood. It seems like there may be significant overlap between these two domains.
I've already been tramautized enough by Walter Chestnut's theories, I don't need even more in depth information. I keep waiting for my friends and family to turn into giant balls of spike induced fibrin
Yes, weird outlandish projections at the time. One most odd was projecting Russia‘s population to grow. I guess he didn’t see this war coming. The heart of a son of man plans his ways and LORD orders his steps?
Thanks, very informative! What is this talkshow? Btw, they quote about 30 trillion spikes to be produced by the jabbed, from the general math. So we are about right with what I quoted here, as not every mRNA injected will successfully transfect, and some will transfect in bunches the same cell, reducing the throughput.
"Anthony Fauci, Albert Bourla, Stephane Bancel, alongside many others, charged with charged with Genocide in legal filing with the International Criminal Court (ICC)"
What's the big deal! Ukraine gave up so many nukes back in the nineties, in return for the security guarantees from Russia, UK and US, that having 30 or 40kg left over is pocket lint de la pocket lint, comparatively speaking.
I've worked with exosomes for years (they are great for various regenerative medicine applications including restoring internal organs). Since COVID started, we've found exosome therapy is one of the most effective treatments for COVID (acute, long hauler or vaccine injuries) but the exact reason for this has been a bit of a ? for me, and one of the articles you linked to was helpful for filling in some gaps in my understanding. When people put the work to put something together that helps me I like to acknowledge it. Thank you again!
You get them from a good source (they need to come from a mother who was properly screened, I don't find the ones from adult donors work as well) and then inject them intravenously. There are some tricks to getting a better outcome with the injection, but that's beyond the scope of what I could put into writing here. In a few cases, I have seen people have a large improvement in a matter of minutes which still astounds me to witness.
They seem to help a variety of autoimmune conditions (which arguably characterizes long haul covid). I also believe to some extent they turn off the cell danger response:
We all know about myocarditis now, but I recently read an explanation for why it is happening that made perfect sense to me. I was surprised I hadn't read this earlier. I can't guarantee that it is true, but it sure makes sense to me. It also explains why athletes seem to go down so often these days.
The pale-yellow fluid of the Pfizer or Moderna vial contains billions of microscopic fat globs called lipid nanoparticles. Each is an incredibly tiny envelope, used to conceal the novel drug: messenger RNA. Once injected, the combination of nanoparticles and mRNA becomes a well-camouflaged predator.
According to Pfizer’s own data, less than half the nanoparticles stay in the arm where they were injected. Most slip through tiny cracks in muscle tissue and enter the bloodstream. Venous blood speeds them to the heart, which pumps and disperses them to the entire body.
Depending on the level of exercise, from 5 to 25% of these particles wind up in coronary circulation. Why is this important? Consider the rather large number of nanoparticles that must slip into human heart tissue: 50 to 250 million out of each billion that enter the veins of the arm.
Coronary circulation branches into microscopic capillaries that rush nutrients to heart muscle cells. And since the nanoparticles designed by Pfizer and Moderna masquerade as triglycerides, heart muscle cells are apt to snatch them out of circulation as food.
Now imagine the shock for any hard-charging heart cell that engulfs one of these particles. Expecting a meal, the cell unwraps the envelope, and voilà! Freshly unveiled messenger RNA seizes the cell’s protein-generating apparatus, forcing out a known toxin -- the COVID spike protein.
Very soon, with urgent biochemical signals, the afflicted cell telegraphs news of its hijacking to the immune system, which will marshal what it takes to destroy the cell.
An immune-mediated attack on heart muscle cells is, of course, the very essence of myocarditis. Foreign RNA takes control of a cell’s protein production, transforming these cells into enemies of the body, and the immune system converts them into useless scar tissue. The process is irreversible, as heart muscle cells do not regenerate.
I especially like this -- "Now imagine the shock for any hard-charging heart cell that engulfs one of these particles. Expecting a meal, the cell unwraps the envelope, and voilà! Freshly unveiled messenger RNA seizes the cell’s protein-generating apparatus, forcing out a known toxin -- the COVID spike protein."
The only important distinction between the Covid disease and the "vaccination" is that in addition to the S spike code the jab contains about 35-70% of truncated code that may produce truncated, or cut, chunks, of the S spike, so not need to even cut it with the enzymes. Another one is that the translation of mRNA to S spike is also prone to errors and interruptions due to the modifications to the mRNA introduced to increase the spike output. And third, as you have mentioned, much larger number of S spikes all over the organs and tissues, including the brain.
May I ask how do you estimate the number of spike proteins being generated? I have done the estimation myself some time ago but did not write it down and now don't remember what inputs I have used.
Found this calculation of the number of mRNA in Pfizer (30mcg) and Moderna (100mcg):
Calcul du nombre de molécules d'ARNm dans une dose de vaccin
1. Nous obtenons la séquence nucléotidique précise des ARNm à partir du
site de partage de données académiques github.com: Assemblics-of-putative-SARS-CoV2-spike-encoding-mRNA-sequences-for-vaccincs-BNT-162b2-and-mRN A-1273
2. Nous calculons la masse molaire de chacun des ARNs (voir annexe): BioNTech/Pfizer_BNT-162b2_vaccine: 1341,379 kDa (1.341.379 Da)
3. Nous calculons à combien de molécules réelles correspondent les
dosages indiqués (30 microgrammes et 100 microgrammes)
Pfizer : 6.02 10^23 (nombre d'Avogadro) molécules correspondent à 1,341,379 g
30 microgrammes correspondent donc à (6.02 10^23/1,341,379)x 30 x 10^-6 = 1.35 x 10^13
Moderna : 6.02 10^23 (nombre d'Avogadro) molécules correspondent à 1,341,379 g; 100 microgrammes correspondent donc à (6.02 10^23/1,288,795)x 100 x 10^-6 = 4.67 x 10^13
4. Comparaison avec le nombre de virus dans le cas d'infection naturelle: Les nombres ci-dessus sont véritablement astronomiques, quand on sait qu'un
patient est considéré comme très positif avec une valeur de PCR Ct=24, et que
cela correspond à 2.106 virus/ml
L’injection d’une dose de Pfizer délivre donc autant de mRNA de la protéine Spike que ce qui est contenu dans 1.35 × 10^13/( 2 × 10^6) = 0.675 × 10^7𝑚𝑙 de fluide nasal infecté, soit 6750 litres!
Which is 13.5 trillion mRNAs in one Pfizer dose and 46.7 trillion mRNAs in one Moderna dose. Even in just 10% of that is intact, then it's still a trillion or more mRNA molecules per shot.
As to the number of copies, it may be as high as 10,000 per mRNA (https://pubmed.ncbi.nlm.nih.gov/24688849/): ""For [researchers'] corrected data, the median number of proteins translated per mRNA is 9,800 compared to Schwanhausser et al.'s (2011) original estimate of 900 and their second estimate of 2,800. In yeast, the ratio of protein molecules translated per mRNA is 4,200-5,600 (Ghaemmaghami et al., 2003 Lu et al., 2007 BNID 104745, 104185). Given that mammalian cells have a higher protein copy number than yeast (Milo et al., 2010), it is not unreasonable that the ratio in mammalian cells would be higher.""
An average human protein length is being estimated at 400aa. As the S spike in the jab is 1273-1300aa, this is 3X longer. So, from the estimate of 1000-10,000 copies, we can reduce this, at a minimum, to 300 copies of S spikes per mRNA.
This does not take into account that the mRNA in the jab has been translation optimized and pseudouridine-stabilized. So, we have to multiply back 5X-10X. Then, the minimum estimate rises again to 1,500 copies.
So, very conservatively then, 1,000 copies per mRNA - an order of magnitude more than 100 copies per mRNA!
I think they were deliberately created as a biological weapon, to depopulate the planet of specific groups,the old, the sick, (physically and mentally) and also ethnically targeted.
I, being 71 at the time of my booster was almost finished off.The maim and kill doses were spread about, easy to kill the old because we are thought to be near death anyway…..
Our Gov’s can’t afford the pensions and we don’t fit into the WEF New World Order ,unless of course you are Fauchi or Klause Schwab!!
Those of us who have survived will die much earlier, but they have overplayed their hand and people are waking up. Too many sportspersons dropping dead, now little children with liver autoimmune desease and all the rest.The evidence is too much to hide.Vaccine hesitancy is higher than ever before and new Medical,Legal and Scientific Frameworks are being set up.I hope it isn’t too late 😊 Thank you Andreas for your astute analysis.
Previously, the Social Security trust fund was projected to start depleting in 2034 and the Medicare Part A trust fund was set to start getting cut in 2026. However, a new annual trustees report showed that the two programs will be able to provide full benefits now until 2035 and 2028 respectively. Just sayin....
More good news to come shortly!
Maybe we should take back the billions provided to Pfizer, Moderna etc., all the CovidCon money, ESSER l, ll, lll, etc., as well as Ukraine and the war machine. That might help Social Security just a bit.....just saying!
BigHarma's big lie, "not just nasal cavity or lungs" never could prevent airborne infections because mRNAs spikes are circulating in the blood serum!
That too!
Dr. Yeadon makes this precise point.
This lone point that gets buried in an avalanche of citations and links...seems to explode the whole root lie.
Fascinating stuff!
Magnificent. The drum that I have been beating from the beginning is get to the ROOT lies of the injections.
This is the linchpin to all of it.
Almost.
Great article Andreas. They could have used different protein targets to effective, but they chose the full toxic S spike, with N-terminal domain. Taking in mind, Bill Gates' equation of CO2= PxSxExC. Then suggesting a 10-15% reduction of P with sloppy "vaccines". The FDA's EUA is basically a continuous license to experiment on the human population. And without a method of safely injecting mRNA ( such as, Aspiration before injection), it is known a certain % would enter the blood stream, thus particles traveling to any organ, tissue, brain barrier, would occur. These monsters behind the glass mirror know what is happening, and know every bit of what they did, but don't say anything. That's the crime right there.
Or they could have not created the virus in the first place? But as they did, they think the S spikes are the best tool for the job in reducing P.
of course! from what I could understand, DTRA/DARPA had a scaffolding plan in a phased approach. essentially rapid prototyping of a "vaccine" with the spike pathogen depending on the level of threat. I think this follows with the Monkeypox spike. Plug N Play sort of modules that get integrated into the booster.
Since the "pandemic" started in 2020, I've gotten sick once. Lasted all of three days. Someone close to me on the other hand, who got the shot, has gotten sick more times than I can recall, and usually remains sick for a longer period of time.
“deployed to eek out…”
Or even eke them out.
I appreciate your work, thank you.
I'd like to draw your attention to Eleni Papadopulos-Eleopulos' and her Perth group's work on HIV http://www.theperthgroup.com/
Sadly, Eleni passed away not long ago, this year :(
You can find a lot of her presentations, interviews etc., on line. She did an immense service to humanity that has never been recognised. And, she's not alone in what she says.
(Kennedy mentions them briefly in his new book, the Real Antony Fauxi).
It's worth your time to research it further, I believe.
In March 2020, there was a YouTube video posted from a group led by a curious onlooker, someone outside of the accepted science of the international fear mongers group, that debunked the entire NIH story. They stated that what was being visually presented to us as a virus was in fact an exosome, and that there were numerous possible causes for expressing exosomes. Fear being one of them. The video was removed. I can understand why, because they were correct, and Sir Francis Collins, often pictured holding an exosome model from the liver of a monkey, was lying to all of us idiots who would never question his NIH.
Only we’re not that stupid.
It's interesting... Exosomes look exactly like viruses. Spikes on the outside, membrane and then RNA inside. Exosomes seem to be created by cells when they are trying to take out the trash. Viruses are a seperate microbe which has evolved to be highly specialised in the way it infects and interacts with complex organisms despite not being alive or sentient in any way.
Exosomes are poorly understood, but the incredibly complex world of viruses is apparently well understood. It seems like there may be significant overlap between these two domains.
The simplest explanation is often the best
You should go to that 1st International Conference with a presentation! Miami!
I don't think it would take me all that long to run through the Wikipedia pages for these topics. Wouldn't make a very exciting presentation 🙃
Will be good enough for the inaugural?
I'll just identify as an academic, problem solved!
look up amyloidosis.
I've already been tramautized enough by Walter Chestnut's theories, I don't need even more in depth information. I keep waiting for my friends and family to turn into giant balls of spike induced fibrin
unfortunately most likely it is true.
Yes, weird outlandish projections at the time. One most odd was projecting Russia‘s population to grow. I guess he didn’t see this war coming. The heart of a son of man plans his ways and LORD orders his steps?
yeah well ... here is smt i run into
https://mediaarchives.gsradio.net/rense/special/rense_053022_hr2.mp3
Thanks, very informative! What is this talkshow? Btw, they quote about 30 trillion spikes to be produced by the jabbed, from the general math. So we are about right with what I quoted here, as not every mRNA injected will successfully transfect, and some will transfect in bunches the same cell, reducing the throughput.
Or they didn’t think Russia will accept their jab?
who knows ...
This is excellent. Looking forward to the rest.
Hey dummy - mRNA has never been effective.
The Covid injections are a safe & effective way to commit genocide.
Speaking of Genocide:
"Anthony Fauci, Albert Bourla, Stephane Bancel, alongside many others, charged with charged with Genocide in legal filing with the International Criminal Court (ICC)"
https://ragnarforseti.substack.com/p/anthony-fauci-albert-bourla-stephane?r=hjhbr&s=w&utm_campaign=post&utm_medium=web
Lol. I almost typed the rest too... 'preventing infection or reducing severity ' blah blah...
But I figured everyone would get my point...
It all worked out for the best because now people will see your comment
(which was marvelous)
Speaking of plutonium, read today international 360° possibly...
There were up to 30 or 40 kg? Of plutonium and uranium respectively in the UKraine nuke you lar lab.
But Andreas, will you write up a post about Hunter BidenHo latest and biolabs rung round Russia in UKraine...
I feel like I get the crumbs but missed the big feast on the table, did I¿
What's the big deal! Ukraine gave up so many nukes back in the nineties, in return for the security guarantees from Russia, UK and US, that having 30 or 40kg left over is pocket lint de la pocket lint, comparatively speaking.
Nothing like a pivot, eh? He's horsing around, as am I.
Scratches underarms and howls
I think the next dungeon is ...Azot...?
Hello! One of my readers linked me to this. Thank you for writing it.
Welcome and thanks! Looking forward to your feedback!
I've worked with exosomes for years (they are great for various regenerative medicine applications including restoring internal organs). Since COVID started, we've found exosome therapy is one of the most effective treatments for COVID (acute, long hauler or vaccine injuries) but the exact reason for this has been a bit of a ? for me, and one of the articles you linked to was helpful for filling in some gaps in my understanding. When people put the work to put something together that helps me I like to acknowledge it. Thank you again!
Could you please expand on exosome treatment for long covid? Exactly what is involved? Any chance the long covid symptoms are linked to amyloidosis?
You get them from a good source (they need to come from a mother who was properly screened, I don't find the ones from adult donors work as well) and then inject them intravenously. There are some tricks to getting a better outcome with the injection, but that's beyond the scope of what I could put into writing here. In a few cases, I have seen people have a large improvement in a matter of minutes which still astounds me to witness.
They seem to help a variety of autoimmune conditions (which arguably characterizes long haul covid). I also believe to some extent they turn off the cell danger response:
https://pubmed.ncbi.nlm.nih.gov/23981537/
Thanks! In the meantime, I have found this link: https://pubmed.ncbi.nlm.nih.gov/29625119/
Exosomes effective in combating amyloid-β. May be the key to understanding why exosome regenerative treatment also works for long covid?
We all know about myocarditis now, but I recently read an explanation for why it is happening that made perfect sense to me. I was surprised I hadn't read this earlier. I can't guarantee that it is true, but it sure makes sense to me. It also explains why athletes seem to go down so often these days.
From "The American Thinker":
https://www.americanthinker.com/articles/2022/05/how_the_covid_vaccines_kill.html
The pale-yellow fluid of the Pfizer or Moderna vial contains billions of microscopic fat globs called lipid nanoparticles. Each is an incredibly tiny envelope, used to conceal the novel drug: messenger RNA. Once injected, the combination of nanoparticles and mRNA becomes a well-camouflaged predator.
According to Pfizer’s own data, less than half the nanoparticles stay in the arm where they were injected. Most slip through tiny cracks in muscle tissue and enter the bloodstream. Venous blood speeds them to the heart, which pumps and disperses them to the entire body.
Depending on the level of exercise, from 5 to 25% of these particles wind up in coronary circulation. Why is this important? Consider the rather large number of nanoparticles that must slip into human heart tissue: 50 to 250 million out of each billion that enter the veins of the arm.
Coronary circulation branches into microscopic capillaries that rush nutrients to heart muscle cells. And since the nanoparticles designed by Pfizer and Moderna masquerade as triglycerides, heart muscle cells are apt to snatch them out of circulation as food.
Now imagine the shock for any hard-charging heart cell that engulfs one of these particles. Expecting a meal, the cell unwraps the envelope, and voilà! Freshly unveiled messenger RNA seizes the cell’s protein-generating apparatus, forcing out a known toxin -- the COVID spike protein.
Very soon, with urgent biochemical signals, the afflicted cell telegraphs news of its hijacking to the immune system, which will marshal what it takes to destroy the cell.
An immune-mediated attack on heart muscle cells is, of course, the very essence of myocarditis. Foreign RNA takes control of a cell’s protein production, transforming these cells into enemies of the body, and the immune system converts them into useless scar tissue. The process is irreversible, as heart muscle cells do not regenerate.
Adolescents seem to be in most danger for some reason. Can you explain that?
What's more, LNPs are "radioactive" in their own right: https://www.bitchute.com/video/djgGWArf7szA/
Well, many of the adolescents I know are very active and energetic.
I know I was at that age, compared to now.
But maybe there are some physiological reasons beyond that. But thanks for the link, I will examine it attentively.
I especially like this -- "Now imagine the shock for any hard-charging heart cell that engulfs one of these particles. Expecting a meal, the cell unwraps the envelope, and voilà! Freshly unveiled messenger RNA seizes the cell’s protein-generating apparatus, forcing out a known toxin -- the COVID spike protein."
Which makes sense to me.
The lnp's are trigycerides which are FOOD for where our bodies need energy the most.
injections are starting amyloidosis which has no cure and could manifest itself in few years.
https://www.medicalnewstoday.com/articles/misfolded-spike-protein-could-explain-complicated-covid-19-symptoms
Thanks for that , Swedes rock! https://liu.se/en/news-item/mojlig-mekanism-bakom-gatfulla-symtom-vid-covid-19-upptackt
The only important distinction between the Covid disease and the "vaccination" is that in addition to the S spike code the jab contains about 35-70% of truncated code that may produce truncated, or cut, chunks, of the S spike, so not need to even cut it with the enzymes. Another one is that the translation of mRNA to S spike is also prone to errors and interruptions due to the modifications to the mRNA introduced to increase the spike output. And third, as you have mentioned, much larger number of S spikes all over the organs and tissues, including the brain.
May I ask how do you estimate the number of spike proteins being generated? I have done the estimation myself some time ago but did not write it down and now don't remember what inputs I have used.
thank you for all you are doing
Found this calculation of the number of mRNA in Pfizer (30mcg) and Moderna (100mcg):
Calcul du nombre de molécules d'ARNm dans une dose de vaccin
1. Nous obtenons la séquence nucléotidique précise des ARNm à partir du
site de partage de données académiques github.com: Assemblics-of-putative-SARS-CoV2-spike-encoding-mRNA-sequences-for-vaccincs-BNT-162b2-and-mRN A-1273
2. Nous calculons la masse molaire de chacun des ARNs (voir annexe): BioNTech/Pfizer_BNT-162b2_vaccine: 1341,379 kDa (1.341.379 Da)
Moderna_mRNA-1273_vaccine: 1288,795 kDa (1.288.795 Da)
3. Nous calculons à combien de molécules réelles correspondent les
dosages indiqués (30 microgrammes et 100 microgrammes)
Pfizer : 6.02 10^23 (nombre d'Avogadro) molécules correspondent à 1,341,379 g
30 microgrammes correspondent donc à (6.02 10^23/1,341,379)x 30 x 10^-6 = 1.35 x 10^13
Moderna : 6.02 10^23 (nombre d'Avogadro) molécules correspondent à 1,341,379 g; 100 microgrammes correspondent donc à (6.02 10^23/1,288,795)x 100 x 10^-6 = 4.67 x 10^13
4. Comparaison avec le nombre de virus dans le cas d'infection naturelle: Les nombres ci-dessus sont véritablement astronomiques, quand on sait qu'un
patient est considéré comme très positif avec une valeur de PCR Ct=24, et que
cela correspond à 2.106 virus/ml
L’injection d’une dose de Pfizer délivre donc autant de mRNA de la protéine Spike que ce qui est contenu dans 1.35 × 10^13/( 2 × 10^6) = 0.675 × 10^7𝑚𝑙 de fluide nasal infecté, soit 6750 litres!
Which is 13.5 trillion mRNAs in one Pfizer dose and 46.7 trillion mRNAs in one Moderna dose. Even in just 10% of that is intact, then it's still a trillion or more mRNA molecules per shot.
thanks.
in my humble opinion all efforts should be on amyloidosis.
If you don't mind, I will use this to write a post, with attribution to you, of course?
In the bigger picture, we are in this together.
As to the number of copies, it may be as high as 10,000 per mRNA (https://pubmed.ncbi.nlm.nih.gov/24688849/): ""For [researchers'] corrected data, the median number of proteins translated per mRNA is 9,800 compared to Schwanhausser et al.'s (2011) original estimate of 900 and their second estimate of 2,800. In yeast, the ratio of protein molecules translated per mRNA is 4,200-5,600 (Ghaemmaghami et al., 2003 Lu et al., 2007 BNID 104745, 104185). Given that mammalian cells have a higher protein copy number than yeast (Milo et al., 2010), it is not unreasonable that the ratio in mammalian cells would be higher.""
An average human protein length is being estimated at 400aa. As the S spike in the jab is 1273-1300aa, this is 3X longer. So, from the estimate of 1000-10,000 copies, we can reduce this, at a minimum, to 300 copies of S spikes per mRNA.
This does not take into account that the mRNA in the jab has been translation optimized and pseudouridine-stabilized. So, we have to multiply back 5X-10X. Then, the minimum estimate rises again to 1,500 copies.
So, very conservatively then, 1,000 copies per mRNA - an order of magnitude more than 100 copies per mRNA!
and the 100 number coming from? Considering the spikes are around for 4 months+?
the person saying it was an MIT scientist, not sure how exactly works.
Thanks! I'd like to be able to work out these numbers again. 15-30 billion mRNA LNPs...
this is a good video too shared by jessica rose.
it looks like this will be the huge puzzle of our lives.
https://www.youtube.com/watch?v=7Ohzi-cU_J8
Wow, great insight! But that 100 number should be substantiated somehow. As Pandelis's clots video (https://twitter.com/janiesaysyay/status/1511002069448093696), note the fibrous structure of the clots as testified by the mortician,
and Dr. Rayn Cole's clot images (https://rumble.com/vxeqvu-pathologist-on-ryan-cole-on-the-mystery-blood-clots.html) demonstrate, there were a lot of fibrils generated from the S spikes (https://liu.se/en/news-item/mojlig-mekanism-bakom-gatfulla-symtom-vid-covid-19-upptackt) in the ones that had succumbed. Or maybe these were the people that possessed some particular genetic susceptibility and had a runaway spike-to-clot process? Anyway, as Pandelis reports, systemic amyloidosis may very much be the thing post Covid and esp. post-jab (https://wmcresearch.substack.com/p/why-ray-liotta-and-millions-of-others). And, of course, the Johns Hopkins dude shot down the suggestion right out he gate (https://www.medicalnewstoday.com/articles/misfolded-spike-protein-could-explain-complicated-covid-19-symptoms), JH being part of the core group of eugenicist research institutions.
someone shared this video you might be interested in. it looks legit.
https://twitter.com/janiesaysyay/status/1511002069448093696
Saw that before: https://rumble.com/vxeqvu-pathologist-on-ryan-cole-on-the-mystery-blood-clots.html
makes perfect sense