When evidence is presented from multiple parties that there are lots of problems, like death, with these injections and the regulators do nothing for years how is this explained? The obvious answer is the people running the regulators and thus the senior management at the regulators are both involved in the fraud. It will take time for enough people to accept this depressing reality. We all need to believe our own eyes, and face up to the ugly truth. Some will never face reality, there are a lot of cowards, but there are enough people that want the truth.
Yes! The size and scope and deceptiveness of these authorities, imo, points to much more than just blindness greed, but that of years of secretive planning to intentionally harm much of the world's population. They want control. But control of so many people would be difficult and expensive, but with the advent of AI and robotics, much of the menial tasks for the Authoritarians could be taken care, so, goodbye "useless eaters".
Not just lots of problems, but problem lots too. How bad is my batch becomes what was in my bad batch and why didn't anyone care. Perhaps we will be seeing commercials from law firms advertising for people who received lot xyzz...you may be entitled to compensation.
The most important thing is for people to realize that virology itself is a pseudoscience and that it, along with cancer, is Big Pharma's biggest cash cow, garners the lion's share of funding for scientists and leads doctors astray from learning what the causes of illness actually are...much knowledge about what makes us sick has been hijacked by virology, the go to explanation whenever any symptom we call illness presents itself. And it is the perfect capitalist ploy...same as terrorism. The war on terror, the war on virus...getting people to fear foreign particles and foreign "others" sure is profitable. It also has the affect of rendering people easy to control. whether the military will save us from the foreign terrorist invaders who hijack planes to crash into and destroy America's most symbolic infrastructure or foreign particles that hijack our own cells to destroy the body...both narratives out of the same playbook. The response to each is devastating.. If there is no virus, there is no vaccine needed...but what then is the so-called vaccine and what is its purpose? We might ask that about the trillions spent on war machines ands incursions to thwart so-called terrorists. Both result in deaths of innocents.
My Sister in law has a hysterectomy because there was polyps in the uterus which could be removed but fear of cancer convinced her to have the uterus removed
Great money spinner for the surgeon
The patient is left with no support for the bowel and bladder
So sorry. I know of people who had their breasts remove because doctors told them they were genetically predisposed. And this was before any precancerous or cancerous changes were discovered. It's criminal
It’s gonna be the source of the “blobs.” At least I’m betting so. Yes, to the long rubbery casts being made inside veins and arteries, but I also think the blobs in the lab-draws are gonna be “silky.”
Spider webs growing in veins? I wonder why traditional blood clotting drugs don't seem to break them up? So they are most likely silk, Collagen, or Fibroin. This is a bit insane.
Hi Kevin, it's Janiesaysyay. Great work! Thought about this, and find it hard to believe human cells could express any protein similar to silk. We don't have the biochemistry. We don't have silk glands like spiders.
However the collagen is VERY interesting because it would aid in the clotting with the LNPs and PEG with blood proteins to form hydrogels.
This is so exciting, so cool you came out with this in the scary season of Halloween. You need a nickname for this, like they do on the Simpsons, Kevin "ScaryCatz" Mckernan, or something like that.
I'm hoping you can now time all of your reveals as themed events. Or we could just continue with the horror them, which seems fitting.
There seems to be a fundamental confusion here about protein names. The mysterious ORF seems to have no resemblance to any silk protein. It’s name MaSp1 seems to have been automatically assigned to the entry G1Y380_9PROT in the Uniprot database (see entry of the gene AZA_01309), and was - for whatever reason - automatically spelt out as „Major ampullate spidroin 1“. Note that this entry has not been reviewed yet. Also, it is interesting that there are other proteins with the abbreviated name MASP1, called „Mannan-binding lectin serine protease 1“. Neither these nor the spidroins line up when checked against the mysterious ORF. So, to conclude, there is presumably no intent of sneaking an amyloidogenic spider silk protein into the vaccine. It’s potential amyloidigenicity, nonetheless, is of great concern!
It’s the template switching potential shown in the Moderna T7 polymerase paper that leads me to believe the poor RIN plots are likely chimeric cis template switches and we have amyloid potential.
Otherwise, I don’t see a Kozak or any ribosomal binding sites to suggest that ORF will get transcribed or translated.
Would have to be a template switch that is expressed from the spike Kozak.
This is sci fi craziness. These murderers have outdone themselves. Silk like proteins. Dr Ardis has already said synthetic peptides mimicking snake and snail toxins were used. Now this.....
While I'm not able to follow the science, the gist of this scenario
suggests to me 3 possibilities -
1) Slipshod omissions or carelessness motivated by greed,
impatience and immunity
2) Pfizer knew exactly what they were doing but omitted or glossed over the presence of certain substances as part of a multi--front attack on the human genome.
3) By prearrangement, Pfizer brought the preparation up to a certain stage of completion, at which time it was turned over to Eugeneshits' (or government?) scientists who worked it further with the
unmentioned/glossed-over substances, then returned it to Pfizer,
whose umbrella of immunity would smooth the bumps and wrinkles
if they were discovered.
While Pfizer may or may not have been told what was done to the preparation, (buyer's preference) there is a good chance they were told, given the fallback mumbo-jumbo used to explain or dismiss
No comments about Curevac yet... So i'll SV-promoter it right here
2020/11/10
"Elon Musk confirmed that Tesla is currently working on version 3 of its vaccine printer for CureVac and he believes that it is going to be an “important product for the world.” · Earlier this year, Musk announced that Tesla has become the manufacturing partner for biotech firm CureVac"
Silk is a really amazing substance but i do not want to grow this in me even if it sjoots out only out of my hands like Spiderman. But here it seems its grown inside of us being indistructable with clot dissolving agents. They say its to make a form of hydrogel which 8s used to integrate nanotech with our human tissues badocally to bind it to glue it.
The similar proteins are only around 25-30% identical from what I can tell from your photo. The proteins that are similar are also never really in a string or line, but dispersed as single or double matches. Trying to figure out UNIPROT now so I can look at the full sequence alignments. I'm not personally going to postulate on amyloidogenic potential with that amount of similarity, but it's certainly possible. What I find more shocking, is just how big of a mystery that thing is. Injecting DNA with a viable mystery open reading frame, that is housed in a high half life LNP and ready to transfect cells in multiple locations within the body, into billions of people, is batshit crazy. Might be better, since it's an unknown protein, to assess lots of on record amyloidogenic sequences, and manually search the mystery protein for them? I have a feeling UNIPROT would have found those though... Or, if anyone has access, there is likely software that determines amyloidogenic potential, that the mystery sequence can be fed into. I know they exist for the prion like domains, one was used here https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878784/pdf/microorganisms-10-00280.pdf
If such software exists for amyloidogenic potential, it may help answer the mystery protein's role, if any, as a contributor or main cause of clots
I should have figured you'd know exactly what software to use already :P
I'm assuming the "self assembly" part refers to their potential for those regions to cause a misfold and become fibrous formations? Perhaps the multi alanine regions are actually an issue.... 6-12 form beta pleated sheets in normal spidroins, and amyloids generally form from "beta pleated sheets aggregating into long fibers". The mystery protein is chock full of them, though I haven't checked the Pizer spike. Even if it's not the G's and A's, the regions the software is identifying must have very high potential for misfolding into beta pleated sheet aggregations. Not sure why the potential is the same with double the regions though... Regardless, just to see how common this is, I just stuffed a random influenza hemagglutinin in there (Influenza's spike, also a class 1 fusion viral protein, should also be in two subunits that get cleaved, with the top subunit being a fusion suppressive cap, very similar structure). There is no amyloidogenic potential in the entire protein that goes anywhere near the cutoff point, score was zero for it https://www.genome.jp/entry/vg:1460996 (provided I did it right, just copy pasted the reference genome into the software). Also tried gp160 from an HIV genome https://www.genome.jp/entry/vg:1490007
And again, no amyloidogenic potential in any region anywhere near 0.5, unless I entered the sequence incorrectly. This does not appear to be very common in the viral world at first glance, making it even more suspicious (Which makes sense. A viable viral protein would be good at maintaining its intended confirmations, not misfolding into fibrous crap all the time).
This is so weird. Why pick a protein with this much potential as the target? Why create a viable ORF with similar potential through codon optimization? The only options are: The people making these things are absolute hacks, and didn't even check basic risks like these, or, some puppet master somewhere, intentionally wants people making these risky proteins. Either way, it shows us a massive failure on the part of regulatory bodies that are supposed to be vetting these things, especially when we take the contamination into account as well. Disturbing to say the least. I appreciate you providing the software, thanks for your time
Yeah I know I saw the software output. I meant in relation to the alanine and glycine quantity. The literature seems to attribute at least the alanine repeats to beta pleated sheets in spidroins, and the mystery protein has a lot of it. I'm also pretty sure something called "glycine zippers" are a folding issue, but going off memory with that one. As such, I was wondering if the amyloidogenic regions from the software output, could be referenced back to the amino acids in those regions of the mystery protein, then compared to the Pfizer spike, to see if those regions are also A or G heavy. I didn't elaborate well, my bad, everything is always so long winded I try to condense to the detriment of the topic sometimes.
Why are people and scientists surprised? Pfizer paid the largest FDA criminal fine in history. People let a criminal inject an unknown EUA substance into their body. Now THAT is bat shit crazy. I am shocked so many people complied, and are still complying.
To me it's that.... It seems so amateur. Like almost excessively so, I don't see how they could really not understand they would be figured out eventually. It's hard for me to find motive for this level of incompetence, I can't see how not trying to do a better job vetting your sequences and DNA removal methods would be less costly in the long run, especially if you lost immunity because you altered something. Maybe I just don't understand the economics behind cutting those corners though. Idk, it's like I'm witnessing morons attempt to commit scientific fraud. Only issue is these morons make tons of medicine for the global population, so I have trouble seeing how they could be THIS stupid. Could also be I'm just naïve.
I didn't even think of this. It should have been obvious. The amino acid chain is too long, the probability is very small a chain that long would be accidentally created without a stop codon popping up somewhere by pure chance. Idk wtf that thing is, but chances are more likely it was placed there on purpose than on accident.
The intention was to kill! That is why the scare tactics involved. It didn't matter down the track who found out as all are patsys and in one way or another they the perpetrators will end up dead. Definitely done by the deranged.
"Major ampullate spidroins are large proteins with an extension of 250-350 kDa, with an average of 3500 amino acids. They represent a polymeric organization, mostly based on highly homogenized tandem repeats. There are 100 tandem copies of 30 to 40 amino acids which repeat sequence and they represent more than 90% of the protein sequence.[5] Alanine and glycine residues are the most abundant amino acids in these proteins. Alanine appears in blocks of six to fourteen units that form β-sheets. These alanine blocks can stack to create crystalline structures in the fiber, linking different protein molecules together. Glycine is present in different motifs, such as GGX and GPGXX (where X = A, L, Q, or Y), that also have specific secondary structures (3 10 helix and β-spiral, respectively). Glycine-rich regions are more amorphous and contribute to extensibility and flexibility."
While the A regions aren't 6-14 long, I'm seeing a lot of A's next to each other, a lot of G's, and what looks like high content for both, though I haven't calculated exact percentages (in the mystery protein above). Also, the paper you posted indicates the N terminal domain has the highest amyloid potential for Spidroin, so perhaps comparing that region to the mystery protein would also help shed light on the issue
Thanks for standing strong on this and your excellent work to provide accurate science based research and information. I do not have enough words to express my thankfulness and gratitude.
Isaiah 59:5-6 They hatch cockatrice' eggs, and weave the spider's web: he that eateth of their eggs dieth, and that which is crushed breaketh out into a viper. 6 Their webs shall not become garments, neither shall they cover themselves with their works: their works are works of iniquity, and the act of violence is in their hands.
Opens up the whole barn door of lawsuits stripping away the vaccine companies protection instead of them getting protection because of the news of leaving out information to FDA
as I remember Robert F Kennedy Jr stated in one his posts they have protection as long as they show transparency to the regulators that’s a so graciously call them I think it was in 76 or so they signed off as long as they told FDA everything that was in the vaccines and the possible side effects they were protected against lawsuits
Oh interesting. As long as they tell fda potential side effects they are protected. Is that why the list of side effects in that PowerPoint slide presented to FDA in Nov 2020 right before rollout, is so very very very lengthy? It’s just CYA not anything that they really know of? This is just sick. 1986 liability protection law needs to be repealed!!
Yes Patti and when big Pharma went to Reagan to plead to them that they need Libel protect , to Reagan’s credit he said why don’t you just make them safe and big Pharma response was we can’t make them safe hence the 1986. liability act
Something to silk. I was advised to get rid of my trigeminal neuralgia to drill a little hole into my skull and then glue an offending twisted bloodvessel away from the trigeminal nerve to my skull via SILK STRANDS. So this seems to be already used in medicine to glue and tie bloodvessels gently to other tissues. But to express it is different.
Promoter region remain transcriptionally active in human cells and 2) the constitutive transport element (CTE) expression in the target cells aids the facilitation of the nuclear export for the gene therapy
When evidence is presented from multiple parties that there are lots of problems, like death, with these injections and the regulators do nothing for years how is this explained? The obvious answer is the people running the regulators and thus the senior management at the regulators are both involved in the fraud. It will take time for enough people to accept this depressing reality. We all need to believe our own eyes, and face up to the ugly truth. Some will never face reality, there are a lot of cowards, but there are enough people that want the truth.
Yes! The size and scope and deceptiveness of these authorities, imo, points to much more than just blindness greed, but that of years of secretive planning to intentionally harm much of the world's population. They want control. But control of so many people would be difficult and expensive, but with the advent of AI and robotics, much of the menial tasks for the Authoritarians could be taken care, so, goodbye "useless eaters".
Not just lots of problems, but problem lots too. How bad is my batch becomes what was in my bad batch and why didn't anyone care. Perhaps we will be seeing commercials from law firms advertising for people who received lot xyzz...you may be entitled to compensation.
We are out there. Isolated. But committed to the truth for those we care for. One person at a time right now.
The most important thing is for people to realize that virology itself is a pseudoscience and that it, along with cancer, is Big Pharma's biggest cash cow, garners the lion's share of funding for scientists and leads doctors astray from learning what the causes of illness actually are...much knowledge about what makes us sick has been hijacked by virology, the go to explanation whenever any symptom we call illness presents itself. And it is the perfect capitalist ploy...same as terrorism. The war on terror, the war on virus...getting people to fear foreign particles and foreign "others" sure is profitable. It also has the affect of rendering people easy to control. whether the military will save us from the foreign terrorist invaders who hijack planes to crash into and destroy America's most symbolic infrastructure or foreign particles that hijack our own cells to destroy the body...both narratives out of the same playbook. The response to each is devastating.. If there is no virus, there is no vaccine needed...but what then is the so-called vaccine and what is its purpose? We might ask that about the trillions spent on war machines ands incursions to thwart so-called terrorists. Both result in deaths of innocents.
FEAR is the weapon
My Sister in law has a hysterectomy because there was polyps in the uterus which could be removed but fear of cancer convinced her to have the uterus removed
Great money spinner for the surgeon
The patient is left with no support for the bowel and bladder
So sorry. I know of people who had their breasts remove because doctors told them they were genetically predisposed. And this was before any precancerous or cancerous changes were discovered. It's criminal
"..we shouldn't have to do this...." true. Glad you are though!
It’s gonna be the source of the “blobs.” At least I’m betting so. Yes, to the long rubbery casts being made inside veins and arteries, but I also think the blobs in the lab-draws are gonna be “silky.”
Fascinating stack, Kevin!
Spider webs growing in veins? I wonder why traditional blood clotting drugs don't seem to break them up? So they are most likely silk, Collagen, or Fibroin. This is a bit insane.
Hi Kevin, it's Janiesaysyay. Great work! Thought about this, and find it hard to believe human cells could express any protein similar to silk. We don't have the biochemistry. We don't have silk glands like spiders.
However the collagen is VERY interesting because it would aid in the clotting with the LNPs and PEG with blood proteins to form hydrogels.
I doubt it’s making silk but if it does make a protein is likely amyloidogenic.
I updated the bottom of the post with AmyloGram predictions of the peptide.
AWESOME, thanks so much!
This is so exciting, so cool you came out with this in the scary season of Halloween. You need a nickname for this, like they do on the Simpsons, Kevin "ScaryCatz" Mckernan, or something like that.
I'm hoping you can now time all of your reveals as themed events. Or we could just continue with the horror them, which seems fitting.
There seems to be a fundamental confusion here about protein names. The mysterious ORF seems to have no resemblance to any silk protein. It’s name MaSp1 seems to have been automatically assigned to the entry G1Y380_9PROT in the Uniprot database (see entry of the gene AZA_01309), and was - for whatever reason - automatically spelt out as „Major ampullate spidroin 1“. Note that this entry has not been reviewed yet. Also, it is interesting that there are other proteins with the abbreviated name MASP1, called „Mannan-binding lectin serine protease 1“. Neither these nor the spidroins line up when checked against the mysterious ORF. So, to conclude, there is presumably no intent of sneaking an amyloidogenic spider silk protein into the vaccine. It’s potential amyloidigenicity, nonetheless, is of great concern!
Couldn’t agree more.
The blast scores are weak.
It’s the template switching potential shown in the Moderna T7 polymerase paper that leads me to believe the poor RIN plots are likely chimeric cis template switches and we have amyloid potential.
Otherwise, I don’t see a Kozak or any ribosomal binding sites to suggest that ORF will get transcribed or translated.
Would have to be a template switch that is expressed from the spike Kozak.
The alien gene in jab converts/ transcribes your cells to learn how to do this! Hybrid human making foreign proteins 😡😢😡
This is sci fi craziness. These murderers have outdone themselves. Silk like proteins. Dr Ardis has already said synthetic peptides mimicking snake and snail toxins were used. Now this.....
While I'm not able to follow the science, the gist of this scenario
suggests to me 3 possibilities -
1) Slipshod omissions or carelessness motivated by greed,
impatience and immunity
2) Pfizer knew exactly what they were doing but omitted or glossed over the presence of certain substances as part of a multi--front attack on the human genome.
3) By prearrangement, Pfizer brought the preparation up to a certain stage of completion, at which time it was turned over to Eugeneshits' (or government?) scientists who worked it further with the
unmentioned/glossed-over substances, then returned it to Pfizer,
whose umbrella of immunity would smooth the bumps and wrinkles
if they were discovered.
While Pfizer may or may not have been told what was done to the preparation, (buyer's preference) there is a good chance they were told, given the fallback mumbo-jumbo used to explain or dismiss
the ingredients in question.
3
All of the above.
No comments about Curevac yet... So i'll SV-promoter it right here
2020/11/10
"Elon Musk confirmed that Tesla is currently working on version 3 of its vaccine printer for CureVac and he believes that it is going to be an “important product for the world.” · Earlier this year, Musk announced that Tesla has become the manufacturing partner for biotech firm CureVac"
The fibrous clots have a similarity to silk? People have webs growing in their veins as a result of this mystery ORF? Pretty creepy.
Silk is a really amazing substance but i do not want to grow this in me even if it sjoots out only out of my hands like Spiderman. But here it seems its grown inside of us being indistructable with clot dissolving agents. They say its to make a form of hydrogel which 8s used to integrate nanotech with our human tissues badocally to bind it to glue it.
The similar proteins are only around 25-30% identical from what I can tell from your photo. The proteins that are similar are also never really in a string or line, but dispersed as single or double matches. Trying to figure out UNIPROT now so I can look at the full sequence alignments. I'm not personally going to postulate on amyloidogenic potential with that amount of similarity, but it's certainly possible. What I find more shocking, is just how big of a mystery that thing is. Injecting DNA with a viable mystery open reading frame, that is housed in a high half life LNP and ready to transfect cells in multiple locations within the body, into billions of people, is batshit crazy. Might be better, since it's an unknown protein, to assess lots of on record amyloidogenic sequences, and manually search the mystery protein for them? I have a feeling UNIPROT would have found those though... Or, if anyone has access, there is likely software that determines amyloidogenic potential, that the mystery sequence can be fed into. I know they exist for the prion like domains, one was used here https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878784/pdf/microorganisms-10-00280.pdf
If such software exists for amyloidogenic potential, it may help answer the mystery protein's role, if any, as a contributor or main cause of clots
It is a weak E-Value.
I did update the bottom of the stack to include AmyloGram prediction.
It looks like a similar amyloid potential as Pfizer spike but has many more (~2X) residues capable of it.
http://biongram.biotech.uni.wroc.pl/AmyloGram/
I should have figured you'd know exactly what software to use already :P
I'm assuming the "self assembly" part refers to their potential for those regions to cause a misfold and become fibrous formations? Perhaps the multi alanine regions are actually an issue.... 6-12 form beta pleated sheets in normal spidroins, and amyloids generally form from "beta pleated sheets aggregating into long fibers". The mystery protein is chock full of them, though I haven't checked the Pizer spike. Even if it's not the G's and A's, the regions the software is identifying must have very high potential for misfolding into beta pleated sheet aggregations. Not sure why the potential is the same with double the regions though... Regardless, just to see how common this is, I just stuffed a random influenza hemagglutinin in there (Influenza's spike, also a class 1 fusion viral protein, should also be in two subunits that get cleaved, with the top subunit being a fusion suppressive cap, very similar structure). There is no amyloidogenic potential in the entire protein that goes anywhere near the cutoff point, score was zero for it https://www.genome.jp/entry/vg:1460996 (provided I did it right, just copy pasted the reference genome into the software). Also tried gp160 from an HIV genome https://www.genome.jp/entry/vg:1490007
And again, no amyloidogenic potential in any region anywhere near 0.5, unless I entered the sequence incorrectly. This does not appear to be very common in the viral world at first glance, making it even more suspicious (Which makes sense. A viable viral protein would be good at maintaining its intended confirmations, not misfolding into fibrous crap all the time).
Tried the spike on 229E too just now, so I could be closer to the virus family in question. Also nothing https://www.genome.jp/entry/vg:918758
This is so weird. Why pick a protein with this much potential as the target? Why create a viable ORF with similar potential through codon optimization? The only options are: The people making these things are absolute hacks, and didn't even check basic risks like these, or, some puppet master somewhere, intentionally wants people making these risky proteins. Either way, it shows us a massive failure on the part of regulatory bodies that are supposed to be vetting these things, especially when we take the contamination into account as well. Disturbing to say the least. I appreciate you providing the software, thanks for your time
I did check the Pfizer spike and it’s also amyloidogenic but it has half as many residues as the mystery ORF. It’s at the bottom of the sstack.
Yeah I know I saw the software output. I meant in relation to the alanine and glycine quantity. The literature seems to attribute at least the alanine repeats to beta pleated sheets in spidroins, and the mystery protein has a lot of it. I'm also pretty sure something called "glycine zippers" are a folding issue, but going off memory with that one. As such, I was wondering if the amyloidogenic regions from the software output, could be referenced back to the amino acids in those regions of the mystery protein, then compared to the Pfizer spike, to see if those regions are also A or G heavy. I didn't elaborate well, my bad, everything is always so long winded I try to condense to the detriment of the topic sometimes.
Why are people and scientists surprised? Pfizer paid the largest FDA criminal fine in history. People let a criminal inject an unknown EUA substance into their body. Now THAT is bat shit crazy. I am shocked so many people complied, and are still complying.
To me it's that.... It seems so amateur. Like almost excessively so, I don't see how they could really not understand they would be figured out eventually. It's hard for me to find motive for this level of incompetence, I can't see how not trying to do a better job vetting your sequences and DNA removal methods would be less costly in the long run, especially if you lost immunity because you altered something. Maybe I just don't understand the economics behind cutting those corners though. Idk, it's like I'm witnessing morons attempt to commit scientific fraud. Only issue is these morons make tons of medicine for the global population, so I have trouble seeing how they could be THIS stupid. Could also be I'm just naïve.
Nevermind. This open reading frame is probably on purpose
https://nitter.net/ImmunoGangsta/status/1721368902473568518#m
I didn't even think of this. It should have been obvious. The amino acid chain is too long, the probability is very small a chain that long would be accidentally created without a stop codon popping up somewhere by pure chance. Idk wtf that thing is, but chances are more likely it was placed there on purpose than on accident.
The intention was to kill! That is why the scare tactics involved. It didn't matter down the track who found out as all are patsys and in one way or another they the perpetrators will end up dead. Definitely done by the deranged.
"Major ampullate spidroins are large proteins with an extension of 250-350 kDa, with an average of 3500 amino acids. They represent a polymeric organization, mostly based on highly homogenized tandem repeats. There are 100 tandem copies of 30 to 40 amino acids which repeat sequence and they represent more than 90% of the protein sequence.[5] Alanine and glycine residues are the most abundant amino acids in these proteins. Alanine appears in blocks of six to fourteen units that form β-sheets. These alanine blocks can stack to create crystalline structures in the fiber, linking different protein molecules together. Glycine is present in different motifs, such as GGX and GPGXX (where X = A, L, Q, or Y), that also have specific secondary structures (3 10 helix and β-spiral, respectively). Glycine-rich regions are more amorphous and contribute to extensibility and flexibility."
https://en.wikipedia.org/wiki/Spidroin
While the A regions aren't 6-14 long, I'm seeing a lot of A's next to each other, a lot of G's, and what looks like high content for both, though I haven't calculated exact percentages (in the mystery protein above). Also, the paper you posted indicates the N terminal domain has the highest amyloid potential for Spidroin, so perhaps comparing that region to the mystery protein would also help shed light on the issue
Thanks for standing strong on this and your excellent work to provide accurate science based research and information. I do not have enough words to express my thankfulness and gratitude.
Silk-fibroin used for tissue engineering: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218181/
Isaiah 59:5-6 They hatch cockatrice' eggs, and weave the spider's web: he that eateth of their eggs dieth, and that which is crushed breaketh out into a viper. 6 Their webs shall not become garments, neither shall they cover themselves with their works: their works are works of iniquity, and the act of violence is in their hands.
Only one in a Billion would be affected by sv40 genome...
...except they injected Billions into each victim
Very incisive piece!
Opens up the whole barn door of lawsuits stripping away the vaccine companies protection instead of them getting protection because of the news of leaving out information to FDA
as I remember Robert F Kennedy Jr stated in one his posts they have protection as long as they show transparency to the regulators that’s a so graciously call them I think it was in 76 or so they signed off as long as they told FDA everything that was in the vaccines and the possible side effects they were protected against lawsuits
Oh interesting. As long as they tell fda potential side effects they are protected. Is that why the list of side effects in that PowerPoint slide presented to FDA in Nov 2020 right before rollout, is so very very very lengthy? It’s just CYA not anything that they really know of? This is just sick. 1986 liability protection law needs to be repealed!!
Yes Patti and when big Pharma went to Reagan to plead to them that they need Libel protect , to Reagan’s credit he said why don’t you just make them safe and big Pharma response was we can’t make them safe hence the 1986. liability act
Totally agree with you
Something to silk. I was advised to get rid of my trigeminal neuralgia to drill a little hole into my skull and then glue an offending twisted bloodvessel away from the trigeminal nerve to my skull via SILK STRANDS. So this seems to be already used in medicine to glue and tie bloodvessels gently to other tissues. But to express it is different.
I was just holding the beer but i didnt really drink it. This is how the fact checkers talk which are more like pharma defenders.
Reminds me on Clinton. I didnt inhale lol. They are all the same. Liars.
Clinton didn't inhale. He just had an oral fixation...😁
Mason-Pfizer Simian Retro Virus renamed
Promoter region remain transcriptionally active in human cells and 2) the constitutive transport element (CTE) expression in the target cells aids the facilitation of the nuclear export for the gene therapy
https://en.wikipedia.org/wiki/Mason-Pfizer_monkey_virus
The ssRNA virus appears sporadically in mammary carcinoma of captive macaques at breeding facilities which expected as the natural host