Have a look at the Social Security savings and estate tax acceleration. Replacing this demographic with immigrants you eventually naturalize and tax could wipe out trillions in debt.
Ok..the replacement theory of one demographic with another ..might..might wipe out debt levels.We should be seeing this in Europeans countries then.We see the reverse.
Yes.It was rhetorical.Which means the US (alone in the world)can achieve this since by implication it doesn`t have this welfare state.Okay..then the more illegal and legal immigrants into the US...will increase the chance of wiping out trillions in debt....okay...then open the borders and require no criteria for moving there and have no restrictions on people moving there should lead to a financial paradise...good luck with that !!..so far looking at most indicators..your population is going backwards in most indicators whilst the top % gets wealthier and the industrial/pharma complex gets wealthier..magical thinking will save you for sure !
This is interesting but very technical and we know that, "these people" will always deny any possibilities of yet-unknown harms. So expecting the worst is pretty rational.
I'd like to know if unvaxed show signs of "spike" or whatever the new protein is actually. What if these rouge plasmids spread somehow.
There is a smell everywhere and it's not a natural smell. It's coming from people. A separate subject but it's been around since the shots and it's not going away. Something inside of people is creating this, I believe.
My wife is well vaxed and I don’t like sleeping with her anymore. It is vibrational, auric I suppose. There may be a smell factor but I haven’t consciously noticed it
Interesting. I have noticed subtle changes in some people I know who are also full of the shots...sort of a coldness...hopefully your wife hasn't got that.
The smell is a real thing....I go into a store, usually I can smell it before I walk through the doors...the intensity varies. Sometimes I smell it walking past a house or in a shopping area. Some materials absorb it...clothing, paper and so spread whatever it is to us all.
I made some videos earlier this year talking about it. I had a few people comment that they smell something too. One person said the vaxxed family member they live with smells so bad they have to sleep and mostly stay on the other side of the house. The best description given for what it smells like was "dryer sheets" but that's not where it's coming from.
I am a lay person trying to improve my understanding of the context of what's being discussed here. If "these plasmids in fact make spike RNA", does that happen by the promoters and/or enhancers reverse transcribing the code for the spike into the DNA of the cell, after which there is ongoing, ordinary expression of that code (involving RNA of course) and production of spike proteins? Or is there some other way in which the plasmids might make spike RNA? Thanks in advance.
Here is how it would happen in plain language. Vials are contaminated with residual DNA plasmids that contain the reverse transcribed mRNA that codes for the spike protein. The injected LNPs would therefore contain the mRNA for the spike protein but also contain DNA plasmids that have the reverse transcribed spike protein sequence in DNA form. When the LNP enters the cytoplasm of the cell, it breaks open and releases the mRNA and the DNA plasmid contaminant. The DNA that codes for the spike protein could, with promoters, become incorporated into the genome of that cell. When that cell transcribes mRNA from its DNA to make proteins, it could send out from its nucleus, mRNA that codes for the spike protein. So, we get persistent spike proteins that are coded for by the cell, not by the injected mRNA.
"So this risk cannot be ruled out. Ultimately, one needs RNA-Seq data from these plasmids transfected in mammalian cells without the modRNA to see if these plasmids in fact make spike RNA. If they do, then that might explain persistent spike expression in patients. Once RNA is made, it already has the proper Kozak sequences to initiate translation in mammalian cells."
**********************
This seems to me to outline an approach to testing the hypothesis that contaminant plasmids in the mRNA "vaccines" may initiate "persistent spike expression in patients".
A persistent question for many of us is: "I'd like to know if unvaxed show signs of "spike" or whatever the new protein is actually. What if these rouge [rogue] plasmids spread somehow." (TheFrontPorchMedia, above)
(The pathology of PACS is of course an ongoing problem.)
I’m not sure if my question went through. Is it true that testing for the persistent spike proteins can only be done through research level testing? The everyday type of testing is not adequate?
The problem right now is that there is no way to reliably and affordably test for spike proteins in the blood directly. There is a lab in Germany that claims to be able to do it, http://Inmodia.de, but it is expensive. I had a recent discussion with Dr. Mark Trozzi MD, http://Dr.Trozzi.org, who is confident we will have a reliable method soon in the US and Canada. The testing we do now is measuring spike antibodies, an indirect way of estimating spike protein levels.
"Vials are contaminated with residual DNA plasmids that contain the reverse transcribed mRNA that codes for the spike protein."
this does not sound logical, to me. A DNA plasmid should have DNA building blocks, not mRNA... Maybe what you mean here is the DNA plasmid encodes DNA sequence of the reverse transcribed Spike? If so, a reverse sequence would be incorporated with this gene 'therapy' into the human genome, not the one of the Spike.. Since the mod mRNA is recognized by the human ribosome, one can also suspect, a reverse transcription of that construct directly is also possible. That would give the 'normal Spike', not the reversed one.
The issues are always around the presence of the polymerases, one recognizing DNA and making its copy into mRNA, the other ('viral' one) reading RNA and making DNA out of it. And then we also have what SARS-CoV2 has, RdRp, RNA dependent RNA polymerase... The head is now spinning, in my case.
Truly speaking I'm kind of lost in the entire production 'procedure' but want to learn how it really works... Just sorry for the c-on-fusion.
And the guru of all, on this topic, David Baltimore, just died.., with 87.
“Maybe what you mean here is the DNA plasmid encodes DNA sequence of the reverse transcribed Spike?” Yes, that’s right. When the DNA sequence gets integrated, the nucleus can transcribe spike encoding mRNA from it. The spike encoding mRNA leaves the nucleus, and ribosomes will use that to make (translate) the spike protein.
Thanks Kevin (another one, just noticing;)), WAITED for that response AND the confirmation..
Also your other comment says:"The problem right now is that there is no way to reliably and affordably test for spike proteins in the blood directly. "
if so, how on earth every single blood test lists countless SINGLE proteins (albumin, globulin, etc., etc.) all related to many different diseases????
The biochemistry has all the tools they can to detect ANY protein, in particular such a lethal and toxic like Spike... Here one simple example:
So 'they' just DON'T DO it on PURPOSE, I do believe. Imagine scientists would detect ONLY the -PP- molecular clone of Spike in everyone. What would that mean??? We are all sick because of the injections only AND shedding of the toxic Spike from the injections only or the genetic material itself(equally from the injections only!!), with the latter I hope a LOT not being the case.
Oh, and there would be many ways to do that detection, btw. using exactly the same PCR test looking for JUST The specific, unique pieces of the Spike, like that region having the -PP- mutation I mentioned...
Optimizing Snyder’s setup to detect only spike protein is technically feasible and would reduce cost, labor, and analysis time. But even optimized, it is still far from inexpensive or simple enough for routine clinical or home testing. Currently, detection of vaccine-derived spike protein remains a high-sensitivity, specialized, and expensive lab task.
actually with your response, one more thought, about the possibility of incorporation of the reverse Spike sequence in nucleaus... A reverse Spike mRNA relative to the injected mod mRNA of Spike, after crossing the nucleus would mean a high probability of 'neutralisation'/silencing, or Spike fragments or the entire protein... Since many of the diseases come exactly from these fragments, anything what would initiate that silencing, would 'heal' the disease. Is that the big 'cure the cancer' advertisement?? Just a fantasy...
Sorry for any confusion on this topic. The reverse transcription is just a lab tool to replicate the mRNA, not to “reverse” the protein itself. If that reverse transcribed DNA got integrated into human DNA, the resulting mRNA would still make the same spike protein — it would not be reversed or ‘backwards’.
Try as they may, there is no way to remove DNA contaminants from any shots called vaccines, including traditional childhood shots that do not use mRNA technology, or do not use DNA plasmids. DNA is always in there because of the media they grow it in. It could be animal DNA. It could be human DNA. I've been warning about this since 1984 when I first became aware of it.
"This is less clear that such an RNA would be translated in bacterial cells as it would require Shine-Dalgarno sequences in the RNA to attract bacterial ribosomes."
-> why do the injections knock out mainly one type of bacterial species, the bifidos?
The attention to the methylation sites tracking, reminds me of these news today:
"TruDiagnostic Wins $321K NIH Grant for Epigenetic-Based Disease Modeling Tech" with the quote:
"NEW YORK — TruDiagnostic said Tuesday that it has received a $320,511 grant from the National Institutes of Health to develop a system for disease modeling using epigenetic markers.
Called the W-Function Epigenomic Roadmap, the system will map DNA methylation changes to provide insights into disease onset, progression, and response to treatment, according to the Lexington, Kentucky-based company."
So these cryptic promoters are like IRESes in mRNA?
There was some talk in the beginning about the mRNA having unknown IRES sites. At RiboClub Canada last year, there was a presentation about IRES sites in 3'UTR that could make 2 proteins from the same mRNA.
I don't know if my previous message went through. your pictures made me think of Barbara Newhall Follett. A brilliant precocious young woman, with a sensibility close to yours (I think).She led a charmed and strange life. I greatly respect you and what you do.
We were all reassured that the carrying capacity of the LNPs was not much more than two modRNA transcripts, can one cram a full length pcDNA into an LNP ~90nm diameter?
You post actual single molecule Nanopore sequences and jackasses still jump on these threads saying Nutuhn.
That didn’t happen. It’s all fake and I’m so sure of myself because some no virus loons told me so!
Instablock
Don't ever be unsure of yourself. You got this.
Mistakes weren’t made , it was to depopulate.
Its a "cool meme" if you ignore the "data"...
Killing off mostly people over the age of 60 will sure effect birth rates..oh hang on..
It doesnt..
https://www.worldometers.info/world-population/
Have a look at the Social Security savings and estate tax acceleration. Replacing this demographic with immigrants you eventually naturalize and tax could wipe out trillions in debt.
Ok..the replacement theory of one demographic with another ..might..might wipe out debt levels.We should be seeing this in Europeans countries then.We see the reverse.
There is a Substack I have on this.
When climbing the Bradford hill.
You should read it.
I’m not going redebate this in text.
Because euro countries have welfare programs that pay enough money one doesn't need to work.
Yes.It was rhetorical.Which means the US (alone in the world)can achieve this since by implication it doesn`t have this welfare state.Okay..then the more illegal and legal immigrants into the US...will increase the chance of wiping out trillions in debt....okay...then open the borders and require no criteria for moving there and have no restrictions on people moving there should lead to a financial paradise...good luck with that !!..so far looking at most indicators..your population is going backwards in most indicators whilst the top % gets wealthier and the industrial/pharma complex gets wealthier..magical thinking will save you for sure !
Strawman
This is interesting but very technical and we know that, "these people" will always deny any possibilities of yet-unknown harms. So expecting the worst is pretty rational.
I'd like to know if unvaxed show signs of "spike" or whatever the new protein is actually. What if these rouge plasmids spread somehow.
There is a smell everywhere and it's not a natural smell. It's coming from people. A separate subject but it's been around since the shots and it's not going away. Something inside of people is creating this, I believe.
My wife is well vaxed and I don’t like sleeping with her anymore. It is vibrational, auric I suppose. There may be a smell factor but I haven’t consciously noticed it
Interesting. I have noticed subtle changes in some people I know who are also full of the shots...sort of a coldness...hopefully your wife hasn't got that.
The smell is a real thing....I go into a store, usually I can smell it before I walk through the doors...the intensity varies. Sometimes I smell it walking past a house or in a shopping area. Some materials absorb it...clothing, paper and so spread whatever it is to us all.
I made some videos earlier this year talking about it. I had a few people comment that they smell something too. One person said the vaxxed family member they live with smells so bad they have to sleep and mostly stay on the other side of the house. The best description given for what it smells like was "dryer sheets" but that's not where it's coming from.
https://www.bitchute.com/video/F20XHMixBUuA
I am a lay person trying to improve my understanding of the context of what's being discussed here. If "these plasmids in fact make spike RNA", does that happen by the promoters and/or enhancers reverse transcribing the code for the spike into the DNA of the cell, after which there is ongoing, ordinary expression of that code (involving RNA of course) and production of spike proteins? Or is there some other way in which the plasmids might make spike RNA? Thanks in advance.
Here is how it would happen in plain language. Vials are contaminated with residual DNA plasmids that contain the reverse transcribed mRNA that codes for the spike protein. The injected LNPs would therefore contain the mRNA for the spike protein but also contain DNA plasmids that have the reverse transcribed spike protein sequence in DNA form. When the LNP enters the cytoplasm of the cell, it breaks open and releases the mRNA and the DNA plasmid contaminant. The DNA that codes for the spike protein could, with promoters, become incorporated into the genome of that cell. When that cell transcribes mRNA from its DNA to make proteins, it could send out from its nucleus, mRNA that codes for the spike protein. So, we get persistent spike proteins that are coded for by the cell, not by the injected mRNA.
These scientists knew what they were doing . 🤬
or maybe not..., otherwise we'd have less dead victims.
Dead victims is the intention
That's what I thought was probably the case, but it's good to have it confirmed. Thanks very much.
From the Nepetalactone Newsletter:
"So this risk cannot be ruled out. Ultimately, one needs RNA-Seq data from these plasmids transfected in mammalian cells without the modRNA to see if these plasmids in fact make spike RNA. If they do, then that might explain persistent spike expression in patients. Once RNA is made, it already has the proper Kozak sequences to initiate translation in mammalian cells."
**********************
This seems to me to outline an approach to testing the hypothesis that contaminant plasmids in the mRNA "vaccines" may initiate "persistent spike expression in patients".
A persistent question for many of us is: "I'd like to know if unvaxed show signs of "spike" or whatever the new protein is actually. What if these rouge [rogue] plasmids spread somehow." (TheFrontPorchMedia, above)
(The pathology of PACS is of course an ongoing problem.)
Thanks, Jessica and Anandamide
I’m not sure if my question went through. Is it true that testing for the persistent spike proteins can only be done through research level testing? The everyday type of testing is not adequate?
The problem right now is that there is no way to reliably and affordably test for spike proteins in the blood directly. There is a lab in Germany that claims to be able to do it, http://Inmodia.de, but it is expensive. I had a recent discussion with Dr. Mark Trozzi MD, http://Dr.Trozzi.org, who is confident we will have a reliable method soon in the US and Canada. The testing we do now is measuring spike antibodies, an indirect way of estimating spike protein levels.
And as far as I know, testing for persistent spike proteins can only be accomplished through research level testing. Right?
"Vials are contaminated with residual DNA plasmids that contain the reverse transcribed mRNA that codes for the spike protein."
this does not sound logical, to me. A DNA plasmid should have DNA building blocks, not mRNA... Maybe what you mean here is the DNA plasmid encodes DNA sequence of the reverse transcribed Spike? If so, a reverse sequence would be incorporated with this gene 'therapy' into the human genome, not the one of the Spike.. Since the mod mRNA is recognized by the human ribosome, one can also suspect, a reverse transcription of that construct directly is also possible. That would give the 'normal Spike', not the reversed one.
The issues are always around the presence of the polymerases, one recognizing DNA and making its copy into mRNA, the other ('viral' one) reading RNA and making DNA out of it. And then we also have what SARS-CoV2 has, RdRp, RNA dependent RNA polymerase... The head is now spinning, in my case.
Truly speaking I'm kind of lost in the entire production 'procedure' but want to learn how it really works... Just sorry for the c-on-fusion.
And the guru of all, on this topic, David Baltimore, just died.., with 87.
“Maybe what you mean here is the DNA plasmid encodes DNA sequence of the reverse transcribed Spike?” Yes, that’s right. When the DNA sequence gets integrated, the nucleus can transcribe spike encoding mRNA from it. The spike encoding mRNA leaves the nucleus, and ribosomes will use that to make (translate) the spike protein.
Thanks Kevin (another one, just noticing;)), WAITED for that response AND the confirmation..
Also your other comment says:"The problem right now is that there is no way to reliably and affordably test for spike proteins in the blood directly. "
if so, how on earth every single blood test lists countless SINGLE proteins (albumin, globulin, etc., etc.) all related to many different diseases????
The biochemistry has all the tools they can to detect ANY protein, in particular such a lethal and toxic like Spike... Here one simple example:
https://systemx.stanford.edu/news/2023-01-20-000000/%E2%80%98theranos-works%E2%80%99-stanford-researchers-say-they%E2%80%99ve-measured-thousands titled "‘Theranos that works’: Stanford researchers say they’ve measured thousands of molecules from a single drop of blood"
So 'they' just DON'T DO it on PURPOSE, I do believe. Imagine scientists would detect ONLY the -PP- molecular clone of Spike in everyone. What would that mean??? We are all sick because of the injections only AND shedding of the toxic Spike from the injections only or the genetic material itself(equally from the injections only!!), with the latter I hope a LOT not being the case.
Oh, and there would be many ways to do that detection, btw. using exactly the same PCR test looking for JUST The specific, unique pieces of the Spike, like that region having the -PP- mutation I mentioned...
Optimizing Snyder’s setup to detect only spike protein is technically feasible and would reduce cost, labor, and analysis time. But even optimized, it is still far from inexpensive or simple enough for routine clinical or home testing. Currently, detection of vaccine-derived spike protein remains a high-sensitivity, specialized, and expensive lab task.
actually with your response, one more thought, about the possibility of incorporation of the reverse Spike sequence in nucleaus... A reverse Spike mRNA relative to the injected mod mRNA of Spike, after crossing the nucleus would mean a high probability of 'neutralisation'/silencing, or Spike fragments or the entire protein... Since many of the diseases come exactly from these fragments, anything what would initiate that silencing, would 'heal' the disease. Is that the big 'cure the cancer' advertisement?? Just a fantasy...
Sorry for any confusion on this topic. The reverse transcription is just a lab tool to replicate the mRNA, not to “reverse” the protein itself. If that reverse transcribed DNA got integrated into human DNA, the resulting mRNA would still make the same spike protein — it would not be reversed or ‘backwards’.
"Vials are contaminated with residual DNA plasmids that contain the reverse transcribed mRNA that codes for the spike protein."
If handwashing vials at lab sink doesn't work, maybe autoclahve should be utized to clean the vials. no?
Try as they may, there is no way to remove DNA contaminants from any shots called vaccines, including traditional childhood shots that do not use mRNA technology, or do not use DNA plasmids. DNA is always in there because of the media they grow it in. It could be animal DNA. It could be human DNA. I've been warning about this since 1984 when I first became aware of it.
"This is less clear that such an RNA would be translated in bacterial cells as it would require Shine-Dalgarno sequences in the RNA to attract bacterial ribosomes."
-> why do the injections knock out mainly one type of bacterial species, the bifidos?
The attention to the methylation sites tracking, reminds me of these news today:
"TruDiagnostic Wins $321K NIH Grant for Epigenetic-Based Disease Modeling Tech" with the quote:
"NEW YORK — TruDiagnostic said Tuesday that it has received a $320,511 grant from the National Institutes of Health to develop a system for disease modeling using epigenetic markers.
Called the W-Function Epigenomic Roadmap, the system will map DNA methylation changes to provide insights into disease onset, progression, and response to treatment, according to the Lexington, Kentucky-based company."
maybe unrelated..
So these cryptic promoters are like IRESes in mRNA?
There was some talk in the beginning about the mRNA having unknown IRES sites. At RiboClub Canada last year, there was a presentation about IRES sites in 3'UTR that could make 2 proteins from the same mRNA.
IRES are ribosomal translation start sites.
These are like IRES but for transcriptional start sites.
Thanks Kevin. Absolutely fascinating.
I don't know if my previous message went through. your pictures made me think of Barbara Newhall Follett. A brilliant precocious young woman, with a sensibility close to yours (I think).She led a charmed and strange life. I greatly respect you and what you do.
What if the vaccine payload was not the mRNA but in actual fact that was a ploy to get all that nasty DNA and stuff into the population.
Thank you, again.
We were all reassured that the carrying capacity of the LNPs was not much more than two modRNA transcripts, can one cram a full length pcDNA into an LNP ~90nm diameter?
maybe you should ask the author. this article was cross posted. also, if you do a simple search there's tons of info about extracting/isolating dna.