I would argue that the clotting found in Covid infections and vaccine injuries been caused by the spike protein rather than graphene oxide is actually Occam's razor here, and I am relatively sure at least 95% of people would agree with that assessment.
I would argue that the clotting found in Covid infections and vaccine injuries been caused by the spike protein rather than graphene oxide is actually Occam's razor here, and I am relatively sure at least 95% of people would agree with that assessment.
My problem with the spike protein narrative is that, as far as I understand, the hydrogel-embedded mRNA starts up a chain reaction that cannot be controlled.
The number of people echoing the same thing doesn't make it true...
Hydrogels are supposedly degraded by EDTA, the strongest metal chelator out there. To destroy the toxic synthetic genetic material should be known too, at least by those criminals who produce it.... Even the synthetics needs to be 'protected' by the lipids and nanos, thus something should be able to get rid of it, enzymes which can cut it down. Well, once you have the wrong building blocks I don't know how the body gets rid of that 1-methy-pseudouridine....
my entire substack is all about the mRNA sequences and connections via the pathways they encode.. It is the DIRECT PROOF of the genocide, alone by studying that genetic sequence. Hope you can learn something from my posts..
yes, that's the nice thing, but there is one condition for everyone on an open platform, we shall not lie, knowingly or unknowingly. That's why my comment about the RIP Andreas...
Andreas was authentic; he gave his life for the truth.
Here, I can see an opportunity for you and I to have a nice and productive discussion, possibly in private first, because I am sensing that a lot of discrepancies will have to be straightened out.
Once you read all my posts you will learn some of my points of view. Definitely truth tellers will overlap in their message and that has to become official, a.s.a.p. before even more HUMANS get killed on this planet. Btw. I'm authentic, like Andreas, just still alive, luckily.
You and I are both committed to searching for the truth and every piece of incoming information must be accommodated... Sometimes it takes a long time to do that...
We are operating airplanes in fog without GPS...
The only tools we have is triangulating and factoring.
The good news is that everything seems to be pointing in one direction, so a lot of errors/lies can be eliminated without being "experts." :)
As a communication and linguistic specialist, you probably do not operate an airplain, ha? And that on top of a space-time structure in which there is no dot without GPS...
one could find that out, maybe even done already.. Get the commercial Spike powder and rGO. Concentrate both to appropriate level in physiological solutions and mix up with blood under microscope while filming what is happening. The difference between what is happening while having the jabs is, that the Spike or its parts (S1 or S2 ) is actually embedded in the cell membranes which bind ACE2, which is in all blood vessels and on surface of many organs.... The pathological findings from Prof. BRurkhardt showed that the SPike is also freely floating in cells, thus that suggested experiment would give the proper answer at least in part. Reduced Grahene Oxide (rGP) is a FLAT, electrically and thermally conductive surface capable to cut proteins/DNA via the edges, get into brain directly^1, etc. but it would be hard to imagine it is capable of stacking the entire red blood cells regularly or clumping them entirely, like what is known to be done by wi-fi radiation, interacting with iron dipole moments of the hemoglobin molecules. While cutting comepletely randomly in blood rGO would create a mass of byproducts seen as a big clump, but not as a regular organized entity.
I'm looking for papers on the graphene influenced blood stacking, so far nothing out there. Thus the suggested experiment could be useful.
1. PEGylation of reduced graphene oxide induces toxicity in cells of the blood-brain barrier: an in vitro and in vivo study. 06 Oct 2016 Molecular Pharmaceutics.
I just want to note that even though we have a little bit of a disagreement over the vaccine terminology, I sincerely appreciate the work you do and the analyses you put together. How do you spoke with the best person I know today and they thought most likely these issues would be explained by the spike proteins homology with factor XII, so what we are going to do over the next week and see if the correct region of factor XII is mimicked on the spike proteins, what occurs in the simulated docking experiments and how this region of the spike protein compares to the original SARS virus which did not cause clotting under any circumstances.
Also, Wi-Fi and other forms of microwave radiation does interfere with zeta potential.
"PEGylation of reduced graphene oxide induces toxicity in cells of the blood-brain barrier: an in vitro and in vivo study" actually puts a little table with your potentials, here a cut and paste for you:
Table 2. Physicochemical characteristics of non-PEGylated and PEGylated rGO.
"A comparison of zeta potential revealed that the charge associated with the non-
PEG rGO had a greater negative zeta potential (тИТ25 ┬▒ 0.18 mV) than the PEGylated rGO (-4.2 ┬▒ 3.8 mV). This suggests the existence of positive amino-ended branches, resulting in a lesser negative electrostatic charge for PEGylated rGO than rGO (Vila et al. 2012). The PEGylation of rGO leads to a decrease in PDI values (0.56 ┬▒ 0.03 to 0.39 ┬▒ 0.04), resulting in the diminished polydispersity of particles, probably due to a lower susceptibility to aggregate formation.
A significant increase in size, from 342 ┬▒ 23.5 nm up to 910 ┬▒ 32.7 nm, was
found after PEGylation. Although this increase offers evidence for the PEGylation of
nanoparticles, confirmation of the attachment of PEG to rGO is essential."
The PEG2000 in the shots is rather large, but still 3x smaller than the size used in this paper, thus these rGO+PEG clusters would be smaller in comparison to these sizes mentioned here.
Thank you for this. When I read through the lease expires or EMA papers, I was able to find some information on the zeta potential of the lipid nano particles, but I was never subsequently able to find anything on the zeta potential of the spike protein, the Covid virus, or graphene oxide. With the spike protein, we instead did the next best thing which was to compare the density of positive charge groups, is that normally lines up with how something will affect Zeta potential. Overall, for the lipid nano particles to do their job, they could not have a negative charge because that would've prevented them from being able to enter negatively charge cells, but the same time they also needed to remain dispersed from each other so they did not agglomerate together once injected.
If you wanna come across any more papers that specific roles of anything related to these things, please send them my way.
just started to learn little bit about colloidal solutions. The zeta potential has no meaning if you do not know the pH, ion concentration surrounding the colloids. The nanos in the injection materials are known to behave differently at different pH values. Supposedly they are neutral in the vials but aquire strong positive charge when entering the body at the physiological pH, thus literally bombarding, punching holes and going through the negatively charged cells walls.
these are STATIC quantities, always connected to the 3D geometry of charge distribution inside of the entire object. It moves with it or changes when the shape is changing. For that post I calculated the Spike dipole moment and showed there that it is exactly directed toward the 3-meric axis of the complex which enters the cell membrane. It is like a needle punching the hole in the already hugely charged lipid bilayers of every normal cell.
The charges inside of the Spike are the key, in my opinion.
that is really interesting. I wonder if something that suited to the task could have formed naturally...
I also wonder how having focused linear areas of high charge densities affects zeta potential because in the past I've always looked at the cation being symetrical/spherical in its effect.
I would argue that the clotting found in Covid infections and vaccine injuries been caused by the spike protein rather than graphene oxide is actually Occam's razor here, and I am relatively sure at least 95% of people would agree with that assessment.
Thank you for your reply.
My problem with the spike protein narrative is that, as far as I understand, the hydrogel-embedded mRNA starts up a chain reaction that cannot be controlled.
The number of people echoing the same thing doesn't make it true...
Hydrogels are supposedly degraded by EDTA, the strongest metal chelator out there. To destroy the toxic synthetic genetic material should be known too, at least by those criminals who produce it.... Even the synthetics needs to be 'protected' by the lipids and nanos, thus something should be able to get rid of it, enzymes which can cut it down. Well, once you have the wrong building blocks I don't know how the body gets rid of that 1-methy-pseudouridine....
Hydrogels tend to be deadly, too, but not as bad as the mRNA stuff, which is, according to Dr. Andreas Noack, it a red herring:
https://rayhorvaththesource.substack.com/p/mrna
my entire substack is all about the mRNA sequences and connections via the pathways they encode.. It is the DIRECT PROOF of the genocide, alone by studying that genetic sequence. Hope you can learn something from my posts..
As every batch is different, the manufacturers can always claim "contamination" or "rare side effects" regarding the deaths and the injuries.
I also hope, I can learn something from your posts. :) After all, learning from others is one of my primary objectives!
https://rayhorvaththesource.substack.com/p/activators?utm_source=%2Fprofile%2F42034032-ray-horvath-the-source-&utm_medium=reader2
The best thing about it is that you and I don't have to agree! We are both responsible for our own decisions!
yes, that's the nice thing, but there is one condition for everyone on an open platform, we shall not lie, knowingly or unknowingly. That's why my comment about the RIP Andreas...
Andreas was authentic; he gave his life for the truth.
Here, I can see an opportunity for you and I to have a nice and productive discussion, possibly in private first, because I am sensing that a lot of discrepancies will have to be straightened out.
Are you interested?
Once you read all my posts you will learn some of my points of view. Definitely truth tellers will overlap in their message and that has to become official, a.s.a.p. before even more HUMANS get killed on this planet. Btw. I'm authentic, like Andreas, just still alive, luckily.
Welcome to the club! :)
Being afraid is not going to save anyone.
Still, it doesn't look like authentic people will last much longer. The delivery systems for the poisons are now, apparently, untraceable...
You and I are both committed to searching for the truth and every piece of incoming information must be accommodated... Sometimes it takes a long time to do that...
We are operating airplanes in fog without GPS...
The only tools we have is triangulating and factoring.
The good news is that everything seems to be pointing in one direction, so a lot of errors/lies can be eliminated without being "experts." :)
As a communication and linguistic specialist, you probably do not operate an airplain, ha? And that on top of a space-time structure in which there is no dot without GPS...
I can operate a lot of things. :) That is irrelevant. The question is, how far does it take me! :D
one could find that out, maybe even done already.. Get the commercial Spike powder and rGO. Concentrate both to appropriate level in physiological solutions and mix up with blood under microscope while filming what is happening. The difference between what is happening while having the jabs is, that the Spike or its parts (S1 or S2 ) is actually embedded in the cell membranes which bind ACE2, which is in all blood vessels and on surface of many organs.... The pathological findings from Prof. BRurkhardt showed that the SPike is also freely floating in cells, thus that suggested experiment would give the proper answer at least in part. Reduced Grahene Oxide (rGP) is a FLAT, electrically and thermally conductive surface capable to cut proteins/DNA via the edges, get into brain directly^1, etc. but it would be hard to imagine it is capable of stacking the entire red blood cells regularly or clumping them entirely, like what is known to be done by wi-fi radiation, interacting with iron dipole moments of the hemoglobin molecules. While cutting comepletely randomly in blood rGO would create a mass of byproducts seen as a big clump, but not as a regular organized entity.
I'm looking for papers on the graphene influenced blood stacking, so far nothing out there. Thus the suggested experiment could be useful.
1. PEGylation of reduced graphene oxide induces toxicity in cells of the blood-brain barrier: an in vitro and in vivo study. 06 Oct 2016 Molecular Pharmaceutics.
I just want to note that even though we have a little bit of a disagreement over the vaccine terminology, I sincerely appreciate the work you do and the analyses you put together. How do you spoke with the best person I know today and they thought most likely these issues would be explained by the spike proteins homology with factor XII, so what we are going to do over the next week and see if the correct region of factor XII is mimicked on the spike proteins, what occurs in the simulated docking experiments and how this region of the spike protein compares to the original SARS virus which did not cause clotting under any circumstances.
Also, Wi-Fi and other forms of microwave radiation does interfere with zeta potential.
Thank you. That paper I just mentioned:
"PEGylation of reduced graphene oxide induces toxicity in cells of the blood-brain barrier: an in vitro and in vivo study" actually puts a little table with your potentials, here a cut and paste for you:
Table 2. Physicochemical characteristics of non-PEGylated and PEGylated rGO.
Samples Size (nm) Zeta potential (mV) PDI
Non-PEGylated rGO 342 ┬▒ 23.5 тИТ25 ┬▒ 0.18 0.56 ┬▒ 0.03
PEGylated rGO 910 ┬▒ 32.7 -4.2 ┬▒ 3.8 0.39 ┬▒ 0.04
and a quote, in case you can't get this paper:
"A comparison of zeta potential revealed that the charge associated with the non-
PEG rGO had a greater negative zeta potential (тИТ25 ┬▒ 0.18 mV) than the PEGylated rGO (-4.2 ┬▒ 3.8 mV). This suggests the existence of positive amino-ended branches, resulting in a lesser negative electrostatic charge for PEGylated rGO than rGO (Vila et al. 2012). The PEGylation of rGO leads to a decrease in PDI values (0.56 ┬▒ 0.03 to 0.39 ┬▒ 0.04), resulting in the diminished polydispersity of particles, probably due to a lower susceptibility to aggregate formation.
A significant increase in size, from 342 ┬▒ 23.5 nm up to 910 ┬▒ 32.7 nm, was
found after PEGylation. Although this increase offers evidence for the PEGylation of
nanoparticles, confirmation of the attachment of PEG to rGO is essential."
The PEG2000 in the shots is rather large, but still 3x smaller than the size used in this paper, thus these rGO+PEG clusters would be smaller in comparison to these sizes mentioned here.
Thank you for this. When I read through the lease expires or EMA papers, I was able to find some information on the zeta potential of the lipid nano particles, but I was never subsequently able to find anything on the zeta potential of the spike protein, the Covid virus, or graphene oxide. With the spike protein, we instead did the next best thing which was to compare the density of positive charge groups, is that normally lines up with how something will affect Zeta potential. Overall, for the lipid nano particles to do their job, they could not have a negative charge because that would've prevented them from being able to enter negatively charge cells, but the same time they also needed to remain dispersed from each other so they did not agglomerate together once injected.
If you wanna come across any more papers that specific roles of anything related to these things, please send them my way.
just started to learn little bit about colloidal solutions. The zeta potential has no meaning if you do not know the pH, ion concentration surrounding the colloids. The nanos in the injection materials are known to behave differently at different pH values. Supposedly they are neutral in the vials but aquire strong positive charge when entering the body at the physiological pH, thus literally bombarding, punching holes and going through the negatively charged cells walls.
Yup it's a very complicated subject.
yes, it is. I look lot into dipole moments of macromolecules and gave a small intro in:
https://mejbcart.substack.com/p/sars-cov-2-spike-protein-5g-and-covid19
these are STATIC quantities, always connected to the 3D geometry of charge distribution inside of the entire object. It moves with it or changes when the shape is changing. For that post I calculated the Spike dipole moment and showed there that it is exactly directed toward the 3-meric axis of the complex which enters the cell membrane. It is like a needle punching the hole in the already hugely charged lipid bilayers of every normal cell.
The charges inside of the Spike are the key, in my opinion.
that is really interesting. I wonder if something that suited to the task could have formed naturally...
I also wonder how having focused linear areas of high charge densities affects zeta potential because in the past I've always looked at the cation being symetrical/spherical in its effect.
Out of curiosity, what is your background?
This is strange, substack erased all my personal info... Under my newsletter there was always that info, but no more now., just wonder why??:
Anyway my fields are, or better, were..:
physics/biophysics, macromolecular crystallography with bioinformatics, synchrotron instumentation...
In regard to ionic shapes, look at the molecular orbitals, there are rarely spherical..