Fantastic work Team mRNAReveal! In simple terms, would it be correct to interpret your findings that these vaccines contain spike (N1 MethylPseudoUridine) that unlike uracil/uridine found in C-19 infection, cannot be broken down by the body (as evidenced by Dr Mary Bowden's revelations about finding spike in injectees 3+ years after their last booster/shots)?
Now much more concerned about shedding given recent revelations by Pierre Kory et al as my MD partner is still brainwashed so getting shots regularly.
your findings continue to flood against the dam wall which is the FDA and HHS, who are conspicuously remaining silent when we can all reasonably assume they are peeking at this data from the shadows
this ongoing inertia of the FDA and HHS appears tied to this contamination possibly being the hottest political potato in Washington which currently persists in white washing away what we all know and can see - a global population impact event that is being allowed to continue
overnight former HHS advisor Dr Hatfill wentt on the record again with some of what is going on within HHS, the FDA, and the Trump administration .. worth the read for learning some of the BS politics being played to downplay the mushrooming data (yours) from currently seeing the light of day .. but here we are, on substack, seeing it all laid out for everyone
I can't make heads or tails of this, but it's absolutely fascinating, and justifies the intuitive sense of horror I felt four years ago when the vaccines were being mandated for us.
Because of the labors of Kevin and his colleagues, outside monitoring of Jab contents, (particularly from mRNA or related platforms) could become widespread and even routine.
This could 'fix' pharma better than any government regulator. 😎
Thanks, Jessica! I love receiving information from someone like you who really is a true professional microbiology researcher with massive knowledge, skill, intuition, equipment, and colleague support! The news is always filled with the junk science that amateurs and/or liars spew out in droves.
When you keep watching in a narrow way, you might not connect the dots. It is all there intentionally. It has a purpose. Furthermore, it is nefarious. They are psychopaths and sociopaths, who strive for more material wealth and power. They are after the children of Gaza, organs and blood, and when they are done they move on to the next country, and maybe your kids. Most idiots voted for them, some did not vote. Neither solved the problem, but are part of it. I solved the problem, and I give it to you for free. Cooperate broadly politically, but not with lying satanic psychopaths with ever-growing noses! Drop Team Trumpy Pumpkin, and drop Team Killary!
Does your ONT method also sequence RNA/DNA heteroduplexes? If not you might miss the bulk of the DNaseI protected DNA? I suspect RNA/DNA heteroduplexes are cytotoxic and genotixic but there is probably not a lot of research done on exogenous introduction.
We do RNaseA the sample before attempting to make an ONT library but I suspect alot of the DNA is single stranded as there is a molar excess of RNA to DNA so the DNA may need more time to anneal before we ligate the ONT adaptors to DNA with T4 DNA ligase. We also loose most of the small fragments through various SPRI steps and the spike is GC rich and may behave differently in sequencing than the insert. Buckhaults presented a coverage chart in his SC senate hearing that showed a big sequence difference between plasmid and insert sequence depth but he didnt use an RNase.
Probably most of the ssDNA is antisense so they have nothing to anneal to, correct? Do you heat up the sample while RNase A treatment? (because RNase A supposedly cannot degrade RNA in a heteroduplex)
I cleaned the kitchen but I also ate all of your food. :)
Hahaha. Jessica, love it!
Cleaning the kitchen caught my eye as well. One of the items on my Do List.....
OCD and famished...
;-)
always. need protein.
Last time I cleaned someone's kitchen out of goodwill, I also polished off the opened bottles in the drinks cupboard (to tidy it)
We're also going to publish this.
Hopefully it gets past the gate keeping. The research done here goes further than the previous paper?
Fantastic work Team mRNAReveal! In simple terms, would it be correct to interpret your findings that these vaccines contain spike (N1 MethylPseudoUridine) that unlike uracil/uridine found in C-19 infection, cannot be broken down by the body (as evidenced by Dr Mary Bowden's revelations about finding spike in injectees 3+ years after their last booster/shots)?
Now much more concerned about shedding given recent revelations by Pierre Kory et al as my MD partner is still brainwashed so getting shots regularly.
IMMENSELY THANKFUL to Dr. Rose and all of the others for using your BRILLIANT minds and expertise for the GOOD of humanity instead of for greed!
Fantastic, thank u . Now convince the other medical professionals who keep recommending the jab to patients.
thank you Kevin, Dr Rose, and Charles
your findings continue to flood against the dam wall which is the FDA and HHS, who are conspicuously remaining silent when we can all reasonably assume they are peeking at this data from the shadows
this ongoing inertia of the FDA and HHS appears tied to this contamination possibly being the hottest political potato in Washington which currently persists in white washing away what we all know and can see - a global population impact event that is being allowed to continue
overnight former HHS advisor Dr Hatfill wentt on the record again with some of what is going on within HHS, the FDA, and the Trump administration .. worth the read for learning some of the BS politics being played to downplay the mushrooming data (yours) from currently seeing the light of day .. but here we are, on substack, seeing it all laid out for everyone
https://drbowden.substack.com/p/the-quiet-subversion-and-capture
thank you again for keeping science on the proper keel
Julian Gillespie
I can't make heads or tails of this, but it's absolutely fascinating, and justifies the intuitive sense of horror I felt four years ago when the vaccines were being mandated for us.
Because of the labors of Kevin and his colleagues, outside monitoring of Jab contents, (particularly from mRNA or related platforms) could become widespread and even routine.
This could 'fix' pharma better than any government regulator. 😎
Damn good idea! 💪
Calling all grapevines 📞 ✍️ 📣 leading to RFK Junior & Joe Rogan!
Wowser
Thanks, Jessica! I love receiving information from someone like you who really is a true professional microbiology researcher with massive knowledge, skill, intuition, equipment, and colleague support! The news is always filled with the junk science that amateurs and/or liars spew out in droves.
Kevin, Jessica, and Charles, thank you for this necessary work.
Paws crossed that our "health regulators" will muster the courage to become interested.
So far . . . crickets!
Thank you to all! And, why do I keep finding you in my junk mail? I reset and, forward to my email, only then do I receive your Substack emails.🤷♀️
When you keep watching in a narrow way, you might not connect the dots. It is all there intentionally. It has a purpose. Furthermore, it is nefarious. They are psychopaths and sociopaths, who strive for more material wealth and power. They are after the children of Gaza, organs and blood, and when they are done they move on to the next country, and maybe your kids. Most idiots voted for them, some did not vote. Neither solved the problem, but are part of it. I solved the problem, and I give it to you for free. Cooperate broadly politically, but not with lying satanic psychopaths with ever-growing noses! Drop Team Trumpy Pumpkin, and drop Team Killary!
Does your ONT method also sequence RNA/DNA heteroduplexes? If not you might miss the bulk of the DNaseI protected DNA? I suspect RNA/DNA heteroduplexes are cytotoxic and genotixic but there is probably not a lot of research done on exogenous introduction.
We do RNaseA the sample before attempting to make an ONT library but I suspect alot of the DNA is single stranded as there is a molar excess of RNA to DNA so the DNA may need more time to anneal before we ligate the ONT adaptors to DNA with T4 DNA ligase. We also loose most of the small fragments through various SPRI steps and the spike is GC rich and may behave differently in sequencing than the insert. Buckhaults presented a coverage chart in his SC senate hearing that showed a big sequence difference between plasmid and insert sequence depth but he didnt use an RNase.
Probably most of the ssDNA is antisense so they have nothing to anneal to, correct? Do you heat up the sample while RNase A treatment? (because RNase A supposedly cannot degrade RNA in a heteroduplex)
We perform a 95C->4C step and then 500-1000X excess RNaseA at 37C