I have included more references to the thread that many people provided. Thank you. Fixed a few links and tried to clarify a few points people were confused over.
That was written at 1:00AM and I didn't find the Edit button until an hour ago:)
Someone forwarded me a lazy take down on Ivermectin (Not from a PCR expert).
S/He clearly read the Abstract of this small 24 person study which does mislead the average reader into thinking you can't obtain viral inhibition with human doses of IVM.
And while the study didn't find significant differences in the patients that were called positive (they nearly all were), it did see a shift in Viral loads on IVM (orange). Thats a log scale on Y.
So, why does the article tone this observation down? The abstract and conclusion bury this? Read it and decide for yourself but be certain to read the COI section.
Let's look at another slightly larger study in the same Journal.
In this case the authors have internal controls in their PCR.
And they understand p450 genetics enough to know that you shouldn't just measure the oral dose given, but instead measure the plasma level of the drug as some patients clear the drug quickly.
When these variables are controlled for you can see a reduction in viral load. This is a very important metric for the pandemic. If you want to dial down the scariant parade, you need to slow the polymerase or increase its fildelity. Vax programs that don't change viral load...
Invite more viral evolution.
But there is more. If you are a PCR geek that has any experience making reversible terminators you know that PCR signal is going to over estimate infectious viral load particularly when Ivermectin has many modes of action. So, one should confirm.
What is the impact of Ivermectin not just on qPCR signals of the viral RNA but on viability or culturability of the virus? Recall, Not all RNA is full length and when you stall polymerases, your qPCR signal and culture signal can diverge.
I can imagine if you start this study with late treatment, it will be too late to see the difference as once the virus has gone exponential, the drug may not be able to stop it. Apply it early and you are far more likely to see the the polymerae stall.
This review from Trevor Bedford confirms this.
Spike evolution is off the charts.
He is obfuscating the truth by calling it “partial immunity”.
Just say it!
Spike only Vax w/ same CT is Dumb.
Good to see him visualize a world without lockdown.
This charts lay out the Ks/Ka evaluation mentioned above.
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It is well known from BioNtech (Lenk et al) and Sutton et al (1997) that RNA:DNA hybrids inhibit DNaseI.
What is less known is that Quadruplex Gs also inhibit DNaseI. Some exist in SV40 and we get the most signal from this qPCR amplicon.
2 Different mechanisms of DNaseI inhibition = plasmid fragmentation cannot be assumed to be uniform in the mRNA vaccines. Hence 100 fold more spike than parts of the vector.
Below is a map of the codon optimized spike where Quadruplex Gs are overlaid with GAA repeats. GAA's are stickier RNA:DNA hybrids.
Our qPCR primers are overlayed as well.
@RetsefL @KUPERWASSERLAB @weldeiry @JesslovesMJK @DJSpeicher @TracyBethHoeg @DrJBhattacharya
Evans et al demonstrate DNaseI is resistant to quadruplex Gs. They also move to alternative enzymes. nature.com/articles/s4152…
This is from Lenk et al (BioNtech).
Note the concern over GAA sequences and RNA:DNA hybrids.
Our spike qPCR primers happen to land on GAA rich and quadruplex G rich regions of Spike. frontiersin.org/journals/molec…
@LocasaleLab I find the RNAi worship incongruent will how that entire field was ignored when injecting billions of people with mRNAs.
There are multiple 21bp homologies to human that emerged from the haphazard codon optimizations in the modRNA vaccine and no one cared?
@LocasaleLab Receipts.
Take Pfizers vax Sequence and run it through BLAT.
Hello... anyone from the RNAi space want to speak up about this?
On Veterans Day @CharlesRixey @JesslovesMJK
Stopped by MGC.
2 long days later we had all of his data.
It’s now published in The Journal of Independent Medicine.
It describes the mechanism of failure for the DNA contamination in the mRNA shots and why the regulators are missing it.
@JesslovesMJK @CharlesRixey @weldeiry @KUPERWASSERLAB @RetsefL @DrJBhattacharya @RWMaloneMD @RobertKennedyJr @TracyBethHoeg
Another Achs et al Fumble uncovered.
These folks don't even understand Capillary Electrophoresis.
Its becoming increasingly clear these are not honest mistakes but designed to deceive by people who are employed at a Vaccine Research Institute.
Science for Sale.
@JesslovesMJK @DJSpeicher
Here is the Rub.
They used a CE instrument that has a lower limit of sensitivity above the 10ng limit.
You need to be able to pick up 10X below the 10ng limit. Or 33pg/ul (300ul dose @ 10ng = 33pg/ul)
This is embarrassingly rigged or they are incompetent.
They ignored our comments on the preprint server and raced their paper into @Nature.
@JesslovesMJK and @DJSpeicher have their own substacks picking up other errors in this paper I'll post sortly.