Also See: Explosive News: Irish Government (along with Canadian Government, see below) Can’t Prove ‘Covid’ Exists, Or That Social Distancing Or Mask Wearing Is Validated In Science – The Globalist Fascist Tyrannical Cult Narrative Pandemic/Virus Hoax Is Collapsing. https://wp.me/p19seq-aYo

The PCR Test Is Labelled NOT TO BE USED FOR ANY DIAGNOSTIC PURPOSES!! DR. TOM COWAN & KARY MULLIS [Test Inventor] This Is The Test That Fascist Governments Use To Establish The Presence Of Their Computer Generated Hoax Virus!

2) A weaponized spike protein toxic nanoparticle that’s being injected into people as a “clot shot” … and it’s likely shedding, causing harmful side effects in other, unvaccinated people.

3) A wholly fraudulent PCR “casedemic” scheme that’s designed to flag almost anyone as “positive” based almost entirely on how many cycles the PCR sample prep instruments are instructed to carry out, thereby amplifying instrument noise to the point of a “positive” hit. Almost anything can be flagged as “positive,” including genetic material fragments from previous years’ flu shots.

These three things — combined with the media’s mass hysteria programming — have achieved a level of global fear and psychological terrorism that the world has never seen before. But it’s all based on lies, it turns out. And here’s how we know.

No certified reference materials for isolated SARS-CoV-2 “covid-19” virus

As a lab owner, published scientist and mass spec analyst myself, I am extremely familiar with the process of using certified reference materials (CRMs) to validate analysis methods and instrument calibration sequences. (I’ve spent far too many evenings creating serial dilutions of standards using a Gilson pipette, trust me…)

Here’s how the process normally works in a legitimate science lab:

Step 1) Acquire the CRM of the thing you want to test (“analyte”). This means acquiring a purified, isolated standard with a known concentration, usually in a carrier such as water, or as a dry powder. For example, when I’m testing for mercury in food, I have a certified mercury standard with a known concentration of mercury, dissolved in water, nitric acid and hydrochloric acid.

Step 2) Run the CRM as a sample, at different concentrations, to build a “curve” that effectively teaches the instrument what the analyte looks like and how the instrument detector responds to different concentrations of the analyte. The end result is a “quant curve” that will be used in step 3.

NOTE: Instruments will “match” the thing you’re looking for by a variety of methods, filtering out all other things that don’t match. In mass spec work, molecules are identified by their molecular mass, ion fragmentation patterns, and elution time on chromatography columns. For a substance to match, it has to hit all these parameters. In PCR testing, a “match” is a genomic sequence made of base pairs, defined in a digital library that may or may not have ever been run against a real, physical standard in the real world.

Step 3) Run unknown samples through the instrument (of blood serum, urine, saliva, water, food sample extracts, etc.) and see if the unknown sample contains any of the thing you were looking for (the analyte). Because you built a quant curve, you can also then determine the concentration of the analyte in the original sample. This is typically described as mass over volume, such as ng / ml (nanograms per milliliter). A nanogram is a billionth of a gram. When we test foods for glyphosate, we can detect as little as 1 nanogram per milliliter, which tells you something about the extreme sensitivity of high-end instruments.

This is the process to test something and identify how much of something is found in something else. For example, if you were going to determine if someone was sick with “covid,” you would need to determine the concentration of covid-19 viruses in their blood (i.e. the “viral load”). This is science / biology 101.

So what’s the problem, then?

You’d be stunned to realize how deep the science fraud really goes. Consider these critical points:

Point #1: There appear to be no isolated, purified Certified Reference Materials available for SARS-CoV-2 “covid”.

I’ve seen companies that claim to be selling “isolates” containing covid viruses, but in their own description, they explain that their vials contain genetic material from “host cells” (human cells) as well as bovine serum cells, which means it’s a cocktail stew of who-knows-what. Yet it’s called an “isolate.”

Case in point: BEI Resources, which offers something they call an “isolate” of covid-19, that you can find at this link. As the description states for this covid-19 “isolate:”

…[T]his product is not suitable as a whole cell antigen preparation because the protein content is largely contributed by the host cell and the fetal bovine serum used during virus propagation.

In other words, most of the genetic material in the “isolate” is actually from human cells. So it’s not an isolate at all. The covid virus isn’t isolated. In fact, this “isolate” contains viral genetic material, human genetic material and bovine genetic material, plus whatever other viruses were present in the blood of the people and the cows. This could be millions of different nanoparticles present, each containing their own sequences of genetic material.

Point #2: If you have no isolated, certified reference materials, you can’t develop a legitimate analysis test. And this is exactly what the FDA admits in its own documents, which state that since covid-19 viruses weren’t available for the development of the PCR test, they “simulated” it by using human cells and gene bank coronavirus fragments. From the FDA’s own document:

Since no quantified virus isolates of the 2019-nCoV were available for CDC use at the time the test was developed and this study conducted, assays designed for detection of the 2019-nCoV RNA were tested with characterized stocks of in vitro transcribed full length RNA … spiked into a diluent consisting of a suspension of human A549 cells and viral transport medium (VTM) to mimic clinical specimen.

In other words, they faked the covid virus by using gene bank cells which were deliberately and falsely labeled “covid.” This is how the PCR test was developed. The FDA admits it all. The PCR test is a fraud.

Point #3: If you don’t have a CRM isolate, you can’t calibrate instruments against a known sample. And this means the PCR tests aren’t being calibrated against anything real and physical. Instead, they’re relying on downloaded digital libraries provided by none of than the CDC, the very same Big Pharma front group that’s spearheading this covid scam.

Point #4: PCR instruments are incapable of quantitative analysis. The “positive” hits are nothing but amplified background noise. No PCR instrument can tell you how much of some genetic material was found in an original sample. It can merely detect the presence of material on a yes / no basis. In lab science, this is called a “qualitative” analysis, not a quantitative analysis.

In qualitative analysis, the key factor is the “Limit of Detection” (LOD) of the instrument. How little of the sample will still create a “hit” for the instrument? In all instruments, for the LOD to be scientifically valid, it must be something that rises above background noise, or it’s scientifically meaningless. All instruments produce background noise, which are “peaks” or “hits” that represent detector static, you might say. These exist at a background level even when you’re running nothing in the instrument.

To show you what this looks like, consider the following graphic. It shows some mass spec results across a spectrum of masses. The horizontal axis here is m/z (mass over charge), which is simplified to just “mass” for general discussion. It’s the mass of the molecules or particles being detected.

Notice the red and orange lines across the bottom of each chart. That’s largely “background” noise across all the masses. Then notice the very tall orange peak which rises above the background. This is the mass of the molecule they’re looking for. It might be a pesticide, or a contaminant, or a nutrient, etc.

Importantly, if I were to turn up the amplification of the detector, the “background noise” at the bottom of the screen would vertically expand to fill the screen. The entire screen would be a “hit” on every mass, because the amplification is turned way up. That’s the equivalent to what PCR instruments are doing when they run 30+ cycles. They are amplifying noise, and then pretending they got a “hit” on covid.

But because they’ve amplified it so many times, they’ve obliterated any ability to say with certainty what they have, or even how much they have. Because the LOD (Limit of Detection) is scientifically invalid if it can’t pick a peak out of the background noise.

Typically in method validation, your LOD needs to be at least three times higher than background noise, which means a “peak” must be three times higher than the background. Anything less than that is considered bogus background noise. And when you’re doing quantitative work, you typically need a signal that’s at least 10 times higher than background.

Yet PCR instruments are taking background noise and amplifying it until they get a “positive” hit. This “positive” is then absurdly called a “covid case,” even though it means literally nothing from a legitimate science point of view.

The entire process being used today via PCR is complete junk science that wouldn’t pass even the most basic science lab audit. That’s why most of these PCR outfits aren’t ISO accredited, by the way. They couldn’t pass a single audit. (My lab is ISO accredited with an annual audit, including blind quantitation accuracy tests via mass spec instruments to make sure we are hitting our accuracy targets.)