In a shocking revelation first reported by Dan Dicks of Press for Truth(Canada), an FDA document admits that the CDC and FDA conspired to fabricate a covid-19 testing protocol using human cells combined with common cold virus fragments because available.
Sinceand this study conducted, assays designed for detection of the 2019-nCoV RNA were tested with characterized stocks of in vitro transcribed full length RNA (N gene; GenBank accession: MN908947.2) of known titer (RNA copies/µL) spiked into a diluent consisting of a suspension of human A549 cells andviral transport medium (VTM) to mimic clinical specimen.
In other words, they had no covid virus from which to develop and calibrate the test, so they mixed up a cocktail of human cells and RNA fragments from a common cold virus, then called it “covid.” The GenBank sequence referred to in this paragraph is simply but has no supporting reference materials in physical reality either.
That’s because . As a result, no laboratory instruments can be calibrated against actual covid, and the tests simply rely on digital libraries pushed out by the CDC and WHO, using “covid” as the label.
The PCR tests are then instructed to look for these genetic sequences obtained from the fabricated digital libraries, meaning the entire scheme is junk science circular logic with no basis in physical reality.
To be clear, I’m not saying that viruses don’t exist, and it’s quite clear that the Wuhan Institute of Virology colluded with Fauci, Daszak, the NIH, Baric and others to develop a weaponized spike protein. But . It’s simply a toxic nanoparticle that can be synthesized in quantity and then either dumped on cities or added to vaccines and injected into people via immunization protocols.
ask the big question about all this in my science lab whistleblower video here, which presents more details about all this that will have your head spinning. In essence, And why were no such materials used in the development of the FDA-approved, CDC-endorsed PCR testing protocols?