The U.S. Army just announced their new creation of a Spike Ferritin Nanoparticle (SpFN) “vaccine”, claiming that it works “against all existing COVID & SARS variants”. Without animal testing or safety studies, Human trials are already underway.
The U.S. Army published a series of preclinical studies claiming the Spike Ferritin Nanoparticle serum “protects against heterologous challenge with B.1.1.7 and B.1.351 virus variants” during an animal trial. This is key to understanding what they’re really doing with these death jabs.
“B.1.1.7” and “B.1.351” are literal genetic lineages that contain your God-given genetic information. Heterologous challenges result from cross-species genomics. When you delete genes and code Human cells with insect DNA (Luciferase) and monkey DNA, bad things happen. It’s called genetic mutation.
The official narrative explains that the B.1.1.7 Alpha variant of SARS-CoV-2, the supposed “virus” that causes COVID-19, has turned up in the UK and the B.1.351 Beta variant in South Africa. Then there’s the B.1.1.529 Omicron variant which is new on the scene. Now I’m going to explain to you how you’re being fooled because first they fool you then they rule you.
The CDC website mentions the “variant of concern (VOC), lineage B.1.1.7 is also referred to as VOC 202012/01 or 20I/501Y.V1”. Another page of the CDC website says about the B.1.1.7 variant, “This variant has a mutation in the receptor binding domain (RBD) of the spike protein at position 501, where the amino acid asparagine (N) has been replacedwith tyrosine (Y). The shorthand for this mutation is N501Y”.
The key word in that quotation is REPLACED.
TheBullfrog
Look up N501Y and you find that it’s a genetic mutation resulting from reverse genetics (cloning). Reverse genetics involves directed gene deletions and point mutations (site-directed mutagenesis) to create null alleles (non-functional); which is gene knockouts. These gene deletions lead to permanent loss-of-function.
CRISPR-Cas9 – technology is raping your cells’ genome and cutting it at a specific location to allow genes to be removed and new engineered sequences to be inserted using RNA interferenceto permanently silence genes. Genetic knockdowns are typically temporary whereas genetic knockouts are permanent.
Moderna and other pharmaceutical bioterrorists researched extensively the knockout of genes in regards to “curing cancer” and what the reduction of amino acid asparagine (N) causes. The CDC says the amino acid asparagine (N) has been replaced with tyrosine (Y). When you knockout genes, the protein associated with that gene stops being produced by your cells. In this case it’s the amino acid asparagine (N) that has been replaced with tyrosine (Y) which causes rapid cancer growth. They want you sick and dying.
The N501Ymutationis being induced by gene deletion, to cross the species barrier so that animal diseases (monkey disease) can create infection in Human cells that would not naturally occur. Since animal diseases do not infect Humans, cloning is necessary.
The UK Government says the “VOC-202012/01 variant includes 23 changes in the “virus” with eight mutations (changes) in the outer “spike” protein; nine changes that alter the amino acid sequence of proteins elsewhere in the virus genome, and six changes that do not alter the amino acid sequence of proteins elsewhere in the virus genome”.
What they are really talking about is YOU. Since viruses are still a theory and have never been proven to exist, governments and the pharmaceutical cartel are using the word “virus” to deceive the medical community and divert our attention away from their Bioterrorism. They want us to believe that a boogey virus mysteriously jumped from bats to Humans when actually they’re making changes to the Human genome.
This study confirms that SARS-CoV is nothing but “S glycoproteins” made using an unnatural genetic sequences that fools your cells into thinking it’s natural so your body will not reject the biohacking technology.
The Spike Ferritin Nanoparticle SpFN WO2021178971A1 patent, also confirms that the SARS-CoV is an “glycoprotein S” which is the “spike protein”.
So there you go, mystery solved. The infamous “spike protein” is not a “spike” protein from a “virus” after all. The glycoprotein S is a chimeric Bioweapon.
The SpFN patent also contains the transfection agent HEK293T/17 which is Human embryonic kidney DNA. It’s a chimeric “pcDNA” for cloning.
Thermo Fischer is using a “pcDNA cloning kit” which also does gene deletion.
The SpFN patent also contains HIV-1 which is patented and owned by the treasonous, mass murdering, Genocidal Anthony Fauci. It also has Luciferase (insect DNA) for tracking your every move. Oh yeah… and the patent confirms it came from Wuhan, China!
Aluminum Hydroxide is also listed in the SpFN patent and Aluminum Hydroxideis made from Graphene Oxide. They call it “Alhydrogel”. So… Graphene Oxide is irrefutably in the SpFN Bioweapon shots!
It gets even more disgusting. They’re using bullfrog DNA to create their chimeric glycoprotein “S”.
Who wouldn’t want to be transfected and cloned with bullfrog? Because if you don’t accept their Franken-vaxx, then you’re a racist… against the bullfrog species!
GENE DELETION
Studies show that the B.1.1.7 “variant” is directly caused by gene 69-70 deletion in Humans. The B.1.351 “variant” is directly caused by gene241–243 deletion.
The CDC openly admits that the Omicron variant is the result of an “S gene drop out” caused by “gene 69-70 deletion”.
The World Health Organization says that the S gene is not present in the Omicron variant. In its report titled “Classification of Omicron (B.1.1.529): SARS-CoV-2 Variant of Concern“, the WHO’s Technical Advisory Group on SARS-CoV-2 Virus Evolution (TAG-VE) confirmed that the RT-PCR kits which are designed to target the S gene, detect a complete dropout of the S gene.
Thermo Fisher’s Genetic Sciences Division revealed that the B.1.1.7 variant is the result of gene mutation caused by the gene deletion of the “S gene”. Thermo Fisher explains that the “S gene” is a 69-70 deletion. Thermo Fisher admits that gene deletion mutations is the cause of all SARS-CoV-2 variants, Lambda, Alpha, Beta, Gamma, Delta, etc.
Are you catching on? The “S” gene is the glycoprotein S Bioweapon, an artificial genetic sequence that’s being coded into Human cells (transfection/cloning) after gene knockout.
“The Omicron variant has been found to include the 69-70del mutation of the S gene, first identified as a mutation in the Alpha variant. This mutation causes a dropout of the S-gene target in results from widely used TaqPath COVID-19 Detection Kits. An S-gene failure does not mean a result is negative, only that the S gene was not detected. Multiple public health organizations have noted that this pattern of detection (i.e. S-gene dropout) can be used as a marker for this variant, pending sequencing confirmation.”
So there you have it. The PCR kits target genes for gene deletions and monitor the cloning progress.
All Covid vaxx patents mention gene deletion. Both Pfizer and Moderna claim their serums “protect against” the variants. The Moderna patent states it’s death jab is “folding proteins”. The folding of proteins induces genetic mutations.
The Pfizer patent directly states that it’s serum is deleting genes 69-70 and 242-244. So these lying bastards are not “protecting” against anything. They are inducing the scary variants through gene deletion.
Do not drink their poison.
The Pfizer vaxx patent also mentions the N501Y mutation due to but not limited to 69-70 gene deletions. Remember, 144 gene deletion causes rapid cancer growth.
Pfizer patentWO2021213945A1
Thermo Fisher owns the patent to a PCR kit that “targets genes”. The PCR kit is also a marker to “test” for gene deletions to determine if the jabbed are patent eligible.
Thermo Fisher sells the Microbeads used in the death jabs and markets them as Dynabeads and SPIONs. Then they have a PCR kit to “test” how their cloning project is going.
Cloning any species results in mutations that are unpredictable, as I previously documented in my articles here, here and here.
CONCLUSION
Variants are caused by gene deletion from fake vaccines and fake tests. Stop complying to your Democide and Mark of The Beast enslavement.
Serve the war criminals (anyone pushing the death jab) with Notices of Liability.
Contact me or book a free consultation and I will help you design a detox protocol that fits your needs and your budget, to remove the biological poisons we are being bombarded with. Do not loose hope because there are solutions to save and protect your health.
Dark Field Microscopy image of Graphene Hydroxide nano-razorblades
In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased.
Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide.
You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here.
LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY
Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair.
Microbubbles and Microspheres (bottom right)
Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells.
Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this.
Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.”
Crystalline scaffoldingfrom the #DeathJab
This technology is being used for DNA-based tissue engineering and “scaffolding” of Humans, without their Informed Consent. See more scaffolding images from a Slovakian study of the death jab, here.
Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside.
This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids.
The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies.
Moderna patent US10703789B2delayed drug release
QUANTOM DOTS& MICROBEADS
Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents.
These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene.
Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans.They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans.
Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move.
I discussed Quantum Dots and more with Stew Peters on December 9th, 2021.
Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021
Microbeadpatent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and MicrobeadpatentES2784361T3/en specifies that it’s used to create molecular barcodes in Humans.
This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dotpatent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide.
Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys.
Moderna’s patents are owned by Israel. Pfizer patents are owned by Israel. Pfizer CEO is in bed with Israel. Moderna is partnered with Israelin medical maleficence.
Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS!
Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect.Is that what you want to become?
BIOCHIP& HYDROGEL
Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”.
Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal.
We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc.
Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol.
PROTOCOL
There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here.
The transhumanist dystopian nightmare we find ourselves in is taking a new turn with the shocking discovery of Hydra Vulgaris and PARASITES in the so-called Covid-19 “vaccines”.
Dr. Carrie Madej revealed her Hydra findings on the Stew Peter’s Show on September 29th, 2021, followed by Dr. Zandre Botha’s stunning discovery of microscopic, self-assembling medical devices in the blood of her vaxxed patients. The red blood cells are dangerously deformed and coagulated, things she says she’s never seen before in her 15 years as a blood doctor.
Hydra Vulgaris identified in Pfizer & Moderna Covid-19 serums
About 10 days later, “That Thing” (Hydra Vulgaris) was also identified in Pfizer vials by Dr. Franc Zalewski. He took the science to a new level and did a chemical analysis of the Hydra, exposing that the chemical compound of the creature contains Aluminum, Carbon, and Bromium. This means the Hydra’s are being genetically modified before they’re injected into humans. The good doctor also identified parasites in the vials.
Dr. Jane Ruby, a pharmaceutical researcher, gave vital commentary on Stew Peter’s Show about Dr. Zalewski’s findings, emphasizing that the dormant Hydra “eggs” become active, grow and multiply when exposed to Graphite tape and heat.
Earlier in August, parasites and other horrors were identified by Dr. Robert Young in four Covid-19 vials. Dr. Jane Ruby again joined Stew Peters to give crucial commentary on Dr. Young’s findings.
Investigative Journalist Ramola D. provided us with further information about the parasites discovered by Dr. Young and did an expose in October.
Back in July, La Quinta Columna studied four “vaccines”; Pfizer, Moderna, AstraZeneca, and Johnson & Johnson, and found toxic nano metallic particulates, particularly nanographene oxide, in significant amounts, as well as lipid nanoparticles and the parasite Trypanosoma cruzii, in the Pfizer-BioNTech serum.
Pfizer whistleblower Karen Kingston appeared on Stew Peter’s Show in July and walked us through a presentation on how Graphene Oxide is in all Covid-19 serums. Graphene Oxide was not listed in the patent filings and was deliberately concealed under a trade secrete because it’s known to be poisonous to humans.
As a result of these horrifying discoveries, I did my own research on Graphene Oxide Nanoparticles and Toxicity and wrote an article entitled “Graphene Oxide The Vector For Covid-19 Democide“. I reveal how humanity is being saturated with Graphene Oxide Nanoparticles in a myriad of ways.
I also wrote an article on protocols for detoxifying Graphene Oxide from your body, here.
The openly declared ingredients in Covid-19 serums should be enough to dissuade anybody from taking them. Now it’s clear there are additional poisonous and other horrors not being disclosed to the public by the Biotech pharma industry.
Karen Kingston has backed up all these terrifying discoveries with the patent filings and receipts, on Stew Peter’s Show. Kingston explains that the vaxxines are a “gateway to an obedience platform and potentially an execution platform if you are not obedient to your score”.
Informed Consent has been waived and therefore people didn’t know they’re being injected with smart devices and bioweapons. The patents also reveal that it was alreadyknown by Pfizer that the vaxxed would become “super spreaders” and transmit deadly pathogens to healthy individuals.
There’s an AI component to these vaxxines Kingston explains, “they’re committed to replacing the American people with Artificial Intelligence”. She continues disclosing that “Hong Kong is ready to replace the American people with robots right now”.
Due to the fact that patent filings do not reveal the components to Biotech’s vaxxine ingredients, I began researching scientific peer-reviewed studies involving Hydra Vulgaris and parasites to see if I could identify why they’re being injected into humans.
GAIN-OF-FUNCTION
Everything I’m writing here is based on evidence from open-source, peer-reviewed literature of scientific breakthroughs and technological developments that extend through the past decades and are linked in this article. As sci-fi thrilling as this information may sound, the technology has already been deployed and is being injected into the veins of our children as we speak. You can read the studies for yourself, as I have done.
DNA hybridization began in 1980 with Nadrian C. Seeman who started constructing self-assembled nanostructures. Hydra Vulgaris transgenesis technology was developed over the last 30 years. This is the process of transferring genes and organisms from one species to another which creates a new cloned species.
The Human Genome Project began in the year 2,000. Hydra’s are used in the human genome assembly for gene silencing of humans. Messenger RNA (mRNA), SPIONS (Super Paramagnetic Iron Oxide Nanoparticles), DNA coated lipid-nanoparticles containing drugs and chemicals, transgenic Hydra’s and parasites are all part of an “operating system” which is bypassing the human immune system. You can read more about Moderna’s “operating system”from their own website,here.
Graphene Oxide sheets are used to slice open the membrane of your cells so that programmable Nanorobots can reach the cell nuclei to turn off undesired genes (gene silencing) and code artificial gene sequences. This process is called biohacking.
Graphene Oxide sheets are able to slice open every cell membrane of the human body within 15 minutes after inoculation, according to Dr. Robert Martin.
The Sixth International Workshop on DNA Nanotechnology was held August 26–28, in 2017, in Beijing, China where the forum showcased the applications of self-assembled DNA nanostructures.
CHIMERIC SPIKE PROTEIN
The “spike protein” in the Covid-19 vaxxines that everyone is talking about is called a Lentivirus. The Lentivirus contains a combination of HIV types 1-3, SRV-1/AIDS, MERS,andSARS. These are the most deadly Gain-Of-Function bioweapons ever developed, thanks to mass-murdering Fauci.
A Stanford study reveals that the Lentivirus is a “genus of retroviruses that cause chronic and deadly diseases characterized by long incubation periods, in humans”. It enables long-term transgene expression. The best-known Lentivirus is the human immunodeficiency pathogen, which causes AIDS. This is why we’re seeing an autoimmune and neurodegenerative decline after Covid-19 inoculation. This is an induced condition known as PRION.
The mRNA from the Lentivirus chimeric cocktail is inserted into the DNA of human cells through an invasive procedure that permanently changes the genome of that cell. Once inside the host cell’s cytoplasm, lipid-coated nanobots take the reverse transcriptase enzyme in the Lentivirus to produce DNA from the mRNA genome, the reverse of the usual pattern, thus retro.
Morphogenesis and stem-cell control using the Hydras were developed to learn the neurobiological functions of humans and for in vivo tracing of cells. Transgenic Hydraallows in vivotracking of individual stem cells during morphogenesis (tissue and cell growth).
Transgenic Hydra lines are generated by embryo microinjection with plasmid DNA from self-replicating DNA found in bacteria. This is a permanent transmissible change of genetic material (DNA) resulting in the decreased production of a protein. The merging of the two species is a“cloning”processcalled transfection. A new generation of transgenic Hydra polyps continues reproducing the chimeric genetic expression in their offspring.
These GMO Hydra polyps are now genetically codedvectors, carrying a variety of programmed synthetic genomic sequences and mRNA (messenger RNA) for the purpose of transfecting humans. Once inside the human body, these transgenic Hydra polyps serve to rewire and control the ancestral circuitry of human beings.
BLAST Sequence technology is being used to create new DNA sequences and find similar genetic sequences between species, performing alignment functions for same-species and cross-species genetic splicing for the purpose of transcription.
Proteins regulate gene expression. This technology targets the cell organelles of the nuclei which store genetic information; mitochondria, which produce chemical energy; and ribosomes, which assemble proteins, using mRNA to make mitochondrial sequences.
A 2017 Gain-Of-Function research project from Germany, demonstrates how RNA extraction and quantitative reverse transcription-polymerase chain reaction or reverse genetics is used to knockout and knockdown genes using Hydra’s and CRISPR/Cas9.
The genetically modified Hydra lines in the Covid-19 operating system is first coded with chimeric gene sequences (Lentivirus) which is then being coded into human cells using CRISPR-Cas9 technology and electroporation.
Electrodes attached to gold programmable nanorobots transfect human cells, silencing your innate God-given genetic sequences and coding your cells to reproduce the synthetic genetic sequence of the chimeric spike protein (Lentivirus), indefinitely. More simply stated, your cells will continue to replicate themselves over and over again with the new genetic sequence of the chimeric pathogen you were injected with. The same chimeric pathogen was funded by bioterrorist Anthony Fauci and developed in Wuhan, China.
Parasites are also transfected with bacteria and used as transfection vectors for DNA binding and genetic sequencing in humans. Parasites can evade drugs, escape the immune system and regulate genes.
The human Malaria Genome Projectdeveloped at Stanford University, used CRISPR technology and bacterial plasmids which can replicate rapidly inside parasites. They transfected bacterial plasmids into parasites, disrupting a series of gene encoding molecules. In that study, scientists transfected Malaria parasites with Luciferase to use it for gene targeting and transgene expression in humans.
T. gondiiandP. falciparum and other parasites were also used in transfection studies. It’s important to be aware that from the P. falciparum they designed a Chloroquine-resistant transgenic parasite strain called Dd2.
LUCIFERASE
Hydra polyps are also being coded with the overexpressed chimeric proteincalled Luciferase, which is a Green Florescent Protein derived from the firefly. Transgenic Hydra also carries the Luciferase RNA trigger to code your cells with and silence genesin human cells.
Holstein lab investigated the repressing activity of HySp5 on the HyWnt3 promoter, performing Luciferase reporter assays in human HEK293T cells for DNA-binding and transplanting Hydra into humans by invading human tissues.
The transgenic Hydra and parasites replicate andmerge with humans during transfection. They are integrated with the transgenes (Luciferase and Lentivirus) into one of the epithelial cell lineages and assimilated into the human host. Thetransplanting of Hydra’s into humans is called Homoplastic transplantation using induced Hydranth as “implants”.
Epithelial cells are stem cell lineages responsible for cell signaling. Transgenic Hydra’s reporter genes are cell-signaling with each other inside humans, much like neurons in a neural network. Transgenic Hydra’s cell signaling becomes synthesized with human cell signaling in a process called catenin signaling, which is induced by mutations of genes in humans through upregulation (cell response) to the plasmids expressing activators in the Hydra (HySp5–2992:Luc); aka transfection.
Transgenic Hydra and parasites induce humans to generate a new electrochemical signal by organizing enzymes spatially to create a programmable redox enzymatic cascade pathway, changing the predictable generation of electrochemical signals in humans. The newly established synthetic gene sequences are now shared between the transgenic Hydra’s, parasites, and newly hybridized humans.
A team of scientists from UC Davis and Rice University was boasting back in July about manipulating the nervous system of Hydra Vulgaris and humans to “build a new brain from the bottom up”, in order to control neural pathways and human behavior. This technology was developed over the last decade through the Human Brain Project.
Graphene implants can record electrical activity in the brain at extremely low frequencies and over large areas, “unlocking the wealth of information found below 0.1 Hz”.
A Russian initiative called 2045 wants to use neural interfaces for an “improvement of man himself” because mankind is “standing at the edge of a total loss of the conceptual guidelines necessary for further evolution”. This demonstrates the anti-human mindset of eugenicists who want to clone the entire human race.
The fluorescent (Luciferase) Hydra’s were also tested with externally applied electrical fields to see how much voltage they could endure, to “facilitate the future use of electric fields as an experimental means to redistribute intracellular constituents in developing tissues”. I presume this was to test Hydra’s ability to survive 5G frequency?
THE OPERATING SYSTEM
Hydra’s and parasites also serve as a reporter system. Luciferase exhibits bright green fluorescence when exposed to light in the blue to the ultraviolet range, enabling the vaxxed to be traced externally. Genes of interest can be turned off occasionally or turned on at will by your patent holders through what’s called transregulation.
This means you’re not only externally traced 24/7but you’ll also be externally controlled. Your patent holders will be able to upregulate and downregulate your genetic codes through an external database, through the Eukaryotic Genome Annotation Pipeline for transgenic humans.
Did you think the Starlink satellite network’s “Precision Tracking Space System” had something to do with defense? Don’t worry, you’ll be “happy” owning nothing so long as they get your dopamine levels worked out.
ADDGene is selling a variety of CRISPR parasites to be used as gene vectors for human transfection. These are not “vaccines” at all but a WEAPONS SYSTEM (my words) for the RAPID CLONING (their words) of humans, through gene knockout (silencing), artificial gene sequencing (coding) and to monitor transfectants inside of humans (tracing).
ProSplign is a worldwide protein-to-genome alignment tool enabling Human DNA to be easily synthesized from a single-stranded RNA template and catalyzed by an enzyme for reverse transcriptase.
ADDGene also offers a Lentiviral Envelope and Packaging Plasmids for transfecting humans using transgenic Hydra. They offer“Non-overlapping NEURAL NETWORKS” (their words) using Hydra Vulgaris for building anew neural networkin Hydra’s. This technology is being deployed in humans through the Coivd-19 Quackccine program now.
Dr. Carrie Madej also disclosed in her latest interview on Stew Peter’s Show that the vaxxine operating system is building an artificial neural network in humans.
ADDGene offers a Tetracycline off system for on/off gene expression, “fusing tetR with the C-terminal domain of VP16 (virion protein 16), an essential transcriptional activation domain fromHSV (herpes simplex virus) which is being used for “reduced gene expression” in humans. This uses the chimeric E. coli bacteria and Lentivirus.
After Luciferase is infused and coded for targeted genes via a computer, it’s then mapped onto the Human through the public Galaxy server to perform “differential expression analysis”. Proteins can be targeted, upregulated, and downregulated.
Then there’s Vector Biolabs whose selling Adenovirus’ for human sp5 shRNA silencing. A Knockout vector system (adenovirus) for knocking down the expression of particular genes (gene silencing), is being marketed online and sold by Vector Builder. You can create artificial genome sequences and merge genomes of different species.
The Genome Data Viewer (GDV) will help you select genome assemblies (DNA sequences) for humans from primarily finished human clones, that were sequenced as part of the Human Genome Project.
VIGENE offers multiple shRNA cloning options for your gene silencing experiments. They’re packaging transfer Plasmids, Adenovirus’ (AAV) and Lentivirus’ and they guarantee at least a 70% knockdown of your gene of interest. They have a catalog of over 27,000 shRNA plasmid sets targeting the human genome.
This table lists common Lentiviral envelope and packaging plasmids that can be used with 2nd and 3rd generation lentivirus technologies.
ADDGene’s lentiviral genome is delivered to a target cell upon infection using CRISPR gRNA. They explain how the Lentiviral genome encodes genetic material that the “researcher” (or patent holders and Big Pharma) wants to be delivered to specific target cells. The genome is encoded by plasmids called “transfer plasmids,” which can be modified to encode a wide range of gene products.
ADDGene admits their DNA-targeting enzymes very often will delete, insert or otherwise alter the targeted RNA or DNA, so don’t let the fake media fool you.
Lentiviral Plasmids can be ordered through ADDGene here.
BEHAVIOR CONTROL
Vector Biolabs offers an Adenovirus (AAV) expressing shRNA for the knockout (gene silencing) of Human SP5. When developing this technology during the animal trials, social recognition, spatial learning, and memory were impaired after 4 weeks.
In an animal study using reverse transcriptase-polymerase chain reaction (RT-PCR) with an Adenovirus vector and drugs, scientists were able to induce Huntington’s Disease by targeting the Corpus striatum of the brain which resulted in 100 fold neurodegeneration and motor behavioral impairment.
REPRODUCTION & FERTILITY
The transgenic Hydra’s are used to induce gene silencing predominantly targeting embryonic cellsin the testes of men and the ovaries of women and also nerve cells. This is why we’re seeing neurological degeneration (PRION) after inoculation. It also explains why 82% of expectant mothers who take the “jab” are having spontaneous abortions.
Microinjection of foreign DNA into the pro-nucleus of single-cell embryos of fertilized mice to control the genetic expression of future generations has been perfected, since 2008.
Proteins control gene expression. Transgenic Hydra is instrumental in encoding the human SP5 (shRNAsilencing AAV) which is a gene on chromosome 2q31.1 that encodes a protein that binds to the GC-box promoter elements, thought to play a role in coordinating the intricate changes in transcription which occur in the developing embryo.
Wnt-3 is a protein that in humansis encoded by the WNT3gene. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis.
The point I’m making here is that the operating system is DNA-binding, downregulation, and upregulating genes using the transgenic Hydra’s, targeting human embryosand embryonic cells, leading to developmental alterations from binding genes to the Wnt/β-catenin signaling pathway.
Do you understand what this means? It’s not only the vaxxed who are being genetically modified, cloned, and hybridized, but SO ARE THEIR OFFSPRING! That is of course if you’re still able to reproduce at all after the jab! Most people will just be sterilized and their babies aborted. This is a human cloning experiment as well as extermination.
Microinjection of Retrovirus transgenes (Lentivirus & Luciferase) integrates randomly into the genome which poses enormous risks for the vaxxed as well as their hybrid offspring. This can create strange and unpredictable mutations of DNA by the addition of one or more base pairs. This is precisely why we’re seeing freaky mutations and why doctors are removing blood clots with Hydra-like tentacles from teenagers!
Dr. Carrie Madej shares an image of a blood clot with Hydra-like mutational growth that was removed from the heart of an early teen who received a Covid vaxx.
“It is a deadly protein” explains Dr. McCullough. “It is the first time in medicine that we are injecting vaccines and asking the human body to make a potentially lethal protein” .
While the Covid-19 serums appear on the surface to be only a clear liquid, under microscopy you can visibly see all the many components of the computer-interface operating system, which is a sophisticated biological weapons system for the cloning and extermination of the human race.
If you would like more information on detox protocols and disrupting the blood coagulation cascade which leads to blood clots from the jab or for protocols that will protect you from the adverse effects of transmission, please contact me directly at: metanutrients@mailfence.com
