NOTE: Sometimes the patents read ambiguously and in code language. They refer to the “Spike Protein” which is synonymous with the “Glycoprotein S”. Other times the descriptions could be referring to RNA and DNA changes, like coding new genetic sequences using “cDNA”. They sometimes read with words “in some embodiment’s” which likely means in some vials.
TABLE OF CONTENTS:
Moderna
Pfizer
Janssen (J & J)
Oxford University
AstraZeneca
GlaxoSmithKline (GSK)
Novavax
Gilead
MODERNA
“Lentivirus shows up in a couple of patents:Modernatx, Inc., Sars-Cov-2 mRNA domain vaccines November 4th, 2021.
The “Lentivirus” or “Lentiviral vector” is messenger RNA (mRNA) which contains the SARS, MERS, HIV 1-3 and SRV-1 Gain-and-Loss-of-Function bioweapons.
ASTRAZENECA AstraZeneca: Dapagliflozin and Ambrisentan for the prevention and treatment of covid-19 https://patents.google.com/patent/WO2021219691A1/en Lentivirus Not mentioned in the patent cDNA Not mentioned in the patent Deletion Not mentioned in the patent ORF Not mentioned in the patent
LentivirusNot mentioned in the patent cDNA Mentioned but seems only to refer to the formula. DeletionMentioned for mice. Probably just for preparation purposes. ORFNot mentioned in the patent
Stockholm University just released a scientific horror. The “spike” protein in the Covid-19 “vaccines” are penetrating the cells of the vaccinated, reaching the cell nuclei, and impairing your cell’s ability to repair damaged DNA.
Pharmaceutical “vaccines” are silencing the genes responsible for DNA repair and deleting them forever in humans.
Johnson & Johnson uses Adenovirus 26 (Ad26) in its vaxxine. J&J openly admits that their Ad26 vector “codes your cells to produce a spike protein”but they don’t tell you they’re also deleting your genes.
The U.S. patent #20140017278 for Adenovirus 26 and 35 Filovirus, openly states that it codes your cells with the Ebola and Marburg chimeric proteins.
“The filovirus antigenic protein is usually a glycoprotein from an Ebola virus or a Marburg virus.”
The J&J Adenovirus 26 vector deletes your E1 gene. The patent also states that it deletes the E1 gene in Humans. This is known as the X Chromosome. The E1 gene is required for accurate and instant repair of damaged DNA. Deletion of this gene is lethal.
E1 gene deletion causes embryonic lethality which means permanent sterility for men and women. It causes Lactic Acidosis in children which is the lack of oxygen in the blood. E1 gene deletion causes rapid cancer growth, Thrombosis, and the coagulation of the blood which leads to clotting. Blood clotting is the main reason people are dying from the Covid vaxxines.
E1 gene deletion causes Mitochondrial DNA-Associated Syndrome which is a process of glucose metabolism deficiency that exists in various diseases such as Alzheimer’s, epilepsy, diabetes-associated cognitive decline, and severe neurological disorders such as Leigh’s Syndrome. There’s a progressive loss of mental cognition and typically results in death within two or three years, usually due to respiratory failure.
You can order the chimeric messenger RNA of the Lentivirus and the Adenovirus 5 vectors or Baculoviridae online from Thermo Fischer, for recombinant cross-species genomics (cloning).
Thermo Fischer explains how the Adenovirus 5targets andentersthebronchial epithelial cells(lungs) and deletes the E3 and E4 genes, intentionally inducing Sjögren’ssyndrome which is long-term autoimmunity (AIDS).
Loss of your E4 gene deletes your cognitive function. Deletion of your E3 gene degenerates your brain, causes dementia, gradual loss of memory, judgment, and the overall ability to function.
The knockout of these genes affects the moisture-producing glands of your body. It’s not the “spike protein” that’s causing the blood of the vaxxed to coagulate, it’s the gene silencing (deletion). Without moisture, your blood coagulates and clots. The deletion of these genes also causes gastrointestinal disorders.
Adenovirus 5 also alters the cell signaling pathways and leads to Lymphoma due to destruction to the immune system. This causes cancers to grow and the blood to coagulate.
This is proof positive they’re creating the next “pandemic” with lethal injections that will gradually induce AIDS in the inoculated masses through gene deletion.
The pharmaceutical cartel has not only injected Ebola and Marburg into people but they’re alsotransfecting people’s cells with these catastrophic chimeric pathogens. The vaxxed will battle chronic infections and lifelong disabilities while the cells of the vaxxed continuously replicate with the synthetic genetic sequences of Ebola and Marburg until it kills them unless they detoxify continuously.
The immune system of the vaxxed is depreciating 5% each week according to a recent UK Government study. Everyone who vaxxed age 30 and above, will have no immunity left by Christmas. But that’s not all.
As the cells of the vaxxed replicate Ebola and Marburg “spike proteins” and their cells decay and die, they will shed the chimeric disease throughout the population via transmission. Therefore it’s crucial for the unvaxxed to continuously detoxify as well.
According to a UK government declaration from the NIH, we are presently in a Phase III clinical trial on Humans using the Adenovirus 5 vector to “fight Covid-19” which began on January 22, 2021.
“This is a global phase III clinical trial to evaluate efficacy, safety, immuogenicity of Ad5-nCoV manufactured by Cansino and Beijing Institute of Biotechnology in health adults aged 18 years old and above.”
So the UK Government is partners with the Chinese Communist Party (CCP) to exterminate Humans.
The World Health Organization (WHO) also published on their website that we are in an Ebola Vaccine Stage III Clinical Trial.
WHO published that we are in an Ebola Vaccine Stage III Clinical Trial
Viruses are still anunproven theory. Given the advances in scientific lab equipment and considering that we’re able to observe nanotechnology under microscopy and spectroscopy, would somebody please explain to me why we still can’t identify a virus? Could Germ Theory be the big pharmacopeia lie in modern medicine and Terrain Theorybe the more relevant truth?
Governments enhanced the airborne transmissibility in mammals (Humans) of highly virulent avian influenza strains. The history of making pathogens transmissible goes back at least to the synthesis of viable influenza H1N1from 1918. Incidentally, the 2009 swine flu Pandemicwas also induced by inoculation using the H1N1 vaxxine. So this is nothing new under the sun.
Sinister shadow governments have been weaponizing nature, producing diseases through vaxxine injection and genetically manipulating Humans for at least the past 100 years. But where did they get this technology to do it?
The U.S. National Library of Medicine revealed something rather interesting. The USSR’s ‘invisible anthrax’ is a Gain-of-Function bioweapon created by introducing an “alien gene“ into Bacillus anthracis (bacteria). That’s how they made Anthrax. They used an alien gene and genetically altered bacterial immunological properties to produce a deadly pathogen to Humans. Where did they get an alien gene from? A UFO crash perhaps? Negotiations with other beings? Your guess is as good as mine.
The U.S. Government has been testing this germ warfare technology on its own military troops since the 1950s, using Adenovirus 4, Ad5, and Ad7 vectors with HIV encoding Envelope (clade C.1086). The Ad7 vector delivered in enteric capsules has been used to“vaccinate” U.S. military personnel “against respiratory and gastrointestinal illness”, since the 1970s.
Monkeypox is also made from the same bacterial pathogens as Ebola and Marburg. Ebola and Marburg can kill nine out of ten people it infects. Although this is not really an infection, it’s transfection (human cloning).
Ebola and Marburgcause hemorrhagic fevers (VHF). They simultaneously affect multiple organ systems in the body and may be accompanied by hemorrhage, or bleeding. These pathogens cause high fever, chills, muscle aches, and vomiting. The patients worsen rapidly until they bleed from every orifice in their body, including needle puncture wounds. They usually die within 1-3 days.
Bill and Melinda Gates say on their Gavi website to expect the next pandemic to be a Marburg outbreak. These two psychics or psychos also claim that Ebola and Marburg are carried by African Green Monkeys.
Thelying CDC claimsthat people can get “Ebola Virus disease” through direct contact with an infected animal (bat or nonhuman primate). They’re taking the absolute piss out of us! Never in the history of medicine has an animal disease infected Humans! The only possible way to make a Human diseased with an animal disease is through cross-species genomics using Adenvirus or mRNA and Nanotechnology.
Polio vaccines used in the late 1950s and early 1960s were intentionally contaminated with a bacterial pathogen called the “Simian Virus” 40 (SV40) present in monkey kidney cells. The Simian Virus is used for infecting Humans.It was “accidentally administered to Humans” through Polio vaxxines.
The “Vaccinia virus” is similar to the “smallpox virus” but it’s not naturally occurring after all. Scientific Direct reported that “vaccinee-to-cattle and cattle-to-human Transmissions occurred on Farms”, proving the transmission of pathogens between animal to human species is being done by genetic engineering and administered through vaxxines.
Knocking out the E1 and E3 genes is necessary when transfecting cross-species in order to make the pathogen replicate. The Vaccinia pathogen has been used on a wide scale to produce many different kinds of chimeric proteins, including HIV-1 and it encodes approximately 250 genes.
Ebola and Marburg are GAIN-and-Loss-of-Function bioweapons and both are created using the “Green Monkey disease“, a chimeric pathogen that you can purchase online!
Adenovirus’ are from human/monkey clone origin and are used with chimeric Lentiviruses, as well as the Filoviruses. Of course, none of these are actual viruses! All the Adenoviruses and messenger RNA (mRNA) are chimeric weapons used to code your cells to reproduce deadly proteins used to both silence genes and program artificial genetic sequences. They are inducing diseases and making up disease names and syndromes to hide the fact that it’s coming from vaxxines!
Ebola, Marburg, and Monkeypox are Gain-of-Function bioweapons created using the “Green Monkey disease”. It’s an Adenovirus made from E. coli bacteria from the decaying flesh of a human/monkey hybrid’s kidney tissue culture. Adenovirus vectors transfect Humans withmonkey DNA, Ebola, and HIV. Adenovirus vectors are transfecting humans with monkey DNA and Human DNA from a Chimpanzee/Human clone to be exact.
There are 49 immunologically distinct types of adenovirus that can cause infection for long-term gene expression. They’re made with Sialic acid which is a group of derivatives of Neuraminic Acid found in animal tissues. Sialic acid is the primary entry receptor used in Adenovirus.
Sialic Acid is an animal DNA from “Species D” Adenovirus which is used in both Adenovirus 5 and Adenovirus 26 (Sinovac and J&J) to transfect Ebola and HIV into Human cells using Sialic acid-bearing glycans (animal DNA) as a primary cell entry receptor. Adenovirus 5 is of“Chimpanzee origin”. There’s that Green Monkey clone again!
Sialic acid proliferates tumor growth and metastases. N-acetylneuraminic acid (Neu5Ac) is made from E. coli bacteria. See the study’s here and here.
Polio vaxxines used in the late 1950s and early 1960s were “contaminated with a virus” or rather a bacterial pathogen called the Simian Virus 40 (SV40) which is present in monkey kidney cells used to grow the vaxxine.
The Pharma death cult is inducing diseases with their vaxxine racket and making up names and syndromes that they can then profit from by “treating” later when people become diseased. What would life be like without the Pharma cartel disabling our children and killing healthy people in the name of science and medicine?
There are no viruses involved in the making of any of the mRNA or Adenovirus vaxxines, only GAIN-and Loss-of-Function chimeric pathogens made from bacteria and other plasmids which Pharma keeps naming “viruses”.
There’s no “spike” from a virus particle being used in any of these vaxxine induced diseases. We should change our language from “spike protein” which is a half-truth with a half-lie and replace it with “chimeric protein” to be medically accurate because that’s what we’re dealing with.
E. coli bacteria are used as the base for all these chimeric diseases because bacteria DNA replicates. They’re also using other plasmids and mixing fungus, yeasts, and “several mammal-based systems” (Human/Chimpanzee clone), then genetically enhancing them to increase lethality.
They’re also using baculovirus-mediated insect cell expression. This means the Pharma cult is transfecting human cells with insect DNA. This could explain the strange mutations and Morgellons.
Marburg issimply Ebolawith Ricinadded to make it more lethal. Both cause hemorrhagic fevers (VHF) and attack multiple organ systems in the body, accompanied by bleeding.
The Pharma death cartel and the Eugenicists already have a PCR kit for “testing” for Marburg disease and a vaxxine to immunize against, called RiVax. The main component of RiVax is “a genetically altered version of a Ricin Toxin.” Ricin is more toxic than Graphene Oxide, by the way.
I think it’s high time people stop trusting our governments, stop relying on government and take our children out of public schools, as Dr. Zev Zelenko said to Alex Jones on Info Wars. Don’t sacrifice your kids to Satan.
My detox protocol works for the vaxxed and the unvaxxed to kill the Micro-plasmids (parasites, transgenic Hydra’s and bacteria) and reverse the coagulation cascade which leads to blood clots.
“That Thing” was discovered in the Covid Vaxx under microscopy by Dr. Carrie Madej and released on Stew Peter’s Show, on September 29th. It turned out to be a transgenic Hydra Vulgaris.
Because Pharma savages purposefully hide their injurious vaxxine ingredientsunder a trade secret, I knew the only way to get to the bottom of the mystery of why Hydras and parasites are in the Covid Vaxx, is to read through the peer-reviewed literature. A tedious job that even evades experts.
I appeared on the Stew Peter’s Show on October 27, to break my findings.
DOCTOR: HYDRAS AND PARASITES IN VAXX,TRANSFECTING HUMANS INTO NEW SPECIES
Transgenic Hydra lines were developed for GAIN-and Loss-of-Functionuse in humans at the Wuhan Institute in China and funded by Anthony Fauci, the NIH, and partly by DARPA. Karen Kingston revealed on Stew Peter’s Show that the patents holders are Israeli Zionists.
Hydras and parasites are being first transfected with chimeric pathogens using Plasmid DNA (E. coli bacteria and fungus) to produce a new genetically modified line of Hydras. They are coded with the synthetic genetic sequences of the Lentivirus and Luciferase. These are the infamous “spike proteins” that are being coded into human cells using the Covid-19 “vaccination” program.
Lentivirus is a combination of SARS, MERS, HIV 1-3, and SRV-1 (AIDS). Luciferase is a luminescent Green Flourescent Protein reporter system that allows for the 24/7 tracking of hybrid humans (the vaxxed) through an externalcomputer interface. These are GAIN-and-Loss-of-Function bioweapons.
Transgenic Hydra lines work as vectors, carrying the messenger RNA (mRNA) of the Lentivirus and Luciferase. The GMO Hydras polyps and parasite eggs are carried on the lipid coating of programmable nanoparticles which are delivered on Graphene Oxide sheets.
The coding of human cells with chimeric “spike proteins” through Reverse Genetics, is done by electroporation using programmable Gold Nanobots and CRISPR-Cas9. This technology is all part of an operating system that’s being shot into the veins of our children for the purpose of transfecting them with the most deadly pathogens ever created by governments.
Transgenic Hydra and parasites are assimilated into the human host through Homoplastic transplantation. Once human cells are coded with the artificial reporter genes, the cell signaling of the human alters permanently and synthesizes with the transgenic Hydras cell signaling, called Cantenin Signaling. The entire process of cloning ultimately constructs a new neural network and an artificial brainin humans, as well as a third strand to the DNA.
BLAST technology is being used to create new DNA sequences for cross-species genomics, and yes, this is cloning. The Covid Vaxx inserts an operating system enabling a computer interface that stores your internal data on an external database, for totalitarian control of transgenic humans (the vaxxed) using the Internet.
The operating system is gene silencing and knocking out the genetic sequences your patent holders don’t want you to have, while coding your cells with new, artificial genetic sequences through external interfaces. Essentially, they’re playing god’s. Your patent holders will be able to upregulate and downregulate your genetic sequences through external controls. This is called the “Hybrid Genome Assembly”.
The intended result of this genetic experiment is a mass die-off and rapid cloning of the human race to create an artificial hybridized species. Most people will become sterilized after Covid-19 inoculation and their lineage terminated, many will die and be exterminated because the human body cannot withstand this toxic experiment.
A small percentage of genetically cloned humans will be able to procreate but I strongly advise the vaxxed DO NOT PRODUCE OFFSPRING because they will not contain our God-given human genetic codes! Your offspring will not be human. If you want to have children for God’s sake, do not take the Mark Of The Beast. The operating system targets embryonic cells also cloning your offspring and thus hybridizing future generations. Cloned genetic mutations are always unpredictable so there is a great risk to your hybrid children.
A breaking news report from Mike Adams, The Health Ranger of Natural News, revealed a new scientific discovery that is indeed a “true horror”. Catch the Brighteon podcast here.
Stunning new research published in Viruses, part of the SARS-CoV-2 Host Cell Interactions edition of MDPI (Open Access Journals) reveals that vaccine spike proteins enter cell nuclei and wreak havoc on cells’ DNA repair mechanism, suppressing DNA repair by as much as 90%.”
Make no mistake about it humanity is facing a totalitarian biological attack using a very advanced weapons system that contains programmable nanobots and GMO’d microscopic organisms. Everything I’m reporting here is open-source, viewable online, and linked into my article on Red Voice Media entitled, What’s In the Vaxx? Transgenic Hydra And Parasite Implants Used As Rapid Human Cloning weapon system.
Dr. Christiane Northrop appeared on Gene Decode with Nicholas Veniamin to discuss detox protocols. Nicholas revealed that organic/synthetic insect DNA is also being used in the vaxx and this is what’s causing Morgellons.
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
