Tag: dna

DNA Contamination in Pfizer COVID Shot 500 Times Permissible Level: New Study

Genetic impurities in the Pfizer mRNA COVID vaccine could be as high as 500 times the permissible limit, according to a new study.

In the study, published in Methods and Protocols, two German researchers raise worrying questions about the reliability of the quantitative PCR technique used by Pfizer-BioNTech to measure DNA contamination in the vaccine.

Using their own tests on the vaccine’s lipid nanoparticles, they discovered levels that were between 360 and 534 times higher than the 10 nanogram per dose limit set by regulators.

The researchers argued that the methods used by Pfizer-BioNTech test for only 1% of the original DNA template used to make the vaccine, meaning that 99% of the genetical material from the template therefore goes untested and potentially undetected.

Similar concerns have been raised by other researchers.

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Pfizer’s Covid Gene Therapy Shots Have Over 500 Times Allowable Levels of DNA Contamination — Study

A study published this month has found that the Pfizer mRNA Covid ‘vaccine’ gene therapy injections contain DNA contamination at over 500 times allowable levels, raising fears that the DNA may integrate into the vaccinated person’s own DNA, causing mutations that can lead to diseases such as cancer.

“The available information and data indicate that the ready-to-use mRNA vaccine Comirnaty contains DNA impurities that exceed the permitted limit value by several hundred times and, in some cases, even more than 500 times,” the study said in the ‘Conclusions’ section.

Modified messenger RNA (mRNA) vaccines work by encapsulating the RNA sequence of the Covid spike protein (the dangerous part of Covid, linked to HIV) into lipid nanoparticles which are able to deliver the RNA payload into the body’s cells. The RNA is then integrated into the person’s genetics so they will produce the Covid spike protein, which the body can then develop an immune response to.

However, according to the study, mRNA is not the only genetic information being injected into people.

“…in addition to the mRNA active ingredient, DNA impurities are also encased in lipid nanoparticles and are therefore difficult to quantify,” the study said in the ‘Abstract’ section.

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Toddler Dies in Pfizer Gene Therapy Trial

Yesterday I republished a video and article entitled, “What Happened to Their Babies,” describing the lack of ethics and grossly inhumane experimentation that Pfizer conducted on babies and toddlers with their COVID-19 mRNA gene-editing injections.

Just a few hours ago, multiple industry outlets began breaking this official statement from Pfizer that a toddler died of a cardiac arrest in an investigational trial of boys, aged 2 to 4 year olds, to treat a rare form of muscular dystrophy with a recombinant adenovirus gene editing technology.

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COMPANY CLAIMS ITS ‘DIRECTED EVOLUTION’ MICROBIOME-ENHANCED PLANTS LITERALLY EAT POLLUTION FOR BREAKFAST

Bioengineering R&D company Neoplants says its ‘directed evolution’ houseplants can clean the air inside your home 30 times more efficiently than an ordinary houseplant. This is due to genetically engineered bacteria that convert some of the most common and dangerous indoor air pollutants, known as Volatile Organic Compounds (VOC), into biodegradable components like sugar that the plant ultimately consumes as food.

This means harmful pollutants Benzene, Toluene, and Xylene, which can reach as much as five times (or even up to 100 times) the concentration indoors as they do outdoors, are not only filtered out of the air, but their breakdown products are used to feed the plant itself, thereby “turning a harmful and commonly found chemical in your home into a healthy source of fuel for the plant.”

“It harnesses the power of nature to purify indoor air from 3 of the most carcinogenic pollutants we find in every home, up to 30 times better than any regular houseplant,” explained Lio Mora, Neoplants CEO, and co-founder, in an email to The Debrief.

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US company hoping to bring back the dodo and the mammoth – but here’s why it won’t be like Jurassic Park

The idea of scientists bringing pre-historic creatures back to life with some clever DNA trickery might sound familiar to fans of the 1993 Hollywood blockbuster Jurassic Park.

But for Colossal Biosciences – a company that hopes to reintroduce extinct species such as the dodo and the mammoth – it is more than just a film script.

It’s a reality – and one that could be just years away.

“We’ve got all the technology we need,” says Ben Lamm, chief executive of the firm, based in Dallas, Texas.

“It is just a focus of time and funding. But we are 100% confident [we can bring back] the Tasmanian tiger, the dodo, and the mammoth.”

The science behind the project is simple: Work out the genes that make an extinct animal what it is, and then replicate those genes using the DNA of a close existing relative.

“It’s almost reverse Jurassic Park,” says Mr Lamm, speaking to Sky News.

“In the film, they were filling in the holes in the dinosaur DNA with frog DNA.

“We are leveraging artificial intelligence and other tools to identify the core genes that make a mammoth a mammoth and then engineering them into elephant genomes.”

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Genetic Analysis Bolsters Blackfoot People’s Land Claims

The advancement of DNA collection-and-analysis technology has had significant consequences for anthropology and archaeology, resulting in surprising revelations about genetic connections between modern populations and ancient peoples. In the latest example of this fascinating phenomenon, a team of genetic scientists, in collaboration with representatives of the indigenous Blackfoot nation, have just completed a study that establishes an unexpected relationship between modern Blackfoot people and some of the earliest inhabitants of the Americas.

“We show that the genomics of sampled individuals from the Blackfoot Confederacy belong to a previously undescribed ancient lineage that diverged from other genomic lineages in the Americas in Late Pleistocene times,” the scientists and their Native American colleagues wrote in an article published in the journal Science Advances. “Using multiple complementary forms of knowledge, we provide a scenario for Blackfoot population history that fits with oral tradition and provides a plausible model for the evolutionary process of the peopling of the Americas.”

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Scientists Put Tardigrade Proteins Into Human Cells. Here’s What Happened.

Freeze ’em, heat ’em, blast them into empty space; with survival skills unlike any other organism on the planet, those hardy critters known as tardigrades will only come back for more.

While it’s clear their ability to withstand stress is in part due to their ability to turn their insides into gel, the mechanisms behind this act of metabolic preservation haven’t yet been made clear.

A new study led by researchers from the University of Wyoming found that expressing key tardigrade proteins in human cells slowed metabolism, providing critical insights into how these virtually indestructible invertebrates can survive under the most extreme conditions.

The team focused on a particular protein called CAHS D, already known to protect against extreme drying (desiccation). Through a variety of methods, the researchers showed how CAHS D transformed into a gel-like state when under stress, keeping molecules protected and protecting against drying.

“This study provides insight into how tardigrades, and potentially other desiccation-tolerant organisms, survive drying by making use of biomolecular condensation,” write the researchers in their published paper.

“Beyond stress tolerance, our findings provide an avenue for pursuing technologies centered around the induction of biostasis in cells and even whole organisms to slow aging and enhance storage and stability.”

Tardigrades have already shown they can survive hot and cold temperatures and high levels of radiation that would be fatal to human beings, and long periods without any water – normally so essential to life. They can even survive in space.

Previous research has revealed an impressive number of tricks that tardigrades use to stay alive, built up over hundreds of millions of years. Essentially, they’re very good at slowing the processes of life right down with the help of CAHS D, and that could be useful in human cells too.

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Three Pennsylvania men who have spent decades in prison for rape and murder of elderly woman in her home have their convictions overturned

Three Pennsylvania men who were imprisoned for decades in the 1997 slaying of a 70-year-old woman – despite their DNA never matching that found at the scene – have had their convictions overturned by a judge.

The Delaware County judge threw out the convictions for Derrick Chappell – who was 15 when he was arrested – and first cousins Morton Johnson and Sam Grasty. The District Attorney is now reviewing the case to see if a new trial is necessary.  

Chappel, Johnson, and Grasty were each convicted in separate trials for the murder of Henrietta Nickens, a 70 year old woman who was brutally killed at her home in Chester, Pennsylvania, on October 10, 1997.

Nickens was savagely beaten and had had her underwear removed. Investigators found her home ransacked and blood on the walls and bedding. 

A mysterious green jacket, in the pocket of which was cocaine, was found on top of Nickens’ television set.

Investigators discovered semen in the woman’s rectum. They tested the semen and found that it didn’t belong to any of the three arrested individuals.

The prosecutors, who have been characterized as pugnacious, sought to separate the recovered semen from the crime. They affirmed that the semen might have originated from consensual intercourse and was unrelated to the murder. 

Nickens had been chronically ill and had no known sexual partners. 

The prosecution’s case against Chappel, Johnson, and Grastly hinged on the testimony of key witness Richard McElwee, who was 15 years old at the time of the crime.

McElwee testified that he functioned as a lookout while the three older boys pilfered Nickens of $30.

In exchange for his testimony, McElwee pled guilty to third-degree murder, as well as other charges. He was sentenced to serve six to 12 years in prison in 1999.

In 2000 and 2001, Chappel, Johnson, and Grasty were each convicted of second-degree murder, and they were sentenced to life in prison.

Over the course of their more than two decades-long prison stint, the three men have continued to protest their innocence.

Each of them filed pro se petitions in federal court over the years saying they were wrongly convicted, but their petitions were denied.

The fate of Chappel, Johnson, and Grasty drew the attention of many organizations dedicated to freeing wrongly convicted men and women.

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Scientists Close To Controlling All Genetic Material On Earth

Scientists at the University of Pennsylvania’s Perelman School of Medicine have developed a new method to create human artificial chromosomes (HACs) that could revolutionize gene therapy and other biotechnology applications. The study, published in Science, describes an approach that efficiently forms single-copy HACs, bypassing a common hurdle that has hindered progress in this field for decades.

Artificial chromosomes are lab-made structures designed to mimic the function of natural chromosomes, the packaged bundles of DNA found in the cells of humans and other organisms. These synthetic constructs have the potential to serve as vehicles for delivering therapeutic genes or as tools for studying chromosome biology. However, previous attempts to create HACs have been plagued by a major issue: the DNA segments used to build them often link together in unpredictable ways, forming long, tangled chains with rearranged sequences.

The Penn Medicine team, led by Dr. Ben Black, sought to overcome this challenge by completely overhauling the approach to HAC design and delivery. “The HAC we built is very attractive for eventual deployment in biotechnology applications, for instance, where large-scale genetic engineering of cells is desired,” Dr. Black explains in a media release. “A bonus is that they exist alongside natural chromosomes without having to alter the natural chromosomes in the cell.”

To test their idea, the scientists turned to a tried-and-true workhorse of molecular biology: yeast. They used a technique called transformation-associated recombination (TAR) cloning to assemble a whopping 750 kilobase DNA construct in yeast cells. For context, that’s about 25 times larger than the constructs used in previous HAC studies. The construct contained DNA from both human and bacterial sources, as well as sequences to help seed the formation of the centromere.

The next challenge was to deliver this hefty payload into human cells. The team accomplished this by fusing the engineered yeast cells with a human cell line, a process that had been optimized in previous studies. Remarkably, this fusion approach proved to be much more efficient than the traditional method of directly transferring naked DNA into cells.

The results were stunning. Not only did the engineered HACs form successfully, but they did so with much higher efficiency compared to standard methods. Furthermore, these designer chromosomes were able to replicate and segregate properly during cell division, a key requirement for their long-term stability and functionality.

“Instead of trying to inhibit multimerization, for example, we just bypassed the problem by increasing the size of the input DNA construct so that it naturally tended to remain in predictable single-copy form,” explained Dr. Black.

But the researchers didn’t stop there. They also devised a clever way to visualize the HACs in their native, uncompacted state. By gently lysing the cells and using a special centrifugation technique, they were able to isolate the HACs away from the rest of the cellular DNA. This allowed them to confirm that the HACs maintained their single-copy status and circular topology, without any unwanted rearrangements or additions.

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China Used COVID-19 PCR Tests to Acquire Millions of Americans’ DNA

Several bombshell US government and intelligence agency reports confirm that China used COVID-19 PCR tests to legally collect DNA from Americans and millions of adults and children across 180 countries.

On October 26, 2021, my son was administered a COVID-19 PCR test at his school without my consent. I immediately looked into the San Diego School District’s “COVID-19 testing program” and discovered that the NIH was funding the testing as a “research program” being conducted by GenBody, a South Korean diagnostics company in order to collect the DNA of American children and then transfer their genomic data to foreign nations. On October 27, 2021, on Stew Peters, I repeatedly stated that my son’s DNA was collected and transferred to a foreign nation as part of a NIH-funded foreign study under the farce of public health safety. View 5:20 – 8:15.

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