via wikipedia:
“DNA teleportation is a claim that DNA produces electromagnetic signals (EMS), measurable when highly diluted in water. This signal can allegedly be recorded, transmitted electronically, and re-emitted on another distant pure water sample, where DNA can replicate through polymerase chain reaction despite the absence of the original DNA in the new water sample.[1] The idea was introduced by the Nobel laureate Luc Montagnier in 2009.[2] It is similar in principle to water memory, a concept popularised by Jacques Benveniste in 1988.[3]
No independent research has been conducted to support or refute the claim and, to this day, there is no know or plausible scientific mechanism by which it might work.[4]”
“In 2009, Montagnier and his collaborators published a paper titled “Electromagnetic signals are produced by aqueous nanostructures derived from bacterial DNA sequences” in which they reported that bacterial DNA can produce an electromagnetic signal (EMS) that is transferred through the cell culture medium.[2] In a medium of T lymphocytes (a type of white blood cell), they cultured bacterial DNA from Mycoplasma pirum and Escherichia coli. After filtering to remove all the bacteria, polymerase chain reaction was performed, which demonstrated the absence of remaining DNA. The solution was then incubated for two or three weeks, after which the presence of bacterial DNA was again detected. After serial dilution, they tested for electromagnetic radiation using a Fourier analysis technique developed by Jacques Benveniste and his team in 1996.[5] They detected electromagnetic frequencies only at high dilutions, ranging from 10−5 to 10−12.[2]
9 years ago:
7 months ago:
But is there any evidence of such technology being applied?
Well, so far all I could find is a 2015 patent:
Method for digital transduction of dna in living cells
via google patents:
“A system and method for inducing cytotoxicity, comprising a receiver configured to receive an electromagnetic signal from a container, using a receiver configured to capture electromagnetic emissions from the container over a frequency range of at least 100 Hz to 10,000 Hz; an amplifier configured to amplify the received electromagnetic signal; and an emitter configured to emit the amplified electromagnetic signal in proximity to living cells. DNA from a pathogen is amplified using PCR, purified, and serially diluted. Electromagnetic signals from the diluted DNA are received, and optionally stored. The receive signal is amplified and emitted in proximity to living cells, to produce under selected circumstances, a cytopathic effect.”
Can Our DNA Electromagnetically ‘Teleport’ Itself? One Researcher Thinks So
h/t JADR