In further experiments, DNA fragment of HIV, taken from a long terminal repeat (LTR-sequence), has been used as a source of DNA. This fragment was amplified by PCR (487 bp) and nested PCR (104 base pairs) using special primers. In the first phase were created by DNA solutions, where was the production of EMC in the external electromagnetic environment. Further, the following steps were taken. As shown in Figure 3, one of the benefits of raising (Let's say 10-6) It was placed in a container, a protected layer of mu-metal thickness of 1 mm (which reduces the absorption of excess low-frequency waves). There was another test tube, containing pure water. Water contents of each tube was filtered through 450 nm and 20 nm filters and diluted from 10-2 to 10-15. Around them was a copper solenoid, generating an electrical current of low intensity, with a frequency of about 7 Hz, produced by external generator.
The produced magnetic field was maintained for 18 hours at room temperature. Then EMC were recorded for each test tube. It turned out, as the blood collection tube, containing only water, emits the EMC dilutions, sootveKDtvuûŝih positive EMC in the original tube with DNA.
These results show, that with regard to the transfer of 7 Hz. oscillations, originally initiated by the original DNA nanostructure, occurs in clean water. It was found, the following restrictions inhibit the transfer of EMC to the tube with water: (PG: controls!)
The dwell time of less than two tubes 16 - 18 hours
No spiral
Off the magnetic field generator
Excitation frequency < 7Hz
Absence of DNA in tube 1.
At this stage is the most critical step was taken, a study of features of water of nanostructures, subjected to impact by reviving one DNA sequence. To do this, all the ingredients to create a DNA polymerase chain reaction (nucleotides, the primers, the polymerase) were added to the tube with water-recipient. Development took place while the classic conditions (35 cycles) in termociklere. The DNA was further electrophoresis in agarose gel. The plot was discovered DNA the estimated size of the initial slice long terminal repeats.
Further confirmed, the sequence of the DNA matches or nearly matches the initial sequence of DNA long terminal repeats. Actually, It coincides 98% (raznitsa in two nucleotides) of 104. This experiment was highly repeatable (12 of 12) and was also duplicated with another sequence the DNA of bacteria Borrelia burgdorferi, causative agent of Lyme disease. It was clearly shown, that water nanostructures and their electromagnetic resonance can surely save DNA. the elements support interesting explanation of our experiment on filter Mycoplasma pirum (Fig. 1): nanostructures, caused by DNA (M). pirum in filtered water, represent various segments of its genomic DNA. Each nanostructure on contact with human lymphocytes retro transkribirueKDâ sootveKDtvuûŝej DNA in some cellular DNA-polimerazami. Next, There is a certain probability (even very low), that each piece of DNA to be reunited in the same cage with other fragments to reconstruct the entire genome DNA. You must allow, that eukaryotic cells synthesis component of mycoplasmas (membrane lipids, Ribosomes) can also be carried out DNA Mycoplasma. The only set of cells of Mycoplasma full enough to produce infection of lymphocytes. Recent experiments Group G. Vinter revealed [5], the synthetic genome DNA is capable of supporting all of the properties of the Mycoplasma. All the steps, taken in the field of regeneration of water, You can analyse and check.
