Brain Eating Nanobots Being Put in Vaccines

[Breaking News Breaking News]

Incredible information here about nanotechnology being put in the vaccines to attack your brain!  Make sure you read all of the the original article.  Before anybody thinks that they could never make something that would change your personality by attacking your brain, I point you to this video below that shows a man at the Pentagon calmly explaining how a virus they are creating will attack the “God Center” of the brain and destroy it!  He tries to sell it by saying that this will stop suicide bombers by people that believe in God but of course this is just the sell job.   He says it will take somebody that believes in God and turn them into a “normal” person!  So if you’re a Christian it will make you no longer believe in God and Jesus Christ which is your key to eternal life!  This is the pure evil that is the new world order government running the US!   I do not know if this man has correct information but because of the video below I think it bears further consideration!  Personally, I will never get any vaccines because of the evil men in charge of the medical system!

 
Pentagon Briefing where presenter brags about a new virus they created that attacks the “God” center of the brain!

http://www.youtube.com/watch?v=spw5nmUrpWA

NO MATTER WHAT the story, DO NOT get vaccinated, a new bioweapon is being distributed via vaccines
Ebola outbreak likely another “swine flu” scare
HERE IS THE CHALLENGE:

I challenge ANYONE, ANYONE AT ALL, to come up with a printed book from the 1990′s that has the six legged T4 (proven Israeli Nanobot) bacteriophage in it, as pictured to the left. The web can be faked with ease. You cannot fake print. Let’s see it ON PAPER, in unchangeable print from the 1990′s. PRINT OR THIS THING CAME FROM AN ISRAELI LAB IN 2007, as I state and present compelling evidence for in the T4 nanobot report below.
 
There have been many reports about nanobots being developed that will destroy people. This report actually identifies that nanobot and what it is based upon. Once this nanobot is received via a tainted vaccine, it inserts DNA into your cells which instructs your own cells to produce more copies of itself and THAT is how it replicates. And it NEVER backs off, it simply orders your own cells to keep producing it until your cells die from being over worked doing exactly that. And it’s completely verified this thing came from a lab in 2007, scroll down to the pictures if you don’t want to read a lot.
Anti vaccine alternative news web sites are being taken down RIGHT NOW, with simultaneous total purges of the Google cache within hours and I beg to question why.
 
Actually, there is little to question. The answer is apparently obvious. The elite are now going for a huge push to get the T4 bacteriophage nanobot and other tainted vaccine additives put into the entire world public via mandated injections AT ONCE. And I suspect they are going to use a phony Ebola outbreak to scare the people into accepting shots laced with T4 nanobots, with everyone receiving the shot within a short period of time.
 
More so than flight370, Ukraine, and other issues, the takedown of anti vaccine web sites right in the middle of an “Ebola outbreak” is the coincidence we should all be paying attention to, THIS IS THE NEWS, if we miss this one we are likely to be destroyed.
Anyone who is with it enough to find a web site like this one ought to know about the NWO plan for global depopulation and the establishment of compact slave cities that can be managed with ease. What better way could there be to manage a massive depopulation than a fake outbreak, with the real disease being in mandated shots, peddled as vaccines that are supposed to protect? You can bet the elite do not want to actually release something that could kill them into the wild in the form of a real outbreak. They would instead opt to use all their ill gotten tax dollars to formulate a shot and inject it into their victims, with a certain percentage of the shots being non hazardous, perhaps 1 in 10, and the rest representing the end of life for the recipient. If the disease is a managed disease that is completely non contageous and can only be received via a shot, they can rest easy while the world dies around them.
 
And THIS is why they are pushing vaccines so hard, and now actively working to destroy completely legitimate dissent. I am certain that my web site is only staying online because it got too well known too quickly to take down without making waves, and I am going to use that advantage to warn the people and hope for the best.
 
Note by Glenn:  I found a good video that shows how this T-4 nanobot would infect your DNA and destroy you.  

 
THE EBOLA OUTBREAK IS LIKELY A HOAX TO TRICK YOU INTO GETTING A VIRAL NANOBOT LACED VACCINE THAT WILL DESTROY YOU
 
 
RED ALERT REPORT: CONFIRMED: VIRAL NANOBOTS A REALITY AND OUT IN THE WILD NOW
A NOTE TO THE SHILLS: What will happen if you end up with these things inside you? These are NOT Iphones, WANNA SHILL THIS? ARE YOU SURE YOUR ISRAELI LAB GOT THIS RIGHT AND THESE WILL NEVER GET INTO YOU?
With only 183K of super efficient DNA code, viral nanobots were released into the wild via vaccinations on September 22 2007 and are being peddled as a natural variant of the T4 bacteriophage. But this report PROVES THESE NANOBOT PHAGES ARE NOT NATURAL, AND WERE INSTEAD CREATED BY ISRAEL. These nanobots invade host organisms or cells and insert DNA that causes the host make more nanobots until the host organisms or cells die from overexertion producing them. THESE ARE LIKELY TO BE IN THE PAPALOMA VACCINE, FLU SHOTS AND OTHER VACCINATIONS, VACCINES WILL BE THE DELIVERY MEDIUM THESE ARE DISTRIBUTED WITH. These are most likely in Gardasil, which in fact appears to be designed to destroy the feminine emotional centers and attack the brain, and this report proves it.
 
If you are a headline skimmer who can’t get past the first page of reading, you had better reconsider your information gathering habits and READ THIS IN FULL.
Brain destroying Genetically Modified six legged T4 bacteriophage is a NANOBOT
Vaccines being used for distribution RIGHT NOW
 
Note by Glenn:  Make sure you read the source article for full details.  Again, everybody must make their own decisions about vaccines.  I’m not a doctor and cannot give you medical advice.  All I’m saying is that evil men control the medical system and they already have a virus that can change your brain so you no longer believe in God!  They brag about this in the first video I posted on this article.  I’ve made a decision myself to not take any vaccines no matter what the liars in our government tell me.  I put my faith in God no matter what story they create and put on the fake news!
 
Full Article:
http://www.jimstonefreelance.com/phages.html

[Vmedvil]

Synthetic Viral Synthesis

Step I:Custom Oligonucleotide Synthesis
Materials
•Commerical Nucleic Acid Synthesizer
•Solution of the four DNA phosphoramidite monomers (bases)
•All the 5’-hydroxyl groups must be blocked with a DMT group for all four bases
•All phosphorus linkages must be blocked with a cyanoethyl group.
•Blocking solutions
•Reaction chamber and a type of solid support such as controlled pore glass
•The solid support should be prepared with the desired first base already attached via an ester
linkage at the 3’-hydroxyl end.
•Dichloroacetic acid or trichloroacetic acid
•Tetrazole
•Acetic anhydride and N-methylimidazole
•Dilute iodine in a water/pyridine/tetrahydrofuran solution
•Concentrated ammonia hydroxide.
•Materials for one desalting method
Process
Step A: De-blocking
The first base, which is attached to the solid support, is at first inactive because all the active sites
have been blocked or protected. To add the next base, the DMT group protecting the 5'-hydroxyl
group must be removed. This is done by adding a base, either dichloroacetic acid (DCA) or
trichloroacetic acid in dichloromethane (DCM), to the reaction column. The 5’-hydroxyl group is now the only reactive group on the base monomer. This ensures that the
addition of the next base will only bind to that site. The reaction column is then washed to remove
any extra acid and by-products.
Step B: Base Condensation
The next base monomer cannot be added until it has been activated. This is achieved by adding
tetrazole to the base. Tetrazole cleaves off one of the groups protecting the phosphorus linkage.
This base is then added to the reaction column. The active 5’-hydroxyl group of the preceeding
base and the newly activated phosphorus bind to loosely join the two bases together. This forms
an unstable phosphite linkage. The reaction column is then washed to remove any extra
tetrazole, unbound base and by-products.
Step C: Capping
When the activated base is added to the reaction column some does not bind to the active 5’-
hydroxyl site of the previous base. If this group is left unreacted in a step it is possible for it to
react in later additions of different bases. This would result in an oligonucleotide with a deletion.
To prevent this from occurring, the unbound, active 5’-hydroxyl group is capped with a protective
group which subsequently prohibits that strand from growing again. This is done by adding acetic
anhydride and N-methylimidazole to the reaction column. These compounds only react with the
5’-hydroxyl group. The base is capped by undergoing acetylation. The reaction column is then
washed to remove any extra acetic anhydride or N-methylimidazole.
Step D: Oxidation
In step 2 the next desired base was added to the previous base, which resulted in a unstable
phosphite linkage. To stabalize this linkage a solution of dilute iodine in water, pyridine, and
tetrahydrofuran is added to the reaction column. The unstable phosphite linkage is oxidized to
form a much more stable phosphate linkage.
Repeat as need based on length desired between 1 and 10,000 times.
Final Product: DNA Chains from 1 to 10,000 base pairs in length.
Step II:Molecular Cloning: Polymerase Chain Reaction(PCR)
Materials
-Thermal Cycler
-Taq polymerase
-Generated DNA Fragments
Process
A. Denaturation - the DNA is heated usually to 95C to render it single-stranded
B. Annealing - the two primers bind the appropriate complementary strand; the temperature for
this step varies depending on the of size of the primer and its homology to the target DNA
C. Primer Extension - DNA polymerase extends the primer by its polymerase activity; this is
done at a temperature optimal for the particular polymerase that is used; currently the most
popular enzyme for this step is Taq polymerase, the DNA polymerase from the thermophilic
("heat-loving) bacteria Thermus aquaticus; the extension is performed at 72C. These steps are
repeated from 28-35 times. Since the reaction is essentially exponential and since each cycle is
about 5 minutes, a large quantity of DNA can be produced for analysis in as little as several
hours.
Final Product: Exponential DNA cloning
Step III:Mass Ligation Reaction
Materials
•Two or more fragments of DNA that have either blunt or compatible cohesive ("sticky") ends.
•A buffer which contains ATP. The buffer is usually provided or prepared as a 10X concentrate
which, after dilution, yields an ATP concentration of roughly 0.25 to 1 mM. Most restriction
enzyme buffers will work if supplemented with ATP.
•T4 DNA ligase. A typical reaction for inserting a fragment into a plasmid vector (subcloning)
would utilize about 0.01 (sticky ends) to 1 (blunt ends) units of ligase.
Process
The optimal incubation temperature for T4 DNA ligase is 16C and when very high efficiency
ligation is desired (e.g. making libraries) this temperature is recommended. However, ligase is
active at a broad range of temperatures, and for routine purposes such as subcloning,
convenience often dictates incubation time and temperature - ligations performed at 4C overnight
or at room temperature for 30 minutes to a couple of hours usually work well.
Final Product: Every possible recombination
Step IV:Activation and Reproduction:Plasmid Vector
(sub-cloning)
Materials
-Anything with ribosomes
-NotI Ligase
Process
Same as step III
Final Product: Viral Vector