Vaccines are in scriptures

 

Revelation 18:

23 - And the light of a candle shall shine no more at all in thee (No Holy Spirit);

and the voice of the bridegroom and of the bride shall be heard no more at all in thee: (Your DNA will be changed)

for thy merchants ( Bill Gates, Trump) were the great men of the earth;

for by thy sorceries (medicines/vaccinations, poison) were all nations deceived.

 

Strong's G5331 - pharmakeia

†φαρμακεία pharmakeía, far-mak-i'-ah;

from G5332; medication ("pharmacy"),

i.e. (by extension) magic (literally or figuratively):—sorcery, witchcraft.

 

The use or the administering of drugs, poisoning, sorcery, magical arts,

often found in connection with idolatry and fostered by it

 

metaph. the deceptions and seductions of idolatry

 

A virus is a small collection of genetic code, either DNA or RNA, surrounded by a protein coat.

A virus cannot replicate alone.

 

It has to be injected

 

Do NOT use your SSnumber you cannot by or sell without it anymore. (Revelation 13:17)

It is the PERSON = SIN in james 2:9 Deuteronomy 1:17

Get out of the Babylon system. (Revelation 18)

 

Revelation 13:

17 And that no man might buy or sell, save he that had the mark (Quantum Dot Vaccine Mark) , or the name (Luciferace) of the beast, or the number (Bismillah [in the name of Alah; oath, curse], 666, unmarried) of his name.

 

QDVM:

 

James 2:

But if ye have respect to persons, ye commit sin, and are convinced of the law as transgressors.

 

Deuteronomy 1:

17 Ye shall not respect persons in judgment; but ye shall hear the small as well as the great; ye shall not be afraid of the face of man; for the judgment is אֱלֹהִים and the cause that is too hard for you, bring it unto me (Moses) , and I will hear it.

 

Psalms 116:

13 I will take the cup of salvation (Yahushua), and call upon the name of the יְהֹוָה

 

Isaiah 33:
22 For the יְהֹוָה is our judge (שָׁפַט), the יְהֹוָה is our lawgiver (חָקַק), the יְהֹוָה is our king (מֶלֶךְ); he will save us.

 

Vaccines are Not Kosher

Messiah's body the implementation of the Mark is before us.

Source:

Academy News - Another Form of the Mark of the Beast - JOIN US!

Source:

 

Luciferase Immunoprecipitation System (LIPS) assay is a rapid, simple, and sensitive test to detect antibody response to respiratory syncytial virus

 

Researchers at the U.S. Food and Drug Administration (FDA) have developed a simple, rapid, and sensitive test that identifies individuals who have made antibodies against respiratory syncytial virus (RSV), the most common cause of serious lower respiratory tract infection in infants and young children worldwide. RSV also affects many elderly individuals, especially those with underlying heart or lung disease, accounting for nearly as many hospitalizations as influenza.

 

The development of the new assay is important because it could be a valuable tool for assessing the efficacy of RSV vaccines during clinical trials since it can help to identify individuals infected with RSV following a winter season.  Since many of the current candidate vaccines contain or express only one or a few of the proteins found in the virus, antibody responses to non-vaccine RSV antigens can serve as a marker of exposure and infection in subjects given these vaccines. 

 

An important advantage of the new test, called a Luciferase Immunoprecipitation Systems (LIPS) assay, is that it is less complicated and easier to perform than other assays now available. Moreover, unlike some currently used tests, it readily differentiates immune responses against the two major subtypes of RSV, RSV-GA and RSV-GB.

 

The LIPS assay detects antibodies against G glycoprotein, (G protein), a molecule that occurs on the surface of the virus.  To develop the assay, the FDA scientists genetically engineered RSV G proteins from both subgroups. They tagged each G protein with luciferase, an enzyme that interacts with a protein called luciferin to release light

 

The luciferase-tagged G proteins (RSV-GA and RSV-GB) acted as “bait” to antibodies against the G proteins in samples of human serum (the clear fluid of blood without red or white cells), causing them to bind to the tagged proteins. The scientists added special protein beads that bind the antibodies with the luciferase-tagged G proteins to the bottom of a plastic test well. Then they added luciferin and measured the amount of light released when it interacted with luciferase, which enabled them to calculate how strong the antibody response was to the G proteins. (How much of the HOLY Spirit is within you)

 

The FDA scientists showed that the LIPS assay could specifically detect anti-RSV-GA and -GB antibodies in mice that had been infected intranasally with RSV-A or -B strains. In addition, the assay detected antibodies against either RSV-A or RSV-B in samples taken from infants who had contracted the disease—depending on which subtype was present. The assay also found that serum from adolescents had antibodies against G proteins from both subtypes, suggesting that adolescents had been exposed to both RSV-A and RSV-B by that time in their lives.

 

Title

Development of Luciferase Immunoprecipitation Systems (LIPS) Assay to Detect IgG Antibodies against Human Respiratory Syncytial Virus G-Glycoprotein

Vaccines 2019, 7, 16; doi:10.3390/vaccines7010016

 

Authors

Roberta Lynne Crim, Sangeeta Kumari , Priyanka Jayanti , Susette Audet, Ashwin Kulkarni § and Judy Beeler *

Office of Vaccines Research and Review, CBER, FDA, Silver Spring, MD 20993, USA;
roberta.crim@fda.hhs.gov (R.L.C.); sk4px@virginia.edu (S.K.); pjayanti94@gmail.com (P.J.);
susette.audet@fda.hhs.gov (S.A.); schwinn6@gmail.com (A.K.)

* Correspondence: judy.beeler@fda.hhs.gov; Tel.: +1-240-402-9389
† Present affiliation: ATCC Cell Systems, Gaithersburg, MD 20877, USA.
‡ Present affiliation: Systems Planning and Analysis, Alexandria, VA 22311, USA.
§ Present affiliation: BioHealth Innovations Inc., Rockville, MD 20850, USA.

 

Source: 

 

G protein

G proteins, also known as guanine nucleotide-binding proteins, are a family of proteins that act as molecular switches inside cells, and are involved in transmitting signals from a variety of stimuli outside a cell to its interior. Their activity is regulated by factors that control their ability to bind to and hydrolyze guanosine triphosphate (GTP) to guanosine diphosphate (GDP). When they are bound to GTP, they are 'on', and, when they are bound to GDP, they are 'off'. G proteins belong to the larger group of enzymes called GTPases.

There are two classes of G proteins. The first function as monomeric small GTPases (small G-proteins), while the second function as heterotrimeric G protein complexes. The latter class of complexes is made up of alpha (α), beta (β) and gamma (γ) subunits.[1] In addition, the beta and gamma subunits can form a stable dimeric complex referred to as the beta-gamma complex .[2]

 

Source:

 

G-proteïne

G-proteïne[1] (guanine nucleotide bindende eiwitten) of G-eiwit is een familie proteïnes betrokken bij de signaaloverdracht buiten de cel die veranderingen binnen de cel veroorzaakt. G-eiwitten zijn betrokken bij de signaaloverdracht van veel hormonen, neurotransmitters en andere signaalmoleculen.

Het G-proteïne bestaat uit twee delen, namelijk een α- en βγ-deel. Wanneer het G-proteïne inactief is bindt het α-deel met GDP. Het βγ-deel zit dan aan het α-deel vast. Als het G-proteïne actief is, is het gebonden met GTP en het α- en βγ-deel zijn van elkaar gesplitst. Het α-deel en/of βγ-deel kunnen dan reageren met een effector. Het G-proteïne werkt samen met de G-proteïnegekoppelde receptor (GPCR).

 

Source:

 

See also:

Project Rooftop

QDVM (Quantum Dot Vaccine Mark):

 

Bill Gates on Population Control

Source:

 

Bill Gates does want everyone vaccinated
And he just announced a new payment processing system associated with vaccines

 

Government Vaccination program:

Dutch National Immunisation Programme

 

THE BLACK ARMY

Dream / Vision of Dumitru Duduman

 

May 7th, 1993

One night, while in Oregon, I dreamed the sky was getting dark.  Then suddenly it turned pitch black!  It was as if the whole world had gone dark at that moment!   All the people were in a frenzy!  They became disoriented, and some were even screaming. After some time, we heard the sound of an army approaching.  Soon, we saw them coming out of the black mist.  All were dressed in black, except one.  That one seemed to be their leader.  He was dressed in a red robe with a thick black belt over his waist.  On his head, he had a sign.  As I looked, I saw that in his hand he held the same kind of sharp spear as everyone else in his army.

 

"I am Lucifer!" he exclaimed.  "I am the king of this world!  I have come to make war against the Christians!"

It looked as though all the Christians were huddled together in one big group.  Some began to cry when they heard this.  Others began to tremble, while some just stood without saying anything.  Lucifer continued to speak.  "All of those that want to fight against my army and think they can be victorious; go to the right.  Those that fear me; go to the left."

Only about a quarter of the group stepped to the right.  All the others went to the left.   Then Lucifer ordered his army, "Destroy those on the right!"

 

The army began to advance and quickly surrounded the Christians on the right.  As they began to close in on us, a powerful light appeared and encircled us.  Then, an angel of the Lord spoke.  "Take out your swords and fight.  Defend yourselves and be victorious over the enemy."

"What swords?" A man in the group asked.

"The Word of the Lord is your sword," the angel answered.  When we understood what the angel meant, we began to quote verses from the Bible.  Then suddenly, as if we were one voice, we began to sing a song.  Our voices thundered so loudly, that the Dark army began to retreat in fear.  They did not have the courage to come against us anymore.

 

Lucifer, then filled with rage, turned to those on the left.  "You, who all of your life have been trying to please two masters, because you could not stand against me; I have the power to destroy you."

He then ordered his army to attack.  It was a total massacre.  The ones on the left could not defend themselves.  One by one they all fell.  This killing seemed to go on for a long time.  After a while we could actually smell the stench of the dead.

 

"Why could they not be protected also?" someone asked.

The angel answered: "Because all their life they have been lukewarm.  Because of their hypocrisy, the true church has been blasphemed.  They have brought disrespect to the word of God.  They were not clean."

As we continued to look, we saw the sun coming over the horizon.  The black clouds began to break up.  Then they disappeared.  Only one was left - on which Lucifer and his army stood.   Lucifer looked at me shaking his fists and said, "I will destroy you even if I have to throw my spear at you from here!"  Then that cloud disappeared too.

 

As I looked around I began to see faces that I recognized among our group.  I saw a pastor from Bellflower - another from Indiana - one from Michigan - as well as many of my American friends.  This strengthened me greatly.  Then I awoke.  The first thought that came to my mind as I awoke was that this had been the last fight of the devil against the church.  If we remain faithful, we will be victorious.

 

Excepted from: 
Dreams and Visions From God
Copyright © 1994, 1996, 2000

 

Source:

 

Do not forget the times of Moses and the Manna and the Water and His protection.

 

Revelation 9:21; 21:8; 22:15; 17:5; 13
Nahum 3:4
Isaiah 74:4-13 (UN)

 

Source:

 

People believe in a virus you can NOT see.

But People do NOT believe in YHWH they can NOT see.

Who do you trust more Humans or God.

 

Ezekiel 18:

30 - “Therefore, you Israelites, I will judge each of you according to your own ways, declares the Sovereign Lord / the Lord GOD (אֲדֹנָי יְהוִה) Repent! Turn away from all your offenses; then sin will not be your downfall.

 

Exodus 10:

17 - Now forgive my sin once more and pray to YHWH your God to take this deadly plague away from me.”

 

Exodus 15:

26 - And said, If thou wilt diligently hearken to the voice of YHWH thy God, and wilt do that which is right in his sight, and wilt give ear to his commandments, and keep all his statutes, I will put none of these diseases upon thee, which I have brought upon the Egyptians: for I am YHWH that healeth thee.

 

James 5:
14 Is any sick among you? let him call for the elders of the church; and let them pray over him, anointing him with oil in the name of the Lord:
15 And the prayer of faith shall save the sick, and the Lord shall raise him up; and if he have committed sins, they shall be forgiven him.
16 Confess your faults one to another, and pray one for another, that ye may be healed. The effectual fervent prayer of a righteous man availeth much.

 

Exodus 15:

26 - And said, If thou wilt diligently hearken to the voice of YHWH thy God, and wilt do that which is right in his sight, and wilt give ear to his commandments, and keep all his statutes, I will put none of these diseases upon thee, which I have brought upon the Egyptians: for I am YHWH that healeth thee.

 

Matthew 24:

7 - For nation shall rise against nation, and kingdom against kingdom: and there shall be famines, and pestilences, and earthquakes, in divers places.

 

Luke 21:

11 - And great earthquakes shall be in divers places, and famines, and pestilences; and fearful sights and great signs shall there be from heaven.

 

Hosea 4:

1 - Hear the word of YHWH, ye children of Israel: for YHWH hath a controversy with the inhabitants of the land, because there is no truth, nor mercy, nor knowledge of God in the land.

2 - By swearing, and lying, and killing, and stealing, and committing adultery, they break out, and blood toucheth blood.

3 - Therefore shall the land mourn, and every one that dwelleth therein shall languish, with the beasts of the field, and with the fowls of heaven; yea, the fishes of the sea also shall be taken away.

6 - My people are destroyed for lack of knowledge: because thou hast rejected knowledge, I will also reject thee, that thou shalt be no priest to me: seeing thou hast forgotten the law of thy God, I will also forget thy children.

 

Psalm 91:

9 - Because thou hast made YHWH, which is my refuge, even the most High, thy habitation;

10 - There shall no evil befall thee, neither shall any plague come nigh thy dwelling.

11 - For he shall give his angels charge over thee, to keep thee in all thy ways.

 

Revelation 16:

2 - And the first went, and poured out his vial upon the earth; and there fell a noisome and grievous sore upon the men which had the mark of the beast, and upon them which worshipped his image.

8 - And the fourth angel poured out his vial upon the sun; and power was given unto him to scorch men with fire.

9 - And men were scorched with great heat, and blasphemed the name of God, which hath power over these plagues: and they repented not to give him glory.

10 - And the fifth angel poured out his vial upon the seat of the beast; and his kingdom was full of darkness; and they gnawed their tongues for pain,

11 - And blasphemed the God of heaven because of their pains and their sores, and repented not of their deeds.

 

 

 

The life is in the blood
Your body is the Temple of the Holy Spirit


Why do so many wish to defile Gods Temple with Sorceries and witchcraft

and refuse to repent of this?

ANTI means in the place of as well as against

 

Acts 11:8
Galatians 5:19-20
Revelation 9:21

 

Blood contains two main kinds of proteins: albumin and globulins. Blood proteins help your body produce substances it needs to function. These substances include hormones, enzymes and antibodies. Usually, the amount of total protein in your blood is relatively stable.

 

Albumin is made mainly in the liver. It helps keep the blood from leaking out of blood vessels. Albumin also helps carry some medicines and other substances through the blood and is important for tissue growth and healing. Globulin is made up of different proteins called alpha, beta, and gamma types.

 

Gamma globulins (one group of gamma globulins is the immunoglobulins, which are also known as "antibodies")

The immunologically active gamma globulins are also called "immunoglobulins" or "antibodies".

 

Human blood plasma levels: 

The normal concentration of globulins in human blood is about 2.6-4.6 g/dL.

 

Nonhuman globulins:
Globulin proteins exist not only in other animal species, but also in plants. Vicilin and legumin, from peas and other legumes, function as protein storage within seeds. These proteins can cause allergic reactions if they bind with human IgE antibodies.[1]

 

Jesus alone heals

(or not?)

 

New information on viral antigens could improve COVID-19 testing

 

 

Researchers in France and China have characterized antibody responses to a wide range of antigens present on severe acute respiratory syndrome-related coronavirus (SARS-CoV-2) among patients with coronavirus disease 2019 (COVID-19).

Novel Coronavirus SARS-CoV-2 Transmission electron micrograph of a SARS-CoV-2 virus particle, isolated from a patient. Image captured and color-enhanced at the NIAID Integrated Research Facility (IRF) in Fort Detrick, Maryland. Credit: NIAID

The team says that as well as improving the sensitivity and specificity of serology tests for early diagnosis of current infection, the findings could aid the identification of previous infection, which is essential for determining the rate of infection spread.

They could also lay the foundations for identifying which antigens should be prioritized as targets in vaccine development.

The team’s antibody assays showed that three antigens on the virus allow specific and sensitive detection of antibody responses early on in the infection.

“Our data reports the most extensive landscape of antibody responses of COVID-19 patients reported to date,” writes Sophie Valkenburg (School of Public Health, The University of Hong Kong) and colleagues. “We report, for the first time, the detection of antibody responses directed against an extensive spectrum of the SARS-CoV-2 antigens.”

A pre-print version of the paper is available in medRxiv*, while the article undergoes peer review.

 

Understanding more about viral antigens

The urgent need for a vaccine that will protect people against SARS-CoV-2 infection and mitigate the COVID-19 pandemic has led researchers to ask important questions about fundamental aspects of the immune response. In particular, they would like to know which viral antigens are responsible for triggering antibody responses and what this may imply about long-term protection.

The spike protein found on the surface of SARS-CoV-2 enables the virus to bind to host cells and is an important target in the development of diagnostic tests and vaccines.

Studies have shown that patients infected with SARS-CoV-2 develop a neutralizing response to the S1 subunit of the Spike protein, which contains the host-cell receptor binding domain. However, one recent study found that 10 of 175 infected patients did not develop this neutralizing response, yet ELISA assays still identified binding antibodies.

“These instances of low or no antibody responses by traditional serological approaches may lead to an underestimation of asymptomatic and mild infection and threaten the success of a potential vaccine that targets the S1 alone,” writes the team.

“Therefore, a broader landscape of antibody responses to a range of viral proteins needs to be assessed to better detect the immunogenicity of SARS-CoV-2 infection to improve the understanding of pathogenesis and immunity.”

 

Aside from the structural spike protein, the genome of SARS-CoV-2 also encodes for about 20 non-structural proteins.

The open reading frame (ORF) 1a/b encodes a large protein that is cleaved into 16 non-structural proteins (NSP1-16). Other ORFs may encode other proteins, but their functions are not known.

Now, Sophie Valkenburg and colleagues have used the Luciferase Immunoprecipitation System (LIPS) assay to compare antibody responses among infected versus uninfected individuals (controls) to 15 potential antigens on SARS-CoV2.

The antigens included four structural proteins (S, N, M, and E), the three spike protein subunits (S1, S2, S2’) seven ORFs (ORF3a, 3b, 6, 7a, 7b, 8 and 10) and one NSP within ORF1a/b (NSP1).

“The LIPS technique has previously been used to distinguish infected versus vaccinated cases for influenza due to the presence of antibodies against non-structural proteins, and to characterize human infections by zoonotic spillover from bat viruses,” explains the team.  

What did the study find?

The researchers identified significant between-group differences in the strength of responses to antigens S, S1, and S2’,  but these proteins did not demonstrate high sensitivity, especially in cases of early infection.

Of the eight ORFs, six induced antibody responses in infected patients, namely NSP1 (ORF1ab), ORF3a, ORF3b, ORF7a, ORF7b, and ORF8.

The researchers used cut-off values to calculate that three of these antigens - N, ORF3b, and ORF8 - were informative and sensitive enough to be used in diagnostic tests. When they combined these three antigens, they found they could correctly distinguish all infected patients from healthy controls with 100% sensitivity and specificity.  

What are the implications of the study?

Valkenburg and team say a test that combines several antigens other than the spike protein could provide useful extra information for identifying SARS-CoV-2 exposure and for avoiding false negatives.

“We found that the single test detection of N, S, or ORF3b antibodies at early time-points (day 4 to day 14) results in a high proportion of false-negative results, while the minimal combination of N+ORF3b+ORF8 LIPS tests is highly sensitive and specific.”

Importantly, notes the team, “ORF3b and ORF8 are the least identical proteins to SARS-CoV-2, and they do not exist in other strains of human coronaviruses.”

The researchers say the performance of their test needs to be confirmed and refined using more significant numbers of COVID-19 patients and uninfected controls.

They also say that they still need to explore whether antigens aside from spike provide protection.  

“Such information will help prioritize antigen targets for vaccine development, monoclonal antibody reagents and detecting early responses to infection,” conclude Valkenburg and the team.

*Important Notice

medRxiv publishes preliminary scientific reports that are not peer-reviewed and, therefore, not be regarded as conclusive, guide clinical practice/health-related behavior, or treated as established information.

Journal reference:

 

Source: 

 

An Introduction To Virology

Virology Lectures 2018 #5: Attachment and Entry

Source:

 

Vectors:

an organism, typically a biting insect or tick, that transmits a disease or parasite from one animal or plant to another.

 

Vector (biology)

Traditionally in medicine, a vector is an organism that does not cause disease itself but which spreads infection by conveying pathogens from one host to another.

Species of mosquito, for example, serve as vectors for the deadly disease Malaria.

This sense of "biological vector" is the primary one in epidemiology and in common speech.

In gene therapy, a virus itself may serve as a vector, if it has been re-engineered and is used to deliver a gene to its target cell.

A "vector" in this sense is a vehicle for delivering genetic material such as DNA to a cell.

 

Note:   The above text is excerpted from the Wikipedia article "Vector (biology)", which has been released under the GNU Free Documentation License.

 

Source:

 

pathogen

noun

MEDICINE
plural noun: pathogens
  1. a bacterium, virus, or other microorganism that can cause disease.

 

virus

noun
  1. 1.
    an infective agent that typically consists of a nucleic acid molecule in a protein coat, is too small to be seen by light microscopy, and is able to multiply only within the living cells of a host.
    "the hepatitis B virus"
     
     
  2. 2.
    a piece of code which is capable of copying itself and typically has a detrimental effect, such as corrupting the system or destroying data.

 

 

Vector (biologie)
Traditioneel in de geneeskunde is een vector een organisme dat zelf geen ziekte veroorzaakt, maar dat infectie verspreidt door pathogenen van de ene gastheer naar de andere over te brengen.

Zo dienen muggensoorten als vectoren voor de dodelijke ziekte Malaria.

Dit gevoel van "biologische vector" is het belangrijkste in de epidemiologie en in gewone spraak.

Bij gentherapie kan een virus zelf als vector dienen, als het opnieuw is ontworpen en wordt gebruikt om een gen af te leveren aan zijn doelcel.

Een "vector" in deze zin is een drager voor het afleveren van genetisch materiaal zoals DNA aan een cel.

 

Opmerking: de bovenstaande tekst is een uittreksel van het Wikipedia-artikel "Vector (biologie)", dat is vrijgegeven onder de GNU-licentie voor gratis documentatie.

 

Pathogeen

Ziekmaker

 

Definitie: 

Een pathogeen is een biologische ziekteverwekker, bijvoorbeeld een bacterie, virus of schimmel. Er wordt een onderscheid gemaakt tussen obligate pathogenen, die altijd een ziekte veroorzaken, en facultatieve pathogenen, die soms onschadelijk blijven.

 

Source:

 

Viruses are obligate intracellular parasites and must enter cells to replicate, but they are too big to simply pass through the cell membrane. In this lecture we discuss how icosahedral and enveloped viruses attach to cell receptors, how the virus particle is destabilized, allowing the nucleic acid to enter the cell, and how membrane fusion is regulated.

 

Virussen zijn obligate intracellulaire parasieten en moeten cellen binnendringen om zich te vermenigvuldigen, maar ze zijn te groot om gewoon door het celmembraan te gaan. In deze lezing bespreken we hoe icosahedrale en omhulde virussen zich hechten aan celreceptoren, hoe het virusdeeltje wordt gedestabiliseerd, waardoor het nucleïnezuur de cel kan binnendringen en hoe membraanfusie wordt gereguleerd.

 

How does a virus go into a cell?

  • Step 1: Adhere to cell surface (electrostatics)
    - No specificity
  • Step 2: Attach to specific receptor molecules on cell surface
    - More than one receptor may be involved
  • Step 3: Transfer genome inside the cell

 

Hoe komt een virus een cel binnen?

  • Stap 1: Hecht aan het celoppervlak (elektrostatica)
    - Geen specificiteit
  • Stap 2: Bevestig aan specifieke receptormoleculen op het celoppervlak
    - Er kan meer dan één receptor bij betrokken zijn
  • Stap 3: Breng het genoom over in de cel

A receptor That can be easily removed from cells using an enzyme called

 

Cellular receptors for viruses

  • Essential for all viruses except those of fungi (no extracellular phases) and plants (enter cells by mechanical damage)
  • 1985: once receptor known, sialic acid for influenza virus

 

Cellulaire receptoren voor virussen

  • Essentieel voor alle virussen behalve die van schimmels (geen extracellulaire fasen) en planten (dringen cellen binnen door mechanische schade)
  • 1985: één receptor bekend, siaalzuur voor influenzavirus

Een receptor die gemakkelijk uit cellen kan worden verwijderd met behulp van een enzym genaamd

 

receptor

 

noun

PHYSIOLOGY
  1. an organ or cell able to respond to light, heat, or other external stimulus and transmit a signal to a sensory nerve.
    "the retina of the octopus has up to 20 million light receptors"
     
  • a region of tissue, or a molecule in a cell membrane, which responds specifically to a particular neurotransmitter, hormone, antigen, or other substance.
"when viruses succeed in binding to cell membrane receptors they still have to enter the cell before they can replicate"

 

receptor

zelfstandig naamwoord

FYSIOLOGIE

  1.  een orgaan of cel die in staat is om te reageren op licht (Luciferace), warmte of andere externe prikkels en een signaal naar een sensorische zenuw te sturen.
    "het netvlies van de octopus heeft tot 20 miljoen lichtreceptoren"
  • een weefselgebied, of een molecuul in een celmembraan, dat specifiek reageert op een bepaalde neurotransmitter, hormoon, antigeen of andere stof.

"wanneer virussen erin slagen te binden aan celmembraanreceptoren, moeten ze de cel nog binnenkomen voordat ze kunnen repliceren"

 

For animals: We need a receptor to get into the cells
A receptor can easily removed from cells by using an enzyme called

 

Voor dieren: we hebben een receptor nodig om in de cellen te komen
Een receptor kan gemakkelijk uit cellen worden verwijderd met behulp van een enzym genaamd

 

Criteria for identifying cell receptors for viruses

Receptor binds virus particle
Antibody to recepter blocks infection
Receptor gene confers susceptibility
- More than one receptor may be involved
Disruption of receptor gene blocks infection

 

Criteria voor het identificeren van celreceptoren voor virussen

Receptor bindt virusdeeltje
Antilichaam tegen recepter blokkeert infectie
Receptorgen geven gevoeligheid
- Er kan meer dan één receptor bij betrokken zijn
Verstoring van receptorgen blokkeert infectie

 

We have a number of enabling technologies

  • If you identify a protein on the cellsurface that you think is your virus receptor
    obiously you have to show that it binds your virus
    so either on the cell surface or
    you can produce the protein by methods that you show that it will bind the virus particles
  • An other good way to demonstrate virus receptors specificities to make an antibody against the receptor protein and show that it blocks infection with the virus
  • And the 3th way you somehow get the GENE encoding the receptor

many ways you can do that
you then put it into cells that do NOT have the receptor
and then hopefully the GENE will be expressed the receptor will be put than on the surface

 

We hebben een aantal ondersteunende technologieën

  • Als u een eiwit op het celoppervlak identificeert waarvan u denkt dat het uw virusreceptor is
    Je moet natuurlijk aantonen dat het je virus bindt
    dus ofwel op het celoppervlak of
    je kunt het eiwit produceren door middel van methoden waarmee je aantoont dat het de virusdeeltjes zal binden
  • Een andere goede manier om de specificiteit van virusreceptoren aan te tonen om een antilichaam tegen het receptoreiwit te maken en te laten zien dat het infectie met het virus blokkeert
  • En de derde manier om op de een of andere manier het GEN te krijgen dat de receptor codeert

vele manieren waarop u dat kunt doen
je stopt het dan in cellen die de receptor NIET hebben
en dan hopelijk zal het GEN tot expressie komen, de receptor zal dan aan de oppervlakte worden gebracht

 

 

Normally, ACE2 is found on lung, kidney, heart, and gut cells. But scientists recently found ACE2 receptors on the cells in peoples’ noses — an “aha” moment for people like Farzen who had studied the 2003-era SARS virus.

 

The coronavirus sneaks into cells through a key receptor.

Could targeting it lead to a treatment?

 

Excerpt:

Normally, ACE2 is found on lung, kidney, heart, and gut cells. But scientists recently found ACE2 receptors on the cells in peoples’ noses — an “aha” moment for people like Farzen who had studied the 2003-era SARS virus.

 

Source: 

 

 

Zijn de Covid PCR-tests een heimelijke manier om mensen te infecteren of iets bij hen te implanteren?

DOOR  · 24 AUGUSTUS 2020

 

 

De Covid PCR-tests worden uitgevoerd met een 15 centimeter lang wattenstaafje, dat de neus in wordt geduwd tot helemaal achterin de neusholte. Waarom? Het wattenstaafje komt in aanraking met de zeer gevoelige cribriforme plaat, ook wel zeefbeen genoemd, die direct toegang biedt tot je hersenen. Zit er een bijbedoeling achter deze tests?

 

Auteur: Makia Freeman, vertaling: Willem Frederik Erné

 

De Covid PCR-tests die over de hele wereld worden uitgerold, ongeveer in lijn met het 1-3-30-plan (*) van de Rockefeller Foundation, vormen het belangrijkste aandachtspunt van de huidige fase van Operatie Coronavirus.

Hoe meer mensen worden getest des te meer positieve gevallen worden vastgelegd, hetgeen de brandstof is voor het officiële paniekverhaal en de angst in stand houdt, waardoor nog meer tirannie kan worden gerechtvaardigd.

Er zou echter nog iets meer aan de hand kunnen zijn.

We moeten ons afvragen of deze Covid-tests niet een sluwe manier zijn om toegang te verkrijgen tot het binnenste van ons lichaam, met name onze hersenen. De neuswattenstaafjes die worden gebruikt (nasofaryngeaal of orofaryngeaal) zijn ongelooflijk lang (15 centimeter) wat betekent dat ze helemaal tot achter in de neusholte reiken.
Bestaat er een medische reden waarom deze wattenstaafjes zo lang moeten zijn? De

Covid-tests in kwestie zijn PCR-tests. In andere artikelen heb ik besproken hoe gebrekkig en ongeschikt PCR-tests zijn. Zou het zo kunnen zijn dat deze Covid-tests heimelijk worden gebruikt om mensen te infecteren (met een middel dat ziekte veroorzaakt), het vaccin toe te dienen (waarvan ze beweren dat het nog in ontwikkeling is) of zelfs iets bij mensen te implanteren (met nanotechnologie, bijv. microchips)?

Mikken de Covid PCR-tests op toegang tot het zeefbeen?

In de menselijke anatomie is de cribriforme plaat een middellijnbotje dat belangrijk is zowel als onderdeel van het cranium als van de neus, en waardoorheen de reukzenuwen lopen die onze reuk transporteren. Het zeefbeen is een zeer teer en fragiel deel van het lichaam. Waarom wordt bij de Covid-test in hemelsnaam met een wattenstaafje tegen dit tere botje aan gepord? Zou dat kunnen zijn omdat de cribriforme plaat toegang tot de hersenen biedt?

 

Jim Stone zinspeelde hier onlangs op in een artikel genaamd The Coronavirus test is not credible and likely to be for clandestine brain access dat op deze website te vinden is. Een lang citaat uit dit artikel:

“Ze beweren dat het virus bij een hoog percentage mensen het zenuwstelsel ruïneert, waarbij blijvende neurologische problemen en hersenbeschadigingen optreden. Maar ik vraag me af of het virus dat doet of dat dit het gevolg is van de tests. Beste mensen, het is overduidelijk dat de coronavirustests zelf in veel gevallen (er bestaan waarschijnlijk verschillende soorten tests) de hersenschade veroorzaken.

Een grove zeef

Eenvoudig gezegd: veel van de tests (ze gebruiken allemaal dat ongelooflijk lange wattenstaafje) halen het monster van de cribriforme plaat af, een botje van een millimeter dikte boven in de neusholte, dat is geperforeerd met veel gaatjes die direct toegang geven tot de hersencaviteit.

Door deze talrijke gaatjes lopen de reukzenuwen. Het botje lijkt op een grove zeef. Als je iemand te grazen zou willen nemen door stiekem een hersenvirus of een chip te implanteren, dan is dit de perfecte plek om dat te doen omdat een arts een chip er misschien nog uit zou kunnen halen, maar dat zou jou zelf nooit lukken zonder dat zeer dunne botje (dat eigenlijk niet eens een botje is maar voor de helft uit zenuwen bestaat) perforeren.

Iemand die zelf zou proberen iets daaruit te verwijderen zou zichzelf waarschijnlijk om het leven brengen. Alle chemicaliën, virussen – nanotechnologisch of anderszins – die men zou willen inbrengen, komen rechtstreeks in de hersenen terecht en die krijg je er nooit meer uit: eenmaal binnen, altijd binnen. Wanneer eenmaal ingebracht, gaat het rechtstreeks de hersenen in.

Waarom een pijnlijke test?

Mensen die de test ondergaan, klagen dat hij ongelooflijk pijnlijk is en dat de pijn dagenlang aanhoudt. Waarom moet de test uitgerekend dat deel van het menselijk lichaam aanraken dat het dichtst bij de hersenen zit? En zijn die tests eigenlijk wel tests?

DNA-test worden uitgevoerd met een simpel wattenstaafje in de mond en het is absurd om te denken dat welke virustest dan ook niet op dezelfde manier zou kunnen plaatsvinden, zeker als je bedenkt dat het virus door hoesten verspreid zou kunnen worden.

Iets deugt niet aan deze tests. Ze MOETEN wel nep zijn (in ieder geval die tests die letterlijk een monster van de hersenen nemen). Geen wonder dat zo’n test dagenlang pijn doet en jemig, als je reukzenuwen worden geraakt door wat zich ook op dat wattenstaafje moge bevinden, dan is DAT waarschijnlijk wat ervoor zorgt dat mensen hun reuk permanent verliezen.

Ik durf te wedden dat je niet wist hoe akelig deze test eigenlijk is. Onderwerp je onder geen beding aan deze test.
Oké, ik heb dat artikel een paar dagen geleden bekeken en er toen verder geen aandacht aan geschonken. Ik kon gewoon niet bevatten dat deze monsters hun barbaarse PCR-test zouden gebruiken als manier om onze hersenen te BESCHADIGEN! Nog los van de ethiek ervan kon ik me niet voorstellen dat deze smeerlappen zo verschrikkelijk diep zouden kunnen zinken. Maar nogmaals, we hebben te maken met monsters zonder menselijk geweten, weet je nog?”

Veroorzaakt de Covid PCR-test fysieke schade?

Hier is nog een citaat van dezelfde website, maar niet van Jim Stone:

“(..) ze voerden de ‘tests’ uit door een maar liefst 15 centimeter lang wattenstaafje in ELK neusgat te steken, helemaal tot achterin de nasale doorgang. Vervolgens draaide de afnemer van de test het wattenstaafje gedurende 10 tot 15 seconden in elk neusgat rond… Daarna verwijderde hij de wattenstaafjes en stak ze in een testbuisje om naar het laboratorium te worden verzonden voor ‘analyse’…

Daar moest ik toch wel even over nadenken. Waarom was het in hemelsnaam nodig om zo’n lang wattenstaafje überhaupt helemaal tot achterin de nasale doorgang te steken? En vervolgens elk wattenstaafje tegen het zachte weefsel van dat plaatje achter in de nasale doorgang heen en weer te draaien? Dat leek me behoorlijk wreed! Zou die beweging alleen al dat plaatje kunnen beschadigen en mogelijk VEEL meer schade veroorzaken dan dit ‘virus’?

En iedereen met wie ik sprak vertelde hetzelfde verhaal, namelijk dat ze hoofdpijn kregen en in sommige gevallen misselijk werden en daarna ernstige voorhoofdsholtepijn hadden. Ik ben een chronische voorhoofdsholtehoofdpijnlijder en heb regelmatig dergelijke pijn achterin mijn neusholte, en ik weet dus wat ze doormaken. En dit alles wordt gedaan om met een ‘monster’ van het RNA van dit zogenaamde virus te verifiëren dat iemand positief is?

Nogmaals, het lijkt mij nogal wreed. Ik denk dat er veel eenvoudiger manieren zijn om weefselmonsters te krijgen dan door mogelijk schade te veroorzaken achterin de neusholte.”

Clandestiene methode

Er is iets uitermate verdachts aan deze Covid-tests. Laten we vooral niet vergeten dat bepaalde partijen van deze Covid-tests vervuild waren, soms met het coronavirus zelf (onder andere in de VS en het VK) – alhoewel fact checkers beweren dat dit ‘virus’ zich nie kon verspreiden en geen mensen kon infecteren, alleen de testresultaten ongeldig maakte.

Gezien het doel van de NWO (de nieuwe wereldorde) om de hele bevolking van microchips te voorzien, acht ik de samenzweerders van de NWO ertoe in staat dat ze een dergelijke afschuwelijke, clandestiene methode gebruiken om mensen, zonder dat ze het weten, met iets te implanteren, onder het mom van hulpverlening.

Ook het laserpistool is verdacht

Nog een vraag, nu we het toch over invasieve medische interventies hebben: verzwakt een laserpistool dat tegen je hoofd wordt gezet de pijnappelklier? Hoe zit het met die laserpistolen die je temperatuur meten? Je kunt de pech hebben dat je in een gebied woont waar bedrijven een laserpistool op je voorhoofd richten om je temperatuur te meten. Nog los van de medische consequenties, is dit overduidelijk een smakeloze manier van conditionering om mensen eraan te laten wennen dat ze een pistool tegen hun hoofd gezet krijgen.

Denk even na over wat we allemaal accepteren als we dit nieuwe normaal toestaan, waarbij pistoolachtige apparaten routinematig tegen ons hoofd worden gezet. Denk je in wat voor ongelooflijke schade we onze kinderen berokkenen als we toestaan dat zij aan dit soort praktijken gewend raken.

In deze interessante video wordt besproken hoe de infrarode straal van het pistool mogelijkerwijs je pijnappelklier beschadigt, het doorgangsportaal naar hogere energiesferen en bewustzijn. De man in de video citeert een Australische verpleegster:
“Ik maak me echt zorgen. Worden we gedesensibiliseerd ten aanzien van op het hoofd gerichte acties, waarbij mogelijk de gezondheid te lijden heeft ten gevolge van een infrarode straal die op de pijnappelklier wordt gericht?

Niet op de pijnappelklier richten

Ik ging naar een winkelcentrum waar de mensen in de rij stonden om hun temperatuur te laten meten door een medewerker die overduidelijk geen gezondheidszorgmedewerker was en overduidelijk niet goed wist hoe hij deze procedure moest uitvoeren. Veel omstanders waren stomverbaasd toen het mijn beurt was, ik het pistool dat op mijn hoofd werd gericht beetpakte en het op mijn pols richtte.

Ik vertelde de medewerker zacht maar zeer vastberaden dat je een infraroodthermometer nooit op iemands voorhoofd moet richten en al helemaal niet op dat van baby’s en jonge kinderen.

Bovendien moet je beschikken over basale kennis over hoe je iemands temperatuur goed afleest. Bijvoorbeeld, een thermometer op de pols of de binnenplooi van de elleboog plaatsen is veel nauwkeuriger en veel minder schadelijk. Ik vond het schokkend om te moeten zien hoe kinderen gewend raakten aan het feit dat een object in de vorm van een pistool op hun voorhoofd werd gericht, en wel zonder enige negatieve reactie van de volwassenen, alsof het de normaalste zaak van de wereld was.

Als medische professional weiger ik om een infrarode straal recht op de pijnappelklier te richten. Deze bevindt zich precies in het midden van het voorhoofd. Niettemin vinden de meeste mensen het prima dat dit bij hen diverse keren per dag gebeurt! Onze pijnappelklier moet beschermd worden omdat deze essentieel is voor onze gezondheid, nu en in de toekomst.

Thermale weefselbeschadiging

Een standaard infraroodthermometer absorbeert het infrarode licht maar zendt het niet uit. Vanuit dat perspectief zijn ze dus veilig. Het veiligheidsprobleem ontstaat bij laserthermometers, die een lichtbundel richten op het gedeelte van het object dat wordt gemeten, ter vergroting van de nauwkeurigheid. Deze bundel is een Klasse-II-laser die zichtbaar licht uitzendt van minder dan één milliwatt. Zo’n apparaat mag worden verkocht als ‘aanwijzer’ om aandacht te vestigen op smartboards of whiteboards bij lezingen.

Hoewel ze in principe als veilig zijn geclassificeerd, kunnen ze je netvlies beschadigen als je recht in de straal kijkt. Lasers produceren een intense lichtbundel die laserstraling kan veroorzaken in de vorm van thermale weefselbeschadiging. Hoe dichter je bij de laser bent, des te groter de kans om gewond te raken.”

Tot slot

Het doel van deze post is om bewustzijn te verhogen en vragen te stellen. Dit artikel geeft geen antwoorden op de vraag wat werkelijk in deze Covid-tests zit en of ze ontworpen zijn met een bijbedoeling. Hopelijk leiden deze eerste vragen tot verder onderzoek door andere mensen en moedigt het mensen in ieder geval aan om buitengewoon terughoudend te zijn ten aanzien van het zonder meer ondergaan van deze tests. Het moet nu toch wel duidelijk zijn dat niets aan Operatie Coronavirus goedaardig is, zelfs de tests niet.

Ieder aspect van deze agenda moet zorgvuldig onder de loep worden genomen. De test ondergaan is stilzwijgende instemming met het feit dat de test werkt en noodzakelijk is voor de volksgezondheid en veiligheid, hetgeen in beide gevallen volstrekt onwaar is.

(*) Van 1 miljoen tests per week naar 3 miljoen per week en uiteindelijk 30 miljoen per week (in de VS)

Bronartikel

Gerelateerd

De coronatest is niet alleen onzinnig, maar mogelijk ook gevaarlijk

 

Source: 

 

 

Revelation 14:

And the third angel followed them, saying with a loud voice, If any man worship the beast and his image, and receive his mark in his forehead, or in his hand,

 

A surgical mask protects patients against bacteria, it does NOT protect you against a virus.

 

Source:

 

Definition Virus: A microorganism that is smaller than a bacterium that CANNOT GROW or REPRODUCE apart from a living cell. A virus invades living cells and uses their chemical machinery to keep itself alive and to replicate itself.

 

So you have to be injected by it. A virus is not a living organism.

 

What are Germs:

Germs are tiny animals which are so small they cannot be seen without the help of a special instrument called a microscope. The microscope allows the germs to be seen by making them look a lot bigger. Many of these germs will cause disease in humans and other animals.

 

There are two main types of germs which can cause disease in humans and animals. These are bacteria and viruses. Bacteria are larger than viruses.

 

Diseases caused by bacteria germs are called bacterial diseases, and those caused by virus germs are called viral diseases.

 

Bacteria germs can get into sores, cuts and broken skin and into the ears and cause pus sores. These germs can be of many different types, but not all the germs that reach these places will cause infection.

 

Germs can get into cuts, sores and broken skin when these places come into direct contact with things which have the germs on them, such as:

hands

soil

pets

flies and other insects

faeces

 

The spread of germs

Germs live anywhere they can find warmth, food and moisture. This could be:

inside people's bodies or on their skin

inside or on the bodies of other animals

in sewage systems

on food

on rubbish of any kind

on the ground

in unclean water

in the air

 

WATER is a colourless, transparent, odourless liquid that forms the seas, lakes, rivers, and rain and is the basis of the fluids of living organisms.

 

 

Viruses are not living things. Viruses are complicated assemblies of molecules, including proteins, nucleic acids, lipids, and carbohydrates, but on their own they can do nothing until they enter a living cell. Without cells, viruses would not be able to multiply. Therefore, viruses are not living things.

 

A virus consists of nucleic acids (DNA or RNA) ENCLOSED in a PROTEIN COAT that may also shelter viral proteins involved in infection. By that description, a virus seems more like a chemistry set than an organism. But when a virus enters a cell (called a host after infection), it is far from inactive. It sheds its coat, bares its genes and induces the cell’s own replication machinery to reproduce the intruder’s DNA or RNA and manufacture more viral protein based on the instructions in the viral nucleic acid. The newly created viral bits assemble and, voilà, more virus arises, which also may infect other cells.

 

They want to inject you with the VACCINE (POISON/MEDICATION/FARMACIA/ PHARMACY) so the VIRUS can be injected and change your DNA/RNA your SUBSTANCES = PROTEINS. (They have to enter your Proteins to change your DNA....they call it to KILL the GOD GENE.

Look up the word LAMININ in google and SUBSTANCES in the Black's Law book 7th EDITION. There is a juriprudence about these SUBSTANCES.

 


LAMININ (Looks like a CROSS) are high-molecular weight (~400 to ~900 kDa) proteins of the extracellular matrix. They are a major component of the basal lamina (one of the layers of the basement membrane), a protein network foundation for most cells and organs. The laminins are an important and biologically active part of the basal lamina, influencing cell differentiation, migration, and adhesion.

 

"So far as legal theory is concerned,
a person is any being
whom the law regards as capable of rights and duties.
Any being that is so capable is so person,
whether a human being or not,
and no being that is not a capable
is a person even though he be a man.
Persons are the substances of which rights and duties are.
The juridical significance,
and this is the exclusive just of view
from which personality receives legal recognition.

John Salmond, Jurisprudence 318 (Glanville L. Williams ed. 10th ed. 1947)

 

Hebrews 11:

1 Now FAITH is the SUBSTANCE of things hoped for, the evidence of things not seen.

2 For by it the elders obtained a good report.

3 Through faith we understand that the worlds were framed by the word of God, so that things which are seen were not made of things which do appear.

 

James 2:
9 But if ye have respect to PERSONS, ye commit SIN, and are convinced of the law as transgressors.
10 For whosoever shall keep the whole law, and yet offend in one point, he is guilty of all.
11 For he that said, Do not commit adultery, said also, Do not kill. Now if thou commit no adultery, yet if thou kill, thou art become a transgressor of the law.

 

Deuteronomy 1:
17 Ye shall not respect PERSONS in judgment; but ye shall hear the small as well as the great; ye shall not be afraid of THE FACE OF MAN; for the judgment is God's: and the cause that is too hard for you, bring it unto me, and I will hear it.

 

Vaccine (noun)
- a substance used to stimulate the production of antibodies and provide immunity against one or several diseases, prepared from the causative agent of a disease, its products, or a synthetic substitute, treated to act as an antigen without inducing the disease.


"THERE IS NO VACCINE AGAINST THE VIRUS"???????

(source is google search) Verry strange thing written in the definition?

 

- a substance containing a virus or bacterium in a form that is not harmful, given to a person or animal to prevent them from getting the disease that the virus or bacterium causes:
This vaccine protects against some kinds of the bacteria.

 

- a special substance that you take into your body to prevent a disease, and that contains a weakened or dead form of the disease-causing organism
Source:

 

Foreign substance

A substance found in a body, organism, or thing where it is not supposed to be found

<the plaintiff sued because she thought she saw - and later confirmed that she had found - a foreign subs

 

Celeste Solum

"Have We Entered The Golden Age? BioLogos, NanoSlaughterbots & More" - 10/14/20

Source:

 

FOR MORE GREAT VIDEOS, PLEASE JOIN CELESTE'S NEW VIDEO PLATFORM:

 

The Key

 

Standing Civilian Army

 

Golden Age (Satanic)

 

CIA Briefing

 

Excerpt:

New Fluorescent Substrate Enables Quantitative and High-Throughput Examination of Vesicular Monoamine Transporter 2 (VMAT2)

 

Considering the continuing interest in VMAT2 as a drug target, as well as a target for the design of imaging probes, we have developed a fluorescent substrate well suited for the study of VMAT2 in cell culture. Herein, we report the synthesis and characterization of a new fluorescent probe, FFN206, as an excellent VMAT2 substrate capable of detecting VMAT2 activity in intact cells using fluorescence microscopy, with subcellular localization to VMAT2-expressing acidic compartments without apparent labeling of other organelles. VMAT2 activity can also be measured via microplate reader.

 

Source: 

 

Excerpt:

Synthesis and Discovery of Arylpiperidinylquinazolines: New Inhibitors of the Vesicular Monoamine Transporter

 

Methamphetamine, a human vesicular monoamine transporter 2 (VMAT2) substrate, releases dopamine, serotonin, and norepinephrine from vesicles into the cytosol of presynaptic neurons and induces reverse transport by the monoamine transporters to increase extracellular neurotransmitters.

 

(APQs) are potent inhibitors of reserpine binding at recombinant human VMAT2

 

These compounds are bio-diaster-eo-selective and bio-enantio-selective (opposite or mirrored life selective).

 

Novel APQ ligands have high potency and may be useful tools for characterizing drug-induced effects on human VMAT2 expression and function.

 

Source:

 

Mad Scientists

 

Techne Logos

 

Excerpt:

This is an essentail to watch two-part conversation on neurotechnology. We certainly need to keep of finger on the pulse of Neurocognitive Enhancement. As you will discover it spans the molecular level to ethical, moral, theological, and spirituality issues at the scalar level. The neuro-technology field is a global enterprise.

 

 

This discussion tackles the tough questions about:

  • Construct of Consent
  • Ethics of Indwelling Devices (Yes, you heard correctly, indwelling devices hydrogel anyone?)
  • Palette of techniques and technologies that can be directed to neurological nodes (technical speak for you)
  • Brain Computer Interface
  • Networking with Indwelling Brain Entities
  • Yoking of human and machine
  • Engineering and devices that are programmable and that are direct about and that are also communicable at a level that is actually smaller than a cell allows us to create vast arrays of material that may be indwelling within the brain other systems that then allow us to work from the very small scale of the subcellular to the very large scale of the multi-dimensional
  • Interconnectivity that allows both communication in some cases articulation
  • Predictive Crime
  • Radical novel leveling
  • Continuity of Enhanced and Post-Enhanced Care
  • Techne Logos the Technical Word (vs God's Word)

 

Where is the mind (and soul) in the brain)? How far should we go? What should be do is contentious. What are the implications? Do we have cognitive liberty?

 

This technology ushers in:

  • A Teche Logos (word) that usurps God's Word
  • A counterfeit Indwelling Entity(ies) (A counterfeit Holy Spirit)
  • Synthetic Spiritual Yolking

All that is needed is for the Anti-Christ to be revealed.

 

BioLogos

 

 

Is there a scientific path to god?  (Which GOD!!!)

 

History

 

“Tonight, I'm launching a new Precision Medicine Initiative to bring us closer to curing diseases like cancer and diabetes — and to give all of us access to the personalized information we need to keep ourselves and our families healthier.”

President Barack Obama, State of the Union Address, January 20, 2015

(It's health care tailored to you.)

 

Source: 

 

FACT SHEET: Obama Administration Announces Key Actions to Accelerate Precision Medicine Initiative

 

Doctors have always recognized that every patient is unique, and doctors have always tried to tailor their treatments as best they can to individuals. You can match a blood transfusion to a blood type — that was an important discovery. What if matching a cancer cure to our genetic code was just as easy, just as standard? What if figuring out the right dose of medicine was as simple as taking our temperature?

President Obama, January 30, 2015

 

Source: 

 

HDIAC

 

DARPA

 

Structure-Guided Drug Design Could Yield Fast-Acting Remedies for Complex Neuropsychiatric Conditions


Slowing Biological Time to Extend the Golden Hour for Lifesaving Treatment


Biostasis

 

BioStasis What is biostasis?

 

Biostasis

Dr. Tristan McClure-Begley

 

The Biostasis program aims to extend the time for lifesaving medical treatment, often referred to as “the Golden Hour,” following traumatic injury or acute infection, thus increasing survivability for military personnel operating in far-forward conditions with limited access to medical professionals or trauma centers. To do so, Biostasis is developing novel chemical biology approaches that reversibly and controllably slow biological systems without cold-chain to stabilize and protect their functional capacity until medical intervention is possible.

Biostasis is investigating novel applications of polymer chemistry, protein engineering, and deep cell activity monitoring to alter the time course of pathological processes associated with tissue damage and infection to delay the onset of irreversible damage. Researchers are investigating approaches that are not dependent upon reducing temperature and that scale from preservation of simple biological therapeutics such as antibodies and enzymes to whole cells and tissues.

The program seeks to generate proof-of-concept, benchtop technologies and experimentally validate them in simple biological systems. DARPA will work with federal health and regulatory agencies as the program advances to develop a pathway for potential, future human medical use of successful Biostasis technologies. By the end of the program, DARPA hopes to have multiple tools for reducing the risk of permanent damage or death following acute injury or infection. Biostasis technologies could also extend the shelf-life of temperature-sensitive therapeutics, such as blood products, enzyme preparations, and drugs.

 

Focused Pharma

 

Excerpt:

Military service members experience an increased lifetime risk of neuropsychiatric conditions, such as depression, post-traumatic stress, and substance abuse.

 

Dr. Amy Jenkins

 

Excerpt:

She contributed to development of programs targeting infectious disease threats within Biological Technologies Office (BTO).

She also served as a National Research Council postdoctoral fellow at the U.S. Army Medical Research Institute of Infectious Diseases, where she studied virulence mechanisms of biodefense pathogens.

 

Articles & Blog

 

Video & Audio Production:

 

#neuroweapons #nano #celeste:

 

CCDC CBC-TR-1599, Cyborg Soldier 2050:

Human/Machine Fusion and the Implications for the Future of the DOD

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