Vmedvil

Well, Electron on positron collisions create Gamma radiation, Proton on Anti proton create gamma rays and High Energy Proton- anti proton many particles, High Energy Proton on Proton many particles from their energy mass, So High energy Electron on Electron should create many particles from their energy mass like proton on proton through Tachyon Condensation of the Higgs Field. Low Energy Edit: ya, see I thought that looked wrong, I thought it was 6 photons not 10 photons for low energy Proton-Antiproton, but I knew the electron-positron was right so I trusted it. Refer to sensei's Post after this one for low energy Proton-Antiproton. High Energy Matter/Antimatter collider High Energy Matter/Matter collider So, basically at high energies collisons cause most of the Energy to be dumped into Rest mass. So Muons or Tauons as a result even in electron on electron depending on what energy is actually required to break the symmetry of electrons higher would be Tauons, lower Muons.

You would die from massive internal bleeding in seconds to hours depending on the level of damage to the Aorta or spleen. Head trauma with internal bleeding (intracranial hemorrhage) Bleeding around the lungs (hemothorax) Bleeding around the heart (hemopericardium and cardiac tamponade) Tears in the large blood vessels near the center of the body (aorta, superior and inferior vena cava, and their major branches) Damage caused by trauma to the abdomen such as liver or spleen lacerations or perforation of other organs

So, people know what it says (==== (Nuclei Vibration and Molecular Coupling Hamiltonian Energy Stress =================================)(============= ∇'(x,y,z,t,ωs,ωp,M,I,k,φ,S,X,Z,μ,Y,q,a,β) = (((ħ2 /(2Erest/C2)) ∑3a =1 (d2/d((C2/Erest)∑Ni = 1 MiRi)2) + (1/2)∑3a,β = 1 μaβ(Pa - Πa)(Pβ - Πβ) + U - (ħ2/2)∑3N-6s=1(d2/dq2) + V)((|(Log(DgDaDψDφ-W) ====Maxwell Electromagnetism=Dirac========= QE Virtual Ghost particles======= Hypercharged Higgs===========Particle Coupling======Standard Higgs== (((2ħGC2))Rs - (1/4)FaμvFaμv + i(ψ-bar)γμ(((Lghost QE - gfabc(δμ (c-bar)a)Aμbcc) / (c-bar)aδμca) + ig(1/2)τWμ + ig'(1/2)YBμ)ψi +(ψ-bar)iLVijφψjr + (aji) - (μ2((φ-Dagger)φ) + λ((φ- ============= Virtual Particles Gravity =================== and Hypercharged Higgs=Spin Q Number=)(== Energy Stress Tensor Rest Mass and Rest Energy Dagger)φ)2)/-(((Lghost QE - gfabc(δμ (c-bar)a)Aμbcc) / (c-bar)aδμca) + ig(1/2)τWμ + ig'(1/2)YBμ)2)|)-e2S(r,t)/h)) - ((Erest/C2)ωs((((8πGTab/C4) + Λgab - Rab) * gab-1))1/2 + =Angular precession of moving Rest Mass and Rest Energy================Quantum Action of it)(=================Energy Stress angular momentum== (S/ (((3G(Erest/C2))/2C2Rs3)(RpVp) + (GIs/C2Rs3)((3Rp/Rs2)(ωp Rp) -ωp ))))Rs2/2))) / (ħ2/2(Erest/C2))))1/2(((1-(((2(Erest/C2)G / Rs) - (Isωs((((8πGTab/C4) + Λgab - Rab) * gab-1))1/2 + Angular Precession of Angular momentum================================) (==========Energy Stress of Linear momentum== Energy Stress of Strong (S/(((3G(Erest/C2))/2C2Rs3)(RpVp) + (GIs/C2Rs3)((3Rp/Rs2)(ωp Rp) -ωp )))))/2(Erest/C2))+ (((8πG/3)((g/(2π)3)∫(((Erelativistic2 - Erest2 / C2) + ((Ar(X) + (ENucleon binding SNF ε0 μ0 /mu) - Interaction and electron orbitals= Energy Stress of Temperature= Energy Stress of Particle Annihilation===Inverse Stress of Dark Energy=======) Ar(XZ±)/Z) / mu)2)(1/2)(1/e((ERelativistic - μchemical)/TMatter)±1)(ħωs + ħωs) - ((ksC2)/ Rs2) + (((8πGTab/C4) + Λgab - Rab) * gab-1))1/2(ΔKiloparsec)))2/(C2)))1/2)

New Structure added for Iron and Copper chemical binding. Nanoparticles won't defeat this virus, these added proteins protect the action of Standard integrase and Standard Reverse trancriptase from nano-particle disruption. . Nanoparticle https://newatlas.com/nanoparticle-antiviral-virus/52667/ The Encryption brute force strength is 1,099,511,627,776 or 420 attempts of the activation key Guide RNA. Which currently would take 34,865.285000507356671740233384069 years to crack via brute force method to activate successfully without misfolds in the proteins that make them nonfunctional.

Crispr Cleavage sites needed which needs to cleave at the same site as p10 "CCC or GGG" " p10 Cleavage site" NNNN, N=20 - Np10 Cleavage site which will now go through DNA and Protein segmentation which grooms the protein site, so the protein will still fold correctly which p10 cleavage instead of its natural Cleavage protein which does protolysis on it. Which the Viral Targetting and lethality will be activated when the CRISPR Guide RNA sequence for the cleavage command enters a cell infected with it, which is a Key to activation otherwise it will sit dormant inside a cell like HIV before AIDS, which is complete stealth to the immune system, via IL-10 , IL-35 and HIV-1 Capsid/ENV. They will think it is a white blood cell, like a Cytotoxic T-Cell when in reality it is a Synthetic Virus. The T-helper cells will recognize it as a Cytotoxic T-Cell despite having viral glycoprotiens. The Immune system will kill any foreign object attacking this Virus as if it were under attack creating a huge immune response to attempts in removal after integration into a genome. Any Biochemistry using Copper or Iron will be subject to cleaveage through Hydrolysis and ionization of their proteins through action Synthetic Metal Binding Intgrase P32 which will be added.

Next the p10 protease Cleavage sites need to be added.

Next, will be CRISPR Guide RNAs for Cas9 to silencing of genes that pose a threat to the pathogen's stability as adaptive defensive Gene Disruption. Which just requires a Primer then Target sequence.

That is one part of what was unbanned only part. In any case, Measles, SARS, and Hepatitis C, HIV-1, and Rabies are present on MV-5 being Skin,Lung, Liver, T-cell, and Nerve cells infectivity on mammals. The New Version, with defensive mechanics along with innate and adaptive Immune system disabling abilities.

I know, I was just saying that is what it is closest to, which cannot be what caused it as it is man-made process, Protoplast fusion.

In any case, when used with a Immune suppressor there is no doubt that Sanguinarine would act like Organic Agent VX, VX acts on Acethycholine transfer (chemical messagers) in nerves and not Electrical potential causing Pumps in nerves but both should be equally effective. Nerve agent VX US army test Deadliest Weapon VX History Channel while Cheilanthifoline like the Cytotoxicity effects of Ebola or Marburgs virus. making them perfect genes for this purpose.

Well, since bacteria were here first, I assume that, the thing that Meiosis I is actually closest to is Protoplast fusion in synthetic biology. But that is a unnatural processes created by man, protoplast fusion.

No i don't care about the funding it is a different part of it the Federal Ban was lifted on deadly pathogen research and creation. Which extends to my Gene Therapy Vector designs which can be transformed into Deadly Pathogens, by reintroducing self replication. legally now. Self Replicating (Extremely Lethal) BSL-4 Does not reproduce (Harmless) BSL-0

Close enough if the NIH has resumed their research into the deadly aspects of Bio-engineering and reversed the federal ban, which nullifies Nixon's end to it. The effects of Cheilanthifoline on mammals. Activity Activity Value [µM] Substance SID BioAssay AID BioAssay Name Target Active 20.63 104237812 493705 Cytotoxicity against human A549 cells by SRB assay Active 27.41 104237812 493706 Cytotoxicity against human SKOV3 cells by SRB assay Active 22.24 104237812 493707 Cytotoxicity against human SK-MEL-2 cells by SRB assay Active 29.84 104237812 493708 Cytotoxicity against human HCT15 cells by SRB assay and Sanguinarine is a toxin that kills animal cells through its action on the Na+/K+-ATPase transmembrane protein. And I had it reversed it had been a minute, Sanguinarine is the neurotoxin and Cheilanthifoline is the Cytotoxicity and Necrosis.

I think I said that too. that Plasmid exchange does not cause production but gene transfer. https://sciencesamhita.com/what-is-bacterial-conjugation/ http://www.pagepress.org/journals/index.php/eb/article/view/eb.2012.e1/6012 Which I would say evolved from a Gene Transfer method to a reproduction mode in plants around 1.3 to 1 Billion years ago branching into fungi and so on.

Third Article Third article about this.

The Purpose of this is to Design Metamorphic Viral Pathogens named after the Synthetic Pathogens for Star Trek Deep Space Nine meaning of Metamorphic in coding Metamorphic Code The Beginning of this will start with this. Here was a Earlier creation the MV-5 Zombie Virus, which is Polymorphic Polymorphic Code In 1969, President Richard Nixon ended all offensive (i.e., non-defensive) aspects of the U.S. bio-weapons program. In 1975 the U.S. ratified both the 1925 Geneva Protocol and the 1972 Biological Weapons Convention (BWC)—international treaties outlawing biological warfare, which has been repealed making this legal. Genetic warfare Theoretically, novel approaches in biotechnology, such as synthetic biology could be used in the future to design novel types of biological warfare agents.Special attention has to be laid on future experiments (of concern) that: Would demonstrate how to render a vaccine ineffective; Would confer resistance to therapeutically useful antibiotics or antiviral agents; Would enhance the virulence of a pathogen or render a nonpathogen virulent; Would increase transmissibility of a pathogen; Would alter the host range of a pathogen; Would enable the evasion of diagnostic/detection tools; Would enable the weaponization of a biological agent or toxin Start Two Interesting add genes would be Organic Neurotoxin Synthase Cheilanthifoline or Necrosis Synthase Sanguinarine and Possibly Strong Immuno Supressor IL-10 or Weak Immuno Suppressor IL-35.

Article Article about this. Second Article Second article about this.

Oh, I wanted to post this before someone reads this far into the post as my final change. ∇'(x,y,z,t,ωs,ωp,M,I,k,φ,S,X,Z,μ,Y,q,a,β) = (((ħ2 /(2Erest/C2)) ∑3a =1 (d2/d((C2/Erest)∑Ni = 1 MiRi)2) + (1/2)∑3a,β = 1 μaβ(Pa - Πa)(Pβ - Πβ) + U - (ħ2/2)∑3N-6s=1(d2/dq2) + V)((|(Log(DgDaDψDφ-W)(((2ħGC2))Rs - (1/4)FaμvFaμv + i(ψ-bar)γμ(((Lghost QE - gfabc(δμ (c-bar)a)Aμbcc) / (c-bar)aδμca) + ig(1/2)τWμ + ig'(1/2)YBμ)ψi +(ψ-bar)iLVijφψjr + (aji) - (μ2((φ-Dagger)φ) + λ((φ-Dagger)φ)2)/-(((Lghost QE - gfabc(δμ (c-bar)a)Aμbcc) / (c-bar)aδμca) + ig(1/2)τWμ + ig'(1/2)YBμ)2)|)-e2S(r,t)/h)) - ((Erest/C2)ωs((((8πGTab/C4) + Λgab - Rab) * gab-1))1/2 + (S/ (((3G(Erest/C2))/2C2Rs3)(RpVp) + (GIs/C2Rs3)((3Rp/Rs2)(ωp Rp) -ωp ))))Rs2/2))) / (ħ2/2(Erest/C2))))1/2(((1-(((2(Erest/C2)G / Rs) - (Isωs((((8πGTab/C4) + Λgab - Rab) * gab-1))1/2 + (S/(((3G(Erest/C2))/2C2Rs3)(RpVp) + (GIs/C2Rs3)((3Rp/Rs2)(ωp Rp) -ωp )))))/2(Erest/C2))+ (((8πG/3)((g/(2π)3)∫(((Erelativistic2 - Erest2 / C2) + ((Ar(X) + (ENucleon binding SNF ε0 μ0 /mu) - Ar(XZ±)/Z) / mu)2)(1/2)(1/e((ERelativistic - μchemical)/TMatter)±1)(ħωs + ħωs) - ((ksC2)/ Rs2) + (((8πGTab/C4) + Λgab - Rab) * gab-1))1/2(ΔKiloparsec)))2/(C2)))1/2) ∇' - (Cdt)2 = ds2 which dt in this case is tp Lastly, this was a typo (Universe Volumetric Planck State @ size of universe in radius) =(3/4)π ((1/(tpC2)) Luniverse RUniverse)3 It was supposed to be (Universe Volumetric Planck State @ size of universe in radius) =(3/4)π ((RUniverse/(tpC)) Luniverse )3 Luniverse = (∇Charge,∇Color,∇flavour,∇gravity - ∇Dark Energy) charge possible states per point (1,2/3, 1/3, 0,-1/3,-2/3,-1) Color Possible states per point(R,B,G,0,G,B,R) Flavour possible states per point (I,II,III,0,III,II,I) Gravity/Dark Energy possible states per point of space (Energy,Mass,Spin,0,Energy,mass,spin) as tpC = lp Every detail.

They both have gravity as Momentum and Rest Mass both create energy-stress despite which of these it is light has only momentum while it may not have Rest Mass still causes curvature as energy-stress under GR.

It is exactly as you think. A little deeper into this rabbit hole of "higher dimensions"

Yes, which is because despite being neutral in the view of Nucleons the quarks have charges which is actually a change in charge to some extent because the three charges are not literally on top of each-other in neutrons, there is a distance between them. Neutron absorbing can be a cause of Gamma emission and Beta Decay, this does very much screw with the nuclei doing that making it unstable.

That is true, but I didn't want to go into that detail, which branches from QM into QFT, He was referring to a static one of course that is true when you take in account SR of a Nuclei.

Ya, CharonY is correct, I was about to say the same-thing about this most bacteria do exchange genes via Plasmid Exchange, which is what our Germ-line sexual reproduction evolved from, this is not surprising despite bacteria still being asexual in reproduction.

refresh you posted before my last edit.

Here is a correct spinor of a S orbital