From: treon3verdery@gmail.com   
      
   Rapamycin is a nootropic that can heighten laboratory mammal cognition and can   
   keep me awake, brain positron emission tomography could find out which neuron   
   types, and at what brain location these effects occur from, other nootropics   
   that activate these    
   areas could be screened for longevizing effects, also if rapamycin is   
   concentrating at some regions of the brain, or some neurotransmitter types and   
   not others then a molecular variant of rapamycin that goes to all brain areas   
   and all neurotransmitters    
   could be found    
      
      
      
   Longevity gene, neuron types where one neuron uses a particular    
   eurotransmitter or just all the cytes at the body could use epigenetic   
   modification drugs to make fewer mTOR receptors and possibly increase the   
   amount of AMPK receptors at neurons, causing    
   the CNS to be more youthful possibly causing longer duration of youthful mind,   
   and youthful cognition, and youthful emotion, cardiovascular system cytes   
   could also be beneficial, causing greater longevization, youthspan of the   
   heart and vasculature, this    
   could be a one dose drug that prevents cardiovascular disease   
      
      
      
   Create epigenetics that reduce activity of mTOR receptor producing genes, and   
   possibly heighten production of AMPK from AMPK genes, possibly through   
   screening a million or to find an even more optimal epigenetic modifier, tens   
   of millions of molecular    
   variants of epigenetic modifying molecules to one that is most specific to   
   downregulating mTOR, and up regulating AMPK, this could have multi generation   
   longevizing effects, germline or also oocytes and spem modification to have   
   the epigenetics of    
   longevity is beneficial   
      
      
      
   Modifying the genetics of cytes used at nuclear transfer to oocytes to have   
   mTOR epigenetics that cause greater longevity   
      
   Liposomal ultra micro reactors   
      
   Aluminum or other atom hydrophilic or electrically charged head, or at another   
   solvent like NH3 or DMSO, Or silicone oil, charged silicone distal   
   electronegativity oil, make liposomes or things like silicosomes with   
   reactants at the liposome or    
   silicosomes cores, sequential liposome or silicosome dipping might even   
   combine reactants that are non able to occupy the same flask, then a   
   detonation, warmth occurrence, photochemistry, like lasers event, or radiation   
   occurs and the comparatively few    
   atoms interior to the liposome react to form a product at the core of the   
   liposome, liposomes are kind of see through and liposomes can be sorted with a   
   spectrophotometer at a thing like a flow cytometer, or possibly liposomes or   
   silicosomes could have    
   surface charge that varies with core contents possibly from making the   
   silicosome with 1/100th highly C=C saturated with NH  on it or zubbles (TM a   
   kind of plaything) like chalcones, which are so responsive that without   
   disintegrating they change color    
   based on surface tension) then based on what is in the liposome the surface   
   chemistry differs facilitating sorting, a trillion liposomes with 1000   
   reaction production product molecules each makes about 2^14 atoms or a   
   billionth of a mole, at a 100 amu    
   product that is 1 microgram of product, flow cytometry to centrifuge   
      
      
      
   Silicosomes can be made with solventophilic heads and multimers with   
   electronegative (like nitrogen, phosphorus, metals, Se ) atom heads, it is   
   possible to omit carbon funkiness (what happens after an actual lipid liposome   
   is warmed or disintegrated with    
   light or radiation), the non interactivity of the reactant molecules with the   
   Si silicosomal interior perimeter makes things cleaner   
      
      
      
   The reacted silicosomes do a laser spectroscopy and flow cytometry like   
   traversal of a tube and are sorted into products, so a reaction that yielded   
   100 products then produces 100 different separated products, possibly a   
   million at a microfluidic device (   
   a million channel microfluidic chip I read about), and if these are products   
   like longevity chemicals they can then move to an organism area to find out if   
   they are longevizing, so 1 million varieties of halogenated rapamycin can be   
   silicosomal reaction    
   produced, spectroscopy sorted, then applied to yeast or human tissue culture   
   microfluidically, a trillion silicosomes could be 1 microgram of product, at a   
   300 mm wafer with 10-100 billion wells per chip, 1 million variants of   
   longevity molecules tested    
   per notable source, things like endolith chemicals  autovariationized  is 10k   
   sou   
      
      
      
   Longevity technology   
      
   Yeast have longevity chemical responses, find another organisms, possibly even   
   another yeast, that responds like yeast to a library of 10k different   
   chemicals but has a 4 hour lifespan, also verify that when tested at the 4   
   hour lifespan 40-100 different    
   longevizing remain longevizing, then use that organism  to screen new   
   longevity chemicals in just 4800 minutes to 240 minutes each, so at the   
   reacted sorted liposomes microfluidically connected to a 10 billion well yeast   
   IC plate then after just 1/3 of a    
   day you would be able to know longevity had more than doubled, and based on   
   well location, which chemicals were associated with the longevity heightening,   
   and then make a completely new liposomal reaction 10 billion chemical library   
   to screen on another    
   plate, that screens about 30 billion new longevity chemicals each 24 hours or   
   1 trillion new longevity chemicals a month    
      
      
      
   Are buckycup liposomes possible   
      
   That's like 1 nm or less buckycup like electron wave concentrating   
   semiconductor manufacturing chemical or nano technological reaction/assembly,   
   integrated circuit technology geometries technology   
      
      
      
   Noting 1 nanometer dots are likely possible with 3nm integrated circuit   
   feature technology with a more casual error rate,  then a 300 mm wafer has   
   about 9 times 10^12 one nanometer features,  a 1 nm diameter well 5000 nm deep   
   (5 micrometers) is a stack    
   5000 molecules deep and one molecule wide (carbon 120 picometers, about 9   
   carbons to a well width) that could be sequentially piled up in the well to a   
   depth and volume of 45,000 molecules, this makes me think of things like, load   
   it up, use radiation to    
   initiate reaction or polymerization,  or radiation to divide things like   
   halogen atoms from their molecules to do new reactions, or load some areas   
   with catalytic molecules like electrically addressable liquid crystal   
   molecules with cobalt or Rh atoms on    
   it to do chemistry, may also be cycled between a temperature with 1/2 the   
   reaction rate and one with the full reaction rate to load it when cool, light   
   and charge based reactions are also cool,   
      
      
      
      
   [continued in next message]   
      
   --- SoupGate-Win32 v1.05   
    * Origin: you cannot sedate... all the things you hate (1:229/2)