[continued from previous message]

one of the things about the perfumed antibody pee test for cancer is that a math structure where if the detection rate finds one cancer in 10,000 concerned persons, and one false positive in 5,000 concerned persons, the likelihood that he cancer test
actually found cancer is only 1 in three; so the math of the part where treatment with a senolytic longevity and healthspan enhancing drug that also happens to be an anti-cancer chemotherapeutic drug causes decades of greater longevity and healthspan at
a well person and saves decades of living at each person when the drug effectively treats or cures the cancer; that makes treating a false positive, without using any followup tests or even medical practicioner visits, net beneficial to each individual,
and more net beneficial to the group as a whole. The nonoptimal part of course is that the person spends 10 weeks on rapamycin or dasimutib or someother chemotherapy drug, and likely feeling nonptimal while they are on it. So, at the developing world,
they could use senolytic anticancer drugs and skip actual visits to medical practicioners, further tests, imaging, and hospital stays; notably though, the cancer tests could only test for those cancers with a 90% pills-only cure rate. So if cancer were
detected with a 2.5 cent pee test, 9 out of 10 could be cured with just pills, and if the confirmationless test was a false positive the longevizing and healthspan of the senolytic anticancer drugs would cause net benefit to the treated person.

At the developing world, aligning promoted, automatic tests around things that have ultraffordable treatments could be a group longevity and wellness optimizing strategy; if social and fiscal resources could only cover a part of testing and treatment at
all the possible illnesses that might occur at the developing world.

dasimutib, molecularly modified to treat and cure the most curable cancers, that the perfumed antibody cancer tests looks for; dasimutib, or the actual name of the d-something-ib senolytic drug that is also a chemotherapy drug. It makes mice live longer
from the senolytic effect. Modifying name-like-dasimutib (tested with quercetain)(called DQ here) anticancer senolytic to be effective at treating breast cancer causes a numeric effect where DQ causes such a number of increased person-years of living

tamoxifen molecularly modified to be a longevity and healthspan increasing senolytic; notably wikipedia says tamoxifen is produced now with either yeast or bacteria at bioreactors, so a beverage yeast or yogurt bacteria source is a technology beneficial
at the developing world, decentralized and ultraffordable technology, that is apparently a slight modification of what already exists.

aminocurcurmin, curcurmin is like a 50% active senolytic at a graph I saw, so a modification to the curcurmin molecule could produce an anticancer chemotherapeutic drug. An ultraffordbale version produced at a plant or yeast might be possible as
curcurmin is already a plant product; as a plant product it is possible that even a modified curcurmin, like an aminocurcurmin, where the amino group placed on the curcurmin, or some peptide or protein on the curcurmin causes it to be actively
transported across the cytomembrane causing oncocytes to gather it.

perfumed antibodies increase sensitivity, resolution, and the number of chemicals that an immunochemical pee test can respond to

gel capsules are perhaps less than 1 cent, noting fiber optic magnifying a color, It seems possible that a particular shape of gel could magnify a 1mm sized immunodot, noting there are 21 of them at a three line imunnochemical pregnancy test to make them
5c and 1c gel magnifier

a new to me immunochemical diagnostic, like a dollar storepregnancy test, would be breathing out at a microstraw or regular sized straw so that moisture condenses, then having the immunochemical color shift chemical react to the exhaled condensate. I
have no idea what biochemicals concentrate at breath condensate, but they could make a list of all of them, and any that predicted or indicated wellness or illness could be the basis of useful antibody-color shift diagnostics. I perceive beverage
stirring microstraws might be less than 1 c each. the part where immunochemicals are printed, or rinsed through, the interior of the microstraw is one thing; It is possible that coating the microstraw (or full sized straw) with a deliquescent material
that liquefies when breath is breathed on it could make the immunochemical much more rapid to react, and able to react with less human moments spent blowing on the straw. Another possibility is that or, possibly NaPCA combined with a acylamide gel, to
make a fast inflating liquid gel reservoir with color change indicator at it, possibly making positioning of a “readout line” from a particular viewing angle, possibly near a part of the microstraw that had a lensish blob of plastic near the gel blob;
that way the more regular environment and structure of the NaPCA with polyacrilimide gel blob causes more predictable reactivity, and lens-located readability than colored NaPCA syrup would; also the gel blob technology could be near 1c as the amount of
immunochemical could be much less than the amount required to make an NaPCA syrup turn color enough to see. (although the microstraw might be another 1c) Also, with a condensate immunoscreening straw, the autohydrating gel blobs could be at a linear or
geometric array, and each blob at the arrary could report on the immunodetection of a different chemical. Although it could be possible to heap up or multiplex some immunodetected chemicals to provide benefit, for example, 10 immunochemical responses
that test fro cancer could all heap into one gel blob at a line or geometry of 7 or 20. If that one gel blob is nontransparent then perhaps there is a 1/3 or 2/3 chance the sample provider, who breathed into the straw

comparing immunoscreening the entire volume of a few liters of comparatively concentrated circulatory fluid with the few hundred ml of pee at a pee test, the number of different chemical-form or cytosurface things that can be antibody-glommed is
possibly tens of thousands of times to millions of times higher as to the number of available chemicals and outer cytostructure to a immonodiagnosis from, that means the diagnostic is much better at finding disease, or even finding wellness. Also, as
the perfumed antibodies release the perfume, which is another way of saying the chemically unique, high affinity, possibly linked to a molecule that the kidney preferentially excretes, reporter chemical (possibly a uniquely sequentially coded peptide or
biopolymer, the production of the peptide or biopolymer sequences could be automated so that they are automatically produced in peptide codes for digits 0 to 1 or 2,000) that is excreted at pee; Then when the person puts the

fizzy tic-tac or microcoated aspirin at 2 c to less than 1 c each. They turn blue to communicate that cancer chemicals were detected,notably at cancers that are very easy and affordable to cure.

Minimizing false positives at a cancer test: multiple simultaneous immunoactive diagnostic antibodies: find (immunodetect) say three chemicals, each a separate independent indicator of cancer, although the false positive might be 1 per 1000, three
chemicals have a combined preence false positive of 1 per billion. such as perfume from perfumed antibodies, but it could just be nonperfumed naturally occuring cancer predictive chemicals at pee. Also, although it seems possible to come up with a
different system, an immunochemical pee test, similar to a dollar store pregnancy test, could have histograms made from antibody-color bar segments. If the cancer bar was three rectangles high then it is the one false positive in a billion, three
antibody simultaneous response. If the cancer histogram bar is only one rectangle high it might just mean “think” or perhaps, “senolytics make you live longer and be weller, the cancer being tested for has a 95% cure rate from oral chemotherapy
alone, so you are in great shape if you just get the chemotherapy pills and take them” Then because the test makers and distributors have structured the antibody tests to find cancers that have high treatability, the person can have a medically
beneficial, senolytic, lifespan heightening cancer treatment that cures 95% of cancers of their tested type without further medical assistance, imaging, hospitalization or even physician contact. That makes cancer treatment, of cancers that can be
successfully be treated, much more affordable and also more widely treated at the developing world.

Depending on how you look at the numbers, an oral perfumed antibody pill could be as little as 5 C Online, one gram of various antibodies at bulk is $573, and imaginably, 100 nanograms could be a perfume antibody dose for glomming of just one chemical.
So that makes a 100 chemical diagnostic amplifying pill with 10 micrograms of antibodies, so at 100K doses per $573, the amount of C on the antibodies at each perfumed antibody pill is about one half cent per pill. Now the way the perfumed antibodies
are linked to ATP and have a numeric-like biopolymer antigen for the pee test to respond to goes with a 10 or 20 times higher C amount, so 5 to 10 c a pre-pee test pill that causes 1000 different body chemicals to be visible at a 5 C gel bead 1mm active
chemical pee test.

chronological interval of perfumed antibody delivery, ok, if you snort perfumed antibodies, they start circulating in 5-20 minutes, then possibly use another 20 minutes to glom onto some easy things at the circulation; If the perfumed antibodies perfume
part is attached to a molecule that the kidney preferentially excretes, then it is possible that diagnostic, detectable amounts of perfume accumulate at the bladder in 15-30 minutes. So 45-50 minutes after you snort it, a pee test diagnostic reads what
it says.

Comparing this to an oral perfumed antibody pill, an enteric coated pill, that fizzes automatically to dissolve at the part of the upper GI tract least destructive to antibodies; so it takes 4-6 hours before it fizzes and the perfumed antibodies can
commence a 4 hour absorption to the circulatory system period. At 4.5 hours the bladder concentration of perfume from the perfumed antibodies is high enough to diagnose with a pee test. So an oral version is 8-10 hours after dosing to getting a
diagnostic from the pee test.

Accumulation of perfume molecules at the bladder from attaching the perfume molecule to drugs that cause excretion of the chemical; (the perfume is after separating from the antibody that glommed a particular, protein, peptide, cytostructure, or chemical
at the body, notably all the capillary containing tissues as well as all the material at the circulatory system.

So, a perfumed antibody could possibly travel through a capillary, sometimes make its way to the cytes adjacent to the capillaries epithilial lining, and sometimes actually attach to the chemically unique antibody glommable outer surface chemistry of an
actual cancer cyte. Other times perfumed antibodies could just glom onto circulating biochemicals that are only produced at oncocytes, or possibly glom onto some protein or even leukocyte surface that goes with finding and glomming a systemic response
to oncocytes and oncostructures. These all utilize antibodies to find cancer, or find cancer is basent.

perfumed antibodies that leukocytes and macrophages eat: noting that the perfumed antibodies that get eaten, then possibly digested at the vacuole of a leukocyte or macrophage: The perfumed antibody could be constructed and engineered to have molecular
parts so durable they made it past vacuole digestion; the durable molecular parts being pooedout at the leukocytes or macrophages that leave durable molecular pieces that another different antibody is tuned to to cause a different perfumed antibody to
glom it, and send sufficient perfume to the pee to say “leukocytes at the body are eating things that TGW300 glommed onto. TGW300 attaches to: highly easy to cure cancer cyte surface protein. So if the other perfumed antibody that glommed the
biopolymer remains of the first immunochemical at the poo of the leukocyte or macrophage, is excreted at the bladder, then peeing on the test diganostic would say that leukocytes are meeting oncocytes at a person’s body.

Possibly strong popypeptides, or some other oligomer-like biopolymer like a custom-shaped starch (cyclodextrin or godel escher bach dextrin lumps that have high and unique antibody affinity), or the material degradable sutures are made from, or keratin.

perfumed antibodies at pee test during pregnancy describe fetal biochemistry from fetal metablic products that pass the placenta; paternity test while abortion pill still has weeks of available function and can abort if the pregnant person finds the
genetics, personality, or situation of the paternal gene source to be nonoptimal from the pregnant person’s perspective.


technology I do not know: a drug, that is actively beneficial to a fetus and possibly also the mother, possibly a snortable peptide or protein, that, like antabuse prevents drinking EtOH. People could take this to benefit their fetus and potential baby,
and as a side effect it would keep them from consuming EtOH, but I do not actually know how it works. some thing like antibodies to the actual eentsy molecule EtOH, that when they glom

perfumed antibody with fluorophores, three simultaneous antibody different chemical gloms, makes a 1 per thousand antibody glom false positive occurence go to a one per 100 million or 1 billion false positive occurrence if all three antibodies to
completely different chemicals are there simultaneously.

That multi-antibody response to build a diagnosis is beneficial as a fluorophore antibody diagnostic could test 1000 different chemicals at fluid from the circulatory system; fluorophore:ATP:antibody a fluorophore with an ATP linking it to the chemical
glomming antibody; when the antibody gloms, the ATP snaps off a PO4, and the fluorophore is then at the circulatory system, with part of an ATP such as an ADP or AMP attached to it, which makes it particularly distinguishable to the computer reading the
fluid sample at the test (noting there would be fluorophores attached to unglommed antibodies, and that telling the difference between these and reacted fluorophores antibodies produces daignostic data at the test)
engineering, chemistry, computer ic, computer fab, longevity, longevity technology, treon, treon verdery, physics, lasers, laser, emiconductor, dimension, math, IT, IL, pattern resonance, time travel, chronotechnology, circile, eric the circle, cartoon,
healthspan, youthspan, cpi, manufacturing, fiscal, money, software, petroleum, archive at deviantart com user treonsebastia

All technologies, ideas, and inventions of Treon Sebastian Verdery are public domain at JUly 8,2023AD and previously, as well as after that date

--- SoupGate-Win32 v1.05
* Origin: fsxNet Usenet Gateway (21:1/5)