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VonBonfire
Well-known member
Yeah the coastline might flood and we'll all die without gene therapy. You're very much an alarmist.
Florida State Surgeon General Calls for Halt in the Use of COVID-19 mRNA Vaccines
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VonBonfire
Well-known member
OMG GET BOOSTED YOU SELFISH PRICK YOU"RE PUTTING US ALL AT RISK!!!!!!
Dan Gleesak
Well-known member
The coastline will most likely flood, but it has little to do with gene therapy.
Read up on tardigrades. Interesting stuff that I think will be commonplace on our lifetime, or at least mine
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VonBonfire
Well-known member
You put a lot of faith in science and technology which is fine but I think it is all shit.
Dan Gleesak
Well-known member
No you don’t
Laputan Machine
Well-known member
I am an expert at this. I know all about this. You are a science denier. You posted before getting vaxmaxxed. I'm telling your cuck club on you. Now you will be socially ostracized as punishment.
Ben Waylin
Banned
Well-known member
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VonBonfire
Well-known member
You can be obstinate but I pretty much hate all tech past 1965.
Dan Gleesak
Well-known member
I’ve never posted that. I’ve never given anyone shit for not being vaxxed either.
Dan Gleesak
Well-known member
People got to the moon with less tech than you use to post ignorant shit on the internet.
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harddriver
Well-known member
https://www.fda.gov/media/73667/download?utm_medium=email&utm_source=govdelivery
G. Biodistribution, Persistence, and Integration Analysis
Plasmid biodistribution, persistence and integration studies were initially recommended
to examine whether subjects in DNA vaccine trials were at heightened risk from the long-
term expression of the encoded antigen, either at the site of injection or an ectopic site,
and/or plasmid integration. Theoretical concerns regarding DNA integration include the
risk of tumorigenisis if insertion reduces the activity of a tumor suppressor or increases
the activity of an oncogene. In addition, DNA integration may result in chromosomal
instability through the induction of chromosomal breaks or rearrangements.
A typical biodistribution/persistence study assesses the presence of plasmid collected
from a panel of tissues at multiple time points ranging from a few days to several months
post administration. The panel of tissues typically includes the blood, heart, brain, liver,
kidney, bone marrow, ovaries/testes, lung, draining lymph nodes, spleen, muscle at the
site of administration and subcutis at the injection site. Plasmid levels are typically
evaluated using a quantitative real time polymerase chain reaction assay (Q-PCR)
validated for sensitivity, specificity and the absence of inhibitors. We recommend that
the sensitivity of this assay be sufficient to quantify <100 copies of plasmid per
microgram of host DNA. A claim of “non-persistence” requires that the amount of
plasmid at each site falls below this limit of quantification.
G. Biodistribution, Persistence, and Integration Analysis
Plasmid biodistribution, persistence and integration studies were initially recommended
to examine whether subjects in DNA vaccine trials were at heightened risk from the long-
term expression of the encoded antigen, either at the site of injection or an ectopic site,
and/or plasmid integration. Theoretical concerns regarding DNA integration include the
risk of tumorigenisis if insertion reduces the activity of a tumor suppressor or increases
the activity of an oncogene. In addition, DNA integration may result in chromosomal
instability through the induction of chromosomal breaks or rearrangements.
A typical biodistribution/persistence study assesses the presence of plasmid collected
from a panel of tissues at multiple time points ranging from a few days to several months
post administration. The panel of tissues typically includes the blood, heart, brain, liver,
kidney, bone marrow, ovaries/testes, lung, draining lymph nodes, spleen, muscle at the
site of administration and subcutis at the injection site. Plasmid levels are typically
evaluated using a quantitative real time polymerase chain reaction assay (Q-PCR)
validated for sensitivity, specificity and the absence of inhibitors. We recommend that
the sensitivity of this assay be sufficient to quantify <100 copies of plasmid per
microgram of host DNA. A claim of “non-persistence” requires that the amount of
plasmid at each site falls below this limit of quantification.
Laputan Machine
Well-known member
I don't care. Go get your booster. This should be #17 for you if you are not a science denier.
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VonBonfire
Well-known member
No one went to the moon but you and several others I know would qualify as space cadets.
Dan Gleesak
Well-known member
I probably won’t
Dan Gleesak
Well-known member
My point exactly
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VonBonfire
Well-known member
You didn't make any points. When do you think you'll melt down again?
Dan Gleesak
Well-known member
I think if I did get it, it would be #2
Laputan Machine
Well-known member
Then it is like you didn't get vaxxed at all. You are literally killing people by not getting boosted up to date.
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VonBonfire
Well-known member
It's not the in thing anymore. Other TGP'ers won't be impressed.
Dan Gleesak
Well-known member
Lol you’re a sad sad man
