Great work again. Forensically unraveling this mess piece by piece and so great to see this being done by different scientists across the globe, all validating and enhancing each others work. The language barriers will slow this down but the truth will out eventually .....
Cells that received a DNA fragment with the SV40 promoter and the neomycin resistence gene (neoR/kanR) would produce the protein "neomycin-kanamycin phosphotransferase". This protein would be detectable by immunostaining or ELISA and possible antibodies produced by the patient would also be detectable.
The vaccination cannot be undone. Of course the immune system does its best to eliminate mutated body cells.
"The SV40 early promoter contains at least three spatially distinct elements: (1) two 72-bp repeats comprising the enhancer sequence; (2) three 21-bp repeats, each containing two (G + C)-rich motifs; and (3) the TATA box or Goldberg–Hogness box." https://www.sciencedirect.com/science/article/abs/pii/S0079660308603499?via%3Dihub
Keep going. I hear the groan of inevitability churning in the background!
What blood test would reveal presence & what counter for elimination ?
IF ELIMINATION POSSIBLE ..?
What are the implications of this? Cancers, I assume?
Yes. Lots. Metastatic.
Great work again. Forensically unraveling this mess piece by piece and so great to see this being done by different scientists across the globe, all validating and enhancing each others work. The language barriers will slow this down but the truth will out eventually .....
Reverse Engineering of Pfizer jabs is wonderful!
Do you have a Molecular Weight calculator for the 72 bp insert, or any other interesting sequence of the string?
I would expect some gel electrophoresis controls here at the very least. Couldn't these just be artifacts of the assembler and tools being used?
Have you read all the other substacks from February 16th, which detail the methods etc?
Cells that received a DNA fragment with the SV40 promoter and the neomycin resistence gene (neoR/kanR) would produce the protein "neomycin-kanamycin phosphotransferase". This protein would be detectable by immunostaining or ELISA and possible antibodies produced by the patient would also be detectable.
The vaccination cannot be undone. Of course the immune system does its best to eliminate mutated body cells.
Not if the vaccine hits immune privileged cells.
Multiple studies show spike and nucleic acids persistence suggesting the immune system isn’t clearing these things in some people.
"The SV40 early promoter contains at least three spatially distinct elements: (1) two 72-bp repeats comprising the enhancer sequence; (2) three 21-bp repeats, each containing two (G + C)-rich motifs; and (3) the TATA box or Goldberg–Hogness box." https://www.sciencedirect.com/science/article/abs/pii/S0079660308603499?via%3Dihub
The sv40 t antigen attaches to the oligomeric complex causing amyloidosis.
It’s illegal to steal live inventory.
The analysis can only be performed on expired lots.
If they had nothing to hide they would allow access to the lots for testing.
Covidissonance: when qPCR is quantitative for viral detection but non-quantitative for vaccine detection.