15 Comments

Now *THIS* is REAL science. Dr. McKernan presents us with a thorough description of Dr. Sin Lee's methods and materials, makes the raw data publicly available, with minimal discussion. Great work that deserves to be saved, shared, and analyzed. Thank you, Dr.s, for your hard work and genuine contributions to Humanity.

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Jul 11, 2023Liked by Anandamide

Thank you Kevin McKernan for your work that has provided the wold with great advancements in understanding the molecular biology of the construct, and for keeping us updated on the related contributions of others.

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Jul 11, 2023Liked by Anandamide

Thank you Kevin. They rushed technology to market that was not ready. Is the mRNA platform complete trash? They appear to be switching to it for a lot of products - in my opinion, the main driver is profit, not human health. Peace.

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It's not meant to be ready. This has nothing to do with health. There is a greater agenda at play.

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100%. I agree. Thanks. Peace.

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It seems that the use of antibiotic-resistant sequences in the created plasmids may lead the whole of medical treatment for almost anything in this direction. Like prions, this feature apparently is transmitted/(contaminates) anything else it touches. Gene therapies may be the obligate result. {The unbidden question: or was it by design?} https://asm.org/Articles/2023/January/Plasmids-and-the-Spread-of-Antibiotic-Resistance-G

Wild times ahead.

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Thank you for the link. Peace.

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Fascinating! Thank you~

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Contamination or just simply what they put in there?

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The question is if the spike was ever produced by the modRNA or if it was always the DNA contamination.

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I suggest you read the substack which includes the sequencing of the Moderna vaccine.

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So in short answer, not all dsDNA fragments in the shot are long enough that comes with the SV40 promoter?

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author

This data shows there are fragments over 360 bases so the entire intact promoter is likely present in the shots.

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But not every single piece of fragment is 360 BP long right?

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author

We don’t have quantitation by size range.

A group in Japan noticed a 5X reduction in qPCR moving from 100bp to 300bp amplification.

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