Jikkyleaks 🐭 Profile picture
Jan 5 19 tweets 9 min read
#humpgate #TGAgate

1⃣ We found the humps.
2⃣ the EMA knew about them
3⃣ the analysis appears to be synthetic

@chrismartenson @stkirsch @Daoyu15 @Kevin_McKernan
Just a reminder that these are the same humps that we found in the TGA batch analyses here

They are contaminants at 3000nt and 2000nt length. The main mRNA should be about 4000nt length.
The EMA knew about these humps because they had them analysed. But only to a point.

Not only did they ONLY perform on analysis on the assumption of what they THOUGHT was in the product, but they accepted what now appear to be synthetic Western blots as evidence.
Here is the full document

The analysis was done by the Swedish Medical Products agency.
So someone spotted the humps that I also found and decided to separate them out from the main spike.

"Peak 1" is the non-spike RNA
"Peak 2" is the spike RNA
According to their analysis, the additional RNA had the 5'cap (which is the start of the RNA) but missed the end (the poly-A tail)

So it looked like it was broken fragments of the main RNA - but only the first part.

Where was the second part?
The whole fragment is 4284nt long. So if there is a 3000nt fragment with a 5'cap (with no poly A tail) there should be a 1284nt fragment floating around with a polyA tail!

Think of it like a lizard losing it's tail...
So what did they do to investigate this? Well, they assumed it must be spike RNA and therefore ran some Western blots (looking for protein) looking for spike protein fragments.

They showed that you need both the 5'cap and the polyA to produce the protein...
These are supposed to be Western blots with antibody staining each section of the spike protein (S1 and S2).

These showed that you need both ends to make spike.

You don't always need a polyA tail to make protein but OK, let's accept this.
Now they do the Western for Peak 1 (non-spike) and Peak 2 (spike) and stain with spike antibody.

The non-spike (peak 1) doesn't stain in either sample.

This means either it is not producing spike protein fragments, OR IT IS PRODUCING ANOTHER PROTEIN. Western blot as described in the document. Each black line i
In fact the document specifically requested "to further characterise the truncated and modified mRNA species present"

It's not just me.

Of course, that never happened. The only way to characterise these RNA fragments is by sequencing, and it has not been done.
So, to recap at this point we have:
1⃣aberrant mRNA at 3000nt and 2000nt, which cannot be a broken spike (4000nt)
2⃣those mRNA do NOT code for spike
3⃣no sequencing has been done to characterise the mRNA.
4⃣the fragments have 5' caps and are therefore active
Now the worst bit (as if the rest wasn't bad enough)...

Those Westerns are not right.

Here's what normal Westerns look like (this is from the same document). They are gels so they contract randomly, which is why nothing is ever a straight line.
(I'm not even going to start on the many different spike fragments in that gel).

Here are some more examples.

Note the typical features:
▶️Not straight lines
▶️Rounded edges
▶️Uneven lines/bars
Now let's look at the first gel picture in the document "from the sponsor"

It's the straightest gel ever.

Not just that....
But look how regular and symmetrical these bands are.

It's impossible.
It even contradicts their own gel in figure 8.

And the document itself is dithered which means...
The EMA have the original hi-res document with pictures and they copied it with dithering to black-and-white to obfuscate any attempts at assessing the probity of the gels.

Just to push the point, this is what happens when you synthesise an image like this with dithering.
So the Westerns appear to be totally fabricated. I'm happy to be proven wrong on this.

My guess is that the EMA or the Swedish medicines agency know that there is something else in that product, and it isn't degraded spike.

Oh well. Russian roulette it is.
h/t to @JM125reasons for providing this important document

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More from @Jikkyleaks

Jan 7
New FOI release from @USRightToKnow confirms that the Latinne paper - the subject of Peter Daszak's secrecy in respect of missing Genbank sequences - was submitted in August 2019. It discussed the origin of SARS-Cov-2, first touted in Dec 2019

nature.com/articles/s4146… ImageImageImage

Scroll down to Latinne et al... Image
Posted in April, just after the Daszak claim (linked in thread)....

Read 10 tweets
Jan 6
436 BILLION copies of spike protein circulating freely in plasma, a month after the Gene therapy vaccine.
In kids.
Their hearts will never fully recover.
You knew that, didn't you?

But there is more than that here...
THREAD [repost]

ahajournals.org/doi/suppl/10.1… Image
Note: This is a repost of an earlier thread that contained an important typo that I felt required a full thread rather than a correction at the end.

To avoid any claims of "misinformation" given how important this is, and how much the thread took off.

Let's resume
This is the damning graphic.
The vertical scale is a log scale.

The line at about 15pg/ml is the limit of detection, which is why the blue dots are there. There are still up to 100 billion molecules of spike in those patients - 20 days later. Image
Read 14 tweets
Jan 6
BREAKING: After uncovering gross incompetence (or negligence) at the TGA @SenatorRennick asked them what they did about the clearly contaminated batches.

Their response:
"We didn't see any problems"
#humpgate #TGAgate ImageImage
The response confirms that the TGA were not competent to assess this product, given that the EMA identified the contamination.

Full thread below:

This response was completely disingenuous because you cannot find a protein that you are not looking for.

Without mRNA sequencing (which they didn't do) they would have no idea what protein to look for.

Protein sequencing is complex, but they didn't do that either. Image
Read 5 tweets
Jan 5
Li-Meng Yan is so incensed that I dared to question the #CCP narrative that she not only retweeted her own tweet (which misrepresented mine) but I received a whole host of CCP bot followers and trolls.

Thanks @DrLiMengYAN1
Just to clarify, the tweet was a rebuttal of some account that claimed I had "lost credibility".

There was no disparaging of any tragedy.

It was purely about the staging of the picture....
No problem, just unfollow me.
So why did Li-Meng take such an interest?
So whose side is she on?
I have never been sure since in her first account she seemed to promote the mRNA vaccines.
In this account she is mixed.
Read 13 tweets
Jan 3
According to TGA DAEN a 17 year old boy died following administration of the Pfizer vaccine

The death was reported on the 2nd Sept 2021, which means it occurred prior.

One (in)famous death of a 17 year old occurred at that time.
@SharonC59122606 @_real_babaG @JesslovesMJK
I guarantee you won't be able to read this and watch the video clip without shedding a tear
At that time the principal of the school declared that Tom - a top grade swimmer - died after getting chest pain on getting out of the pool.

It wasn't a "sudden death" as seen - rarely - in young people during sport. It was described as a heart attack. In a healthy 17 year old.
Read 14 tweets
Jan 3
Can you see how it works?

The same "Australian guideline" which was coordinated by the MAGIC consortium (not Australian at all) that prohibited antibiotics in the treatment of #COVID pneumonia....

Told you what the standard treatment was in China
@chrismartenson #3Tablets
Ignore the Interferon in this RCT.
It doesn't matter.
What mattered was that China was using HCQ and antibiotics.
Their death rate per capita was the lowest in the world.
Impossible for a "novel" virus.
This is the paper. No deaths.
HCQ + Vitamin C + Azithromycin as "standard care"

This was standard care in Australia up to March 2020.
Then blocked by the
Then the deaths started.

Read 8 tweets

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