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Ha,ha, Elizabeth Holmes operated one of the biggest scams in American history.
antibody is "a blood protein produced in response to and counteracting a specific antigen. Antibodies combine chemically with substances which the body recognizes as alien, such as bacteria, viruses, and foreign substances in the blood"
Agreed. I was thinking about it and came to the same conclusions you did.
It's all in the timing.
We need Mark to explain what the Arrayit test can detect earlier than other antibody tests. Maybe he found some protein that is activated earlier than the other antibodies. Who knows?
IMO Arrayit must be feeding this info to their distributors. I doubt they make it up.
No, somebody posted about it about a month ago. I bookmarked it and reviewed again today. That sentence jumped out at me.
After suspension and downgrade to the greys, it was destined to trade in the double or triple zeroes.
So a higher 0.01, 0.012 may have to do with the test being on the FDA list and being sold.
Hmmm. Something to think about the Arrayit test. But I need to be convinced.
Last week there were 24 labs that had notified the FDA that they had validated a test for covid-19 and they were selling it.
Today the list is 14 labs. Arrayit is still on the list.
Arrayit Corporation
BioDiagnostic Inc.
Center for Cellular Therapy Medical University of South Carolina
DLS Research & Ventures
EDP Biotech Corporation
Emory Medical Laboratories
Enzo Clinical Labs
Genalyte, Inc
IMMYLabs
KSL Diagnostics
University of Arizona Genetics Core for Clinical Services
University of Minnesota Advanced Research and Diagnostic Laboratory
Vibrant America Clinical Labs N
White Coat Sciences
Showing 14 entries
Thanks for the update.
It made more sense to get to the covid-19 page when you clicked on the covid-19 box .
It's backwards to get the information about the test after you press the button "order your allergy and COVID tests today".
And what if you want to order the covid test only.
Before they had a page to order the allergy test and a page to order the covid test.
I'm sure the arrayit.com web pages are nowhere near completion, but they put in production.
Also, they need to put it through spell check it's
"personnel not "personelle"
Somebody created that Fake Arrayit Corporation @ArrayitCorp account
Joined May 2020
https://mobile.twitter.com/ArrayitCorp
Real Arrayit Corporation @arrayit account is
Joined March 2009
https://twitter.com/arrayit?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor
Agreed.
You really think things work that fast in a federal bureaucracy, or any bureaucracy for that matter.
A notification is received by an official, and BAM that same night the IT department makes the change.
I have no doubt the FDA updates the list frequently, but it does not answer what's the time period between the FDA receiving a notification and their updating the website with that notification. For all we know it could be days.
It's all a confusing play on words as to what FDA action meant to many people.
FDA allowed Arrayit to sell the test. But it's not "reviewed/ approved" or "Emergency use authorized".
Many people, icluding in the media, don't understand the distinction of the 3 terms.
OK I take your word for that. But how about: How long does it take for the FDA to post a company on the website after they have notified the FDA?
That's the day we happened to see it there, but it doesn't prove that's the day it was posted on the FDA website.
Also how long does it take for the FDA to post a company on the website after they have notified the FDA?
You are inserting your opinion FRAUD in the official SEC statement.
Can you tell us which day it appeared on the FDA list of labs? And also how long does it take the FDA to update the list online after a company notifies the the FDA that they have a test?
Good find. Arrayit SARS-CoV-2 (COVID-19) Screening Test
I tried it again tonight, and you can't jump to the new webpage anymore by clicking on the covid-19 picture from the main page. When you do that you get the pdf file of instructions.
It could be that the new page is a work in progress. I did see that they changed IgE to IgG as you said in another post. Obviously they did not proof read it before.
The Roche test is an antibody test, but not a rapid test. It takes a couple of hours to process. And it uses blood from a vein
The Roche test is 100% specificity and 99.8 sensitivity
The question is who the SEC thinks was running the pumping. If Arrayit was not part of it, then that should be the end of that part of the investigation
Interesting article. If Mark is using both IgG and IgG that would really make the test different from others especially if it's more accurate and gives more information about the infection.
I know the can test both. But IgG is what's typically used in covid-19 antibody tests. IgE is for allergies.
On the website http://www.arrayit.com/SARSCoV2.html they mention both about covid, it's confusing. Is it a typo when they wrote IgE?:
I thought they were measuring IgG. Are they also using IgE? or is that a typo?
IgE is what they use for the allergy test.
Clever. Great catch. Those links weren't working before.
Thanks for the website updates!!
How did you find the webpage with all the new wording about the covid test http://arrayit.com/SARSCoV2.html
The plain arrayit.com doesn't have the updates
Good catch Delsurfer. I hope people are not feeding the SEC info that's backwards.
If you're talking about 10 days to send validation data to the FDA about the covid test and submit an EUA request, that applies only to commercial manufacturers of tests, not to CLIA labs like Arrayit.
CLIA Labs have the option to apply for EUA. The FDA encourages them to do so, but it's not mandatory. Arrayit can sell its test without objection from the FDA.
Nevertheless, I believe (see below) that Arrayit has submitted an EUA and is waiting for the authorization. So in essence the FDA wait is in progress.
IMO If the SEC is investigating the company, it will communicate with the company, and the company through its lawyers cooperates in the investigation. Any information that could help satisfy the SEC's concerns will help.
They got suspended because of "information in the marketplace" claiming that the covid-19 test was FDA approved. After the suspension was over it started trading in the grey market.
If the company can prove to the SEC that a) they do have a test that the FDA does not object to the company selling and b) the company was not involved in the "FDA approved information" it would help their case.
a) is a already proven fact according to the FDA website.
Since Arrayit is a CLIA lab, validated its test and notified the FDA, the FDA does not object to them selling the test as long as some disclaimers about diagnosing covi-19 are included.
If they can get the EUA, that's another feather in their cap, but it's not required.
Another conspiracy theory?
Yes it can be proven.
otcmarkets has the transfer agent verified share structure.
With the exception of the 72M restricted shares issued to Iconic last year, the O/S has not changed in years.
Market Cap Market Cap
13,518,027
05/07/2020
Authorized Shares
2,480,000,000
04/27/2020
Outstanding Shares
1,126,502,244
04/27/2020
Restricted
82,713,440
04/27/2020
Unrestricted
1,043,788,804
04/27/202
https://www.otcmarkets.com/stock/ARYC/security
Scorpgirl, Do you have access to the article? I don't want to pay to subscribe just to read this story. I think it says the one company that escaped is Arrayit
I don't follow when you say IF.
They do have a test that they validated, notified the FDA and they are selling them because the FDA doesn't object.
So 6 have dropped out this week.