Anonymous ID: 2d0d85 Jan. 20, 2022, 3:58 p.m. No.15424787   🗄️.is 🔗kun   >>4894

are these on slides with a coverslip or is this in a dish?

ive seen (some) artifacts similar to this from the fixation protocol on a slide, but if its in a dish or a slide without a coverslip then yeah, looks like you at the very least are showing they are contaminated with something

Anonymous ID: 2d0d85 Jan. 20, 2022, 4:18 p.m. No.15424919   🗄️.is 🔗kun   >>4934

>>15424894

like these

>>15424551

>>15424509

or this one ive seen with an air bubble,

>>15424422

but like i said that was with fixation, looking at cellular tissue, i doubt you would have used a fixative for a liquid, but just wanted to point out it looks similar.

im assuming you're doing this in a lab? if you have any left, id put some into a 24-48 well plate, dilute it with distilled water and possibly DMEM if you have it, pop it in the incubator for a few days and take pics every day, just to see if the contaminant is organic or not

Anonymous ID: 2d0d85 Jan. 20, 2022, 6:03 p.m. No.15425553   🗄️.is 🔗kun   >>4886

it definitely has no microarchitecture, as in its not a normal cell body with distinct organelles

might be synthetic, at this point i doubt this is all artifact

how many slides did you make from the two vaccines?

Anonymous ID: 2d0d85 Jan. 20, 2022, 6:05 p.m. No.15425578   🗄️.is 🔗kun

if you have sample left and a glass bottom 24 well plate id definitely mix it with dmem, you might find something interesting, worth a shot

Anonymous ID: 2d0d85 Jan. 20, 2022, 6:11 p.m. No.15425618   🗄️.is 🔗kun

ideally you'd want to send a sample to genomics and mass spec but both of those are gonna cost a shit ton of money and leave a paper trail unless you have a friend running the core, or have a rig you can use