Amir Rahmani
@astormic.bsky.social
740 followers 400 following 180 posts
Super-resolution microscopy enthusiast Postdoc at the University of Cambridge Visiting Researcher at the British Antarctic Survey College Research Associate at Wolfson College https://laser.ceb.cam.ac.uk/
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astormic.bsky.social
But does it have to be H-1B visa?
Reposted by Amir Rahmani
kahsage.bsky.social
@tanner-fadero.bsky.social told me there was a discussion about the unofficial name for #snouty V3. We have had Mr. Snouty and King Snouty, and there were people suggesting Emperor Snouty. I think it is time for a Lady or EMPRESS snouty. I have created Art to support this.
astormic.bsky.social
Thrilled to see interest in this preprint! This work was a major part of my PhD, my hope is that single-molecule flow cytometry can be useful to the community in exploring new applications and discoveries.

doi.org/10.1101/2025...
astormic.bsky.social
I’ve never had that privilege!
astormic.bsky.social
I really need a keyboard blocker like this!
astormic.bsky.social
Huge thanks to an incredible team who made this possible 🙌 especially Aleks for his great supervision and support.
astormic.bsky.social
We applied smFC to triple-negative breast cancer (TNBC) cells:
📊 Found 30% of cells express low-abundance c-kit.
🧬 This subpopulation was invisible to standard flow cytometry, but smFC revealed it.
astormic.bsky.social
With smFC we achieve:
✅ Digital precision down to ~2–3 molecules/cell
✅ 10–80× improved detection limits vs. conventional FC
✅ Quantification of membrane proteins in high throughput, single-cell detail
astormic.bsky.social
smFC combines:
🔬 High-NA oblique plane microscopy (OPM)
💧 Microfluidics
✨ Superbright, large Stokes shift dyes
→ enabling optical sectioning + photon efficiency needed for single-molecule detection in flowing cells.
astormic.bsky.social
Conventional flow cytometry is powerful but has a blind spot:
❌ It can’t detect proteins expressed at very low levels (<100–1000 molecules/cell).
That means many weak but biologically crucial signals are invisible.
Reposted by Amir Rahmani
tanner-fadero.bsky.social
How many photons are in a GFP? — more than last year, and more than you thought. Here's a simple, cheap, and practical method to break a fundamental limit in fluorescence microscopy. But it only works in light sheet!
Reposted by Amir Rahmani
truenorth-ia.bsky.social
I was searching for a Python utility for Fourier Ring/Shell Correlation. All I got in a blue sky search were 4 small posts from @christletx.bsky.social ... all I got from chatgpt was installation instructions for non-existent libraries and github repos... anyone know a good tool for this?
astormic.bsky.social
That makes perfect sense!
astormic.bsky.social
Excellent work Johannes!

Would SST work for long docking strands (70–80 nt, like in DNA-PAINT SPT)? I believe ROS-induced damage is the primary cause of degradation in longer strands too, but they may be more vulnerable.

Also, does sodium sulfite affect buffer viscosity or refractive index?
astormic.bsky.social
I can't imagine there is any other way!
Reposted by Amir Rahmani
gebhardtlab.bsky.social
The review on live-cell SMT that I contribute to the jmolbiol.bsky.social special issue ‚Imaging of the central dogma‘ is now online as pre-proof: www.sciencedirect.com/science/arti...
Reposted by Amir Rahmani
jsdaniel02.bsky.social
Production has started for a new #Snoutscope objective, AMS-AGY v3. It has significantly larger FOV and some other tweaks from v1 and v2. Currently accepting pre-orders. The price will need to increase modestly after deliveries start late October.
comparison table for v2 and v3
Reposted by Amir Rahmani
genesdev.bsky.social
📽️ G&D Tapes 📽️

G&D author, Noah Helton tells us about their new study in #genesdev, revealing an intriguing link between stress granule formation and the integrated stress response. #OpenAccess @smslmoon.bsky.social

Read the full story here:
➡️ tinyurl.com/gd352899