KruegerLab
@kruegerlab.bsky.social
300 followers 340 following 26 posts
Molecular Immunology Lab, FB08 Biology and Chemistry, Justus Liebig University Giessen, Germany uni-giessen.de/fbz/fb08/Inst/…G
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kruegerlab.bsky.social
Congrats James! Well deserved!
kruegerlab.bsky.social
We‘ll give it a go 😀
Reposted by KruegerLab
labliston.bsky.social
For our #flowcytometry peeps, would you like to have a single fix/perm protocol that is optimised for everything? One that preserves fluorophores while allowing simultaneous TF and cytokine staining? How about 100-fold cheaper?

You got it:
currentprotocols.onlinelibrary.wiley.com/doi/10.1002/...
currentprotocols.onlinelibrary.wiley.com
Reposted by KruegerLab
eurjimmunol.bsky.social
Awesome performance of the band composed of great immunologists, including our Editor-in-Chief Matteo Iannacone behind the keyboard, at the #IUIS2025 Congress Party! 🎹🎸🎶
Reposted by KruegerLab
eurjimmunol.bsky.social
Steffen Jung announced Andreas Radbruch as keynote speaker at #IUIS2025, highlighting his strong support for European Immunology and the importance of backing EJI and European research!

Andreas presenting his newest EJI article by Schneider-Revueltas et al. onlinelibrary.wiley.com/doi/10.1002/...
Reposted by KruegerLab
rtg2355.bsky.social
Back from another great retreat to Schmitten, Taunus - this year with guests from @4r-rtg.bsky.social and from @jlugiessen.bsky.social and @mpi-hlr.bsky.social core facilities. We had inspiring method sessions on scientific diagrams & statistics, complexome proteomics, microscopy & image analysis ..
kruegerlab.bsky.social
Congrats! I really hope that this approach to science will set an example for many.
Reposted by KruegerLab
taghonlab.bsky.social
Our research on human γδ T cells is in collaboration with the lab of David Vermijlen @ulbruxelles.bsky.social
u-cri.ulb.be/index.php?ac...
In this context, he is looking for a postdoc with experience in molecular biology. Apply now to become part of the team! 👇
euraxess.ec.europa.eu/jobs/306959
kruegerlab.bsky.social
This was a joint effort of our lab spearheaded by Heike Kunze-Schumacher and @probertimmodels.bsky.social and great collaborators including @victorgreiff.bsky.social and Michael Meyer-Hermann. Thanks to @dfgpublic.bsky.social for their continuous support!
kruegerlab.bsky.social
Taken together, we provide a framework to quantitatively determine cell cycle phase duration in vivo, which can be applied to a broad variety of biological systems.
kruegerlab.bsky.social
We showed that thymocyte cell cycle phase progression is heterogeneous and that, in a model of irradiation induced involution followed by endogenous regeneration, cell cycle re-entry and G1 shortening promote thymus regeneration.
kruegerlab.bsky.social
We discovered that a stretch model of simultaneous expansion or contraction of G1 and S phases explains steady-state thymocyte cell cycle speed transitions.
kruegerlab.bsky.social
We combined sequential dual-nucleoside pulse labeling and DNA content analysis with two different agent-based mathematical models to map cell cycle phase durations in thymocytes in vivo.
kruegerlab.bsky.social
Well. Perfect Q. Bullet proof glass yes. Jewish elementary school in Germany.
kruegerlab.bsky.social
None of this would have been possible without the fun and productive collaboration with the Zarnack lab at Goethe University Frankfurt.
Thanks go out as well to our funders @dfgpublic.bsky.social (CRC902 and RTG2355).
kruegerlab.bsky.social
Main conclusion: Functional analysis of miRNA binding sites in physiologically relevant context massively expands the pool of miRNA-mRNA interactions.
kruegerlab.bsky.social
Prominent 3' binding in MREs exists and contributes to miRNA functionality in a complex manner.
kruegerlab.bsky.social
We also uncovered a group of target sites associated with repeat regions in KZFP Zn-finger transcription factors, which behave differently. Located predominantly in the CDS, they act through translational repression.
kruegerlab.bsky.social
There are many more binding sites than are predicted in silico.
While established targeting rules apply in general, we identified many functional non-canonical MREs.
We uncovered a prominent mismatch in the seed match, which retains functionality, thus extending the pool of targets substantially.

kruegerlab.bsky.social
Using combined oligo-enriched eCLIP, RNAseq and ribosome profiling, we wanted to identify functionally relevant targets of miR-181. What did we learn?