Clinical pathology
One section, one stain, one answer. Serial slides break spatial context and consume irreplaceable biopsy material.
Our technology can resolve more than thirty protein markers in one intact tissue section, giving your team spatial proteomics with the clarity of single-plex immunofluorescence.
Every laboratory working with limited tissue faces the same trade: more markers, or more sections. SPECTRE-Plex removes the trade entirely.
One section, one stain, one answer. Serial slides break spatial context and consume irreplaceable biopsy material.
Marker panels grow faster than sample volume, forcing teams to choose which biology they are willing to lose.
Immune context decides whether a mechanism reads as signal or noise — and it only appears when markers coexist.
We are building an imaging platform where spatial truth is preserved — where every marker keeps its coordinates, every cell keeps its neighbours, and one section carries the whole story.
Chemistry, optics and reconstruction tuned as one system, so multiplex depth arrives with less bleed-through, less photodamage, and more confidence in every channel.
PLATFORM
Swap marker panels, cycle counts and reagent modules without re-engineering the workflow — the same cyclic chemistry scales from a pilot panel to a full spatial proteome.
Automated stain and photo-inactivation cycles run unattended on a single mounted section, cutting technician time to a fraction of legacy multiplex protocols.
An optically invisible microfluidic window delivers high-NA, aberration-free optics, resolving subcellular detail that lower-plex fluorescence methods miss.
Morphology-aware analysis and open data formats carry results straight into any pipeline, from a single slide to translational cohorts run in parallel.
COHORT SCALE
Our Casper Chamber system allows multiple slides with tissue microarrays to be simultaneously stained and imaged with the same multiplex marker panels, allowing rapid and scalable data generation for translational cohorts with minimal batch-to-batch variation.
PATENTED ENGINE
Patented imaging chamber
A microfluidic “invisi-slip” chamber built around a refractive-index-matched optical window. Any high-NA water-immersion objective mounts without custom optics, so your lab scales marker count and sample throughput on hardware you already run, cycle after automated cycle.
Patented reagent series
Dye-inactivation and quench chemistry that clears fluorescent signal between rounds orders of magnitude faster than legacy bleach reagents — no gas bubbles, no morphology loss — so panels expand marker by marker without extra hands-on time.
Invented at Boston Children's Hospital and Harvard Medical School, the Casper chamber and ECTO reagent series were validated together in a peer-reviewed 22-marker, seven-round cyclic imaging panel resolving healthy and active celiac disease duodenal tissue at single-cell resolution.
PEER-REVIEWED
Independent findings in Communications Biology and the Journal of Pathology Informatics confirm our imaging and analysis platform delivers reliable, quantitative results on real diagnostic tissue.
Communications Biology · 2025
Peer review confirmed the Casper chamber and ECTO reagent chemistry resolve a 22-marker, seven-round panel in eight hours, validated in pediatric celiac disease duodenal tissue.
Journal of Pathology Informatics · 2025
La and colleagues validated an automated villus-crypt evaluator against our multiplex imaging output, confirming reliable, quantitative scoring of mucosal architecture directly from high-plex tissue scans.
Send us your experimental scenario and we will work with you on a multiplexed panel and a feasibility read on your own tissue.