THE PLATFORM

From liquid biopsy to
structure-resolved 3D data.

Nebulum preserves fragile circulating objects from whole blood, immobilizes them in an optically matched matrix and converts the complete volume into population- and event-level research endpoints.

Nebulum workflow from blood collection through a three-dimensional matrix to volumetric analysis
ONE CONNECTED WORKFLOWBlood → matrix → image → quantify

From liquid biopsy to a
structure-preserving 3D matrix.

Stabilize fragile circulating structures, concentrate the retained specimen and embed it in an optically matched matrix for complete volumetric measurement.

One continuous specimen journey from liquid biopsy to spatial measurement.
01
PRESERVE

Stabilize labile structures at collection.

02
CONCENTRATE + EMBED

Retain rare objects in a thin 3D matrix.

03
IMAGE

Acquire the complete volume through depth.

04
ANALYZE + QUANTIFY

Segment objects and compute burden, morphology and spatial endpoints.

ONE SAMPLEPopulation context, without losing event-level spatial structureONE REGISTERED MATRIX

From whole matrix
to spatial phenotype.

Measure the complete capture volume, then reconstruct individual traps as registered three-dimensional objects for event-level biological analysis.

ONE MATRIX · POPULATION TO SPATIAL PHENOTYPE
Whole-gel matrix containing morphologically diverse extracellular DNA-trap eventsThree-dimensional extracellular DNA-trap reconstruction with associated neutrophils
01
Whole-matrix context

Measure the complete capture volume before selecting an individual event.

Whole-gel extracellular DNA-trap matrix01 / WHOLE MATRIX
SELECT ONE REGISTERED EVENT
Registered three-dimensional extracellular DNA-trap event02 / 3D SPATIAL PHENOTYPE
01Population burden
02Trap morphology
03Marker colocalization
04Cell–trap relationships

What the platform
turns into data.

The output is not a single fluorescence value. Each measurement retains its relationship to the complete matrix and the original three-dimensional event.

01

Population burden

Count, area fraction and distribution across the complete capture matrix.

02

Trap morphology

Size, branching, compactness, porosity, aggregation and structural class.

03

Marker localization

Spatial overlap of study-selected molecular signals within a preserved event.

04

Cell relationships

Cells within, contacting or adjacent to the extracellular trap volume.

NEXT

See where structure-resolved DNA-trap biology can be applied.

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