Living channels.
Programmable flow.

The first self-assembling, optogenetically controlled microfluidic platform. No cleanroom required.

10,440 KO pairs screened 100× dynamic range <$1 per device 18 months to prototype

Microfluidics is stuck in the cleanroom.

Every experiment starts with a photomask and weeks of fabrication. Biology moved on — microfluidics hasn't.

01

2–4 weeks per chip, $5k–$20k per mask

PDMS fabrication requires a cleanroom. Each design change means a new photomask — slow iteration, high cost, high barrier to entry.

02

Passive channels — no programmability

Active valves require complex external pneumatic systems. No built-in actuation. No design reusability across projects.

03

Single-use waste — clogging kills the chip

Channel fouling is terminal. Each clog means discarding the device and restarting fabrication from scratch.

$25B

Microfluidics market by 2028 — growth limited by fabrication bottlenecks and passive chip designs.

Every experiment starts with a cleanroom. Biology moved on — microfluidics hasn't.

One fungus. One week. Zero cleanroom.

Sivoro replaces photolithography with engineered fungi that self-assemble into precision microfluidic channels.

Feature Sivoro Living Chip Conventional PDMS
Fabrication Fungus grows channels Photolithography (cleanroom)
Valves Light-controlled (450 nm, built-in) Pneumatic pumps (external)
Iteration Days (transform strain) Weeks (redesign mask)
Channel fouling Self-clearing (hyphal turnover) Terminal (chip disposal)
Per-device cost <$1 (after strain) $50–$500

Three layers of proprietary IP

From metabolic chassis to optogenetic valve to physical scaffold — each layer independently defensible.

Layer 1 — Chassis

Metabolically Orthogonal N. crassa

Engineered to eat xylose only — cannot metabolize glucose, amino acids, or organic acids present in lab reagents. Six-gene knockout validated in silico from 10,440 combinations screened.

Composition of matter Screening method

Layer 2 — Valve

Optogenetic Septal Pore Valve

Blue light (450 nm) triggers pore closure. 100× dynamic range between dark and lit states. LOV2-Jα-HEX1 fusion protein + SPA1-ePDZ pore-rim anchor.

Optogenetic construct Flow control method

Layer 3 — Scaffold

H-Tree Scaffold & Integration

Parametric design (10×10 mm, 16 ports). Compatible with SU-8/PDMS or direct printing. Channel dimensions engineered for 2–8 hyphae (13–20 µm width, 15 µm depth).

Fungal-specific geometry Co-culture methods

65% complete —
all computational phases done

"We are one wet-lab milestone away from a functional prototype."

View Full Milestone Plan →
Metabolic Modeling 100%
KO Screen (10,440 pairs) 100%
Optogenetic Valve Design 100%
Chip Scaffold Design 100%
Wet-Lab Validation Next →

The only living, self-assembling microfluidic platform

Sivoro occupies a unique position: simple fabrication, active biological control. No competitor is in this quadrant.

Competitor Sivoro Advantage
Emulate, Inc.No living channels; $200k+ instruments
CN Bio InnovationsLower cost, faster iteration
MicronitNo cleanroom required
Fluidigm / Standard BioTools10× lower price; biological actuation

X axis: Active control · Y axis: Fabrication simplicity

Computational validation complete

0

Knockout pairs screened in silico

0

Validated optogenetic constructs

0

pLDDT — LOV2 domain (ColabFold)

0

pLDDT — HEX1 domain (ColabFold)

0

Patent families ready to file

0+

Lines of Python modeling code

IP Status

Provisional draft complete · 5 claim families · ready to file within 30 days of legal engagement

$1.5M

18 months runway to prototype + first sale

Seed

Round

$6M

Pre-money

$7.5M

Post-money

18 mo

Runway

"We are one wet-lab milestone away from a functional prototype — exactly what this seed round funds."
View Investor Materials → Download Pitch Deck