# Bioparticle — Full Website Content

> Bioparticle is the official channel partner for the field's most sensitive nanoparticle platforms. We supply the instruments and reagents that resolve the size, charge, and surface markers of biological nanoparticles — down to a single molecule, with no calibration curves — for extracellular vesicle (EV), lipid nanoparticle (LNP), virus/VLP, nanobubble, and antibody research.

This document contains the complete content of bioparticle.com so an AI assistant can accurately answer questions about the company, its products, and its services.

## Company facts

- **Name:** Bioparticle
- **Tagline:** Accelerating the particle research of life — "Characterize the particles other instruments can't see."
- **What we do:** Official channel partner for the most sensitive nanoparticle instruments and reagents. Bioparticle brings the instruments and reagents that resolve the size, charge, and surface markers of biological nanoparticles — down to a single molecule, with no calibration curves and no compromises — to your lab.
- **Products:** Pangnostics dFC (single-molecule digital flow cytometry); ZetaView Evolution by Particle Metrix (multiparameter nanoparticle tracking analysis); Lyophilized Exosomes (EV reference standard); F-NTA Antibodies (fluorescence-NTA tetraspanin reagents).
- **Services:** Scientific consulting; MedTech quality & regulatory; digital transformation (Odoo ERP); engineering & product development — delivered through a Bioparticle × Unplex® partnership.
- **Email:** info@bioparticle.com
- **Phone:** +1 (480) 604-5662
- **Address:** 2820 N Torino Avenue, Tucson, Arizona 85712, USA
- **Regulatory status:** All instruments and reagents are For Research Use Only. Not for use in diagnostic procedures.
- **Website:** https://bioparticle.com

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## Brand

**Name:** Bioparticle (styled lowercase as "bioparticle" in the wordmark).

**Mission / positioning:** Accelerating the particle research of life.

**Taglines & key messages:**
- "Characterize the particles other instruments can't see."
- Official channel partner for the field's most sensitive nanoparticle platforms.
- Absolute, calibration-free measurement — no calibration curves, no compromises.
- Down to a single molecule.

**Logo:** A lowercase "bioparticle" wordmark paired with a particle mark — a small cluster of green dots representing nanoparticles. Files: `/logo.svg` (vector) and `/assets/bioparticle-logo.png` (raster).

**Voice & tone:** Scientific, precise, confident, and clear. Explains complex nanoparticle measurement in plain, credible language; grounded in physics and reproducibility; avoids hype.

### Typography

- **Display / headings:** Spectral (serif) — used for headlines, set in regular/light weight with tight letter-spacing.
- **Body text:** IBM Plex Sans.
- **Labels, eyebrows, data read-outs, captions:** IBM Plex Mono (uppercase, letter-spaced).

### Brand colours

**Green — primary brand colour**
- `#1FA64E` — primary brand green (CTAs, accents, logo mark)
- `#137A38` — dark green (headings, hovers)
- `#EAF6EE` — light green tint (backgrounds)

**Gold / amber — secondary accent**
- `#C99A2E` — gold
- `#8C6610` — dark gold
- `#FAF2DB` — light gold tint
- `#E0B23C` — soft amber

**Neutrals & surfaces**
- `#F5F7F4` — porcelain (page background)
- `#FCFDFB` — paper (cards / panels)
- `#16201C` — ink (primary text, dark buttons)
- `#37463F` — charcoal (dark sections, secondary text)
- `#5C6862` — muted text
- `#E2E6E1` — line (borders / hairlines)
- `#FFFFFF` — white

**Fluorescence channel colours (tetraspanin markers)** — used consistently across product illustrations:
- CD9: `#1FA64E` (green · 488 nm channel)
- CD63: `#E08A1E` (orange · 561 nm channel)
- CD81: `#7A5AF8` (violet · 640 nm channel)

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## Home — https://bioparticle.com/

**Headline:** Characterize the particles other instruments can't see.

As the official channel partner for the field's most sensitive nanoparticle platforms, Bioparticle brings the instruments and reagents that resolve the size, charge, and surface markers of biological nanoparticles — down to a single molecule, with no calibration curves and no compromises — to your lab.

### Two platforms

**Particle Metrix · ZetaView — Next-Generation Particle Characterization Platform.** The ZetaView evaluation platform integrates cutting-edge detection modules for complete biological particle analysis. Designed for reliability, reproducibility, and simplicity, it eliminates manual calibration and provides real-time quantitative data.
- Measure size, concentration, zeta potential, and fluorescence simultaneously.
- Adaptive sample scanning for unknown particle compositions.
- High-sensitivity optics with automated parameter control.
- Data you can trust — every scan, every sample.

**Pangnostics · Digital Flow Cytometry — Next-Generation Platform.** Pangnostics delivers a breakthrough in particle analysis, bringing single-molecule precision to complex biological systems. By overcoming the detection limits of conventional cytometry, it uncovers hidden subpopulations and generates truly quantitative insights.
- Ultra-sensitive detection down to single molecules.
- Expose hidden nanoparticle populations beyond traditional limits.
- High-dimensional phenotyping with expandable multi-color architecture.
- Direct digital counting — no calibration curves, no compromises.

### Inside the instruments — two ways of seeing the nanoscale

These platforms read biological particles through complementary physics — tracking how particles move, and characterizing the single molecules on their surface.

**Nanoparticle Tracking Analysis (Particle Metrix ZetaView).** Up to four lasers illuminate the particles suspended in the cell, while a camera records the light each one scatters — and the fluorescence from labelled particles — as they move under Brownian motion. The Stokes–Einstein relation converts that motion into a hydrodynamic diameter, and counting the tracked particles in a known volume gives an absolute concentration — particle by particle, no calibration curve required. Tracking → size & concentration; Electrophoresis → zeta potential; F-NTA → fluorescence.

**Digital Flow Cytometry (Pangnostics dFC).** Sample flows through a planar microfluidic channel where line-confocal optics and four lasers interrogate a tiny detection volume. Each fluorophore-tagged molecule is counted as it passes — across twelve channels — giving absolute, calibration-free numbers and per-particle phenotypes that bulk methods average away. Count → absolute concentration; Colocalize → multiplex phenotype; Copies/particle → surface density.

### How the methods compare — most of the EV population hides below the floor

Therapeutic and biofluid preparations are dominated by 30–70 nm vesicles. Where a method's detection floor sits decides whether you measure the real sample — or a brighter, biased subset of it.

| Method | Smallest particle | Label-free size | Per-particle | Absolute count | Copies/particle |
|---|---|---|---|---|---|
| Western blot / ELISA | bulk (no sizing) | — | ✕ | ✕ | ✕ |
| Conventional flow | ~500 nm | ✕ | ✓ | relative | ✕ |
| High-sensitivity flow | ~70–80 nm | ✕ | ✓ | bead-calibrated | semi |
| Nanoparticle tracking (NTA) | ~10 nm | ✓ | ✓ | ✓ | ✕ |
| Single-molecule dFC | ~1 nm | fluorescence | ✓ | ✓ calibration-free | ✓ |

### The measurement evolution — from bulk averages to single molecules

1. **Bulk averaging** — Western blot & ELISA confirm a marker is present, but only as a population average.
2. **Particle tracking** — NTA reads Brownian motion for label-free size, concentration, and zeta, particle by particle.
3. **Single-EV phenotyping** — high-sensitivity flow resolves markers on individual vesicles, but a detection floor still hides the smallest EVs.
4. **Single-molecule digital (now)** — Pangnostics dFC counts individual molecules to ≤35 nm — absolute, calibration-free, with copies-per-particle.

### Applications (nanoparticles in biology)

- **Extracellular Vesicles** — size, concentration, and surface markers, with per-EV phenotyping.
- **Lipid Nanoparticles** — LNP analysis for drug delivery and mRNA therapeutics.
- **Nanobubbles** — size, charge, and stability across diverse media.
- **Viruses & VLPs** — characterisation for diagnostics and vaccine development.
- **Environmental** — tracking nanoparticles for ecological impact studies.

### Portfolio

- Pangnostics dFC — single-molecule digital flow cytometry.
- ZetaView Evolution — multiparameter NTA.
- Lyophilized Exosomes — reference material for calibration and method development.
- F-NTA Antibodies — CD9/CD63/CD81 tetraspanin detection antibodies.
- Method Qualification (Services) — scientific, regulatory, and engineering support.

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## Pangnostics dFC — https://bioparticle.com/pangnostics

**Headline:** See the 90% your cytometer is missing.

The Pangnostics dFC is an ultra-high-sensitivity single-molecule counter in a familiar flow-cytometry format — counting, sizing, and phenotyping every extracellular vesicle, LNP, viral vector, and antibody that flows through, without a single calibration bead.

**Key numbers:** ~100% single-molecule detection efficiency · 4 lasers × 12 detection channels · 1–96 samples per run · 0 standard curves required.

### Why it matters

For decades, flow cytometry has driven our understanding of cellular heterogeneity. But when the same instruments are turned on the nanoscale — extracellular vesicles, lipid nanoparticles, viral vectors — a large fraction of every sample stays hidden below the instrument's detection floor. Most EVs are smaller than 70 nm and dimmer than a handful of fluorophores, so they simply aren't counted. Every downstream conclusion inherits that blind spot.

Pangnostics dFC closes the gap with a fundamentally different optical design: planar microfluidics and line-confocal detection that count individual fluorophore-tagged molecules directly, with essentially 100% single-molecule detection efficiency. The result is absolute, calibration-free quantitation — and a per-particle view of size, surface markers, and copy number that bulk methods average away.

### How digital flow cytometry works (four steps)

1. **Flow** — A 10 µL sample is drawn into a planar microfluidic chip and flows single-file through a detection channel just a couple of micrometres across, so particles pass the laser one at a time. (Planar microfluidics · ~2 µm detection channel.)
2. **Illuminate** — Four spatially separated lasers (405, 488, 561 and 637 nm) are shaped into a line-confocal light sheet spanning the channel, defining a tiny, evenly-lit detection volume every particle must cross. (4 lasers · line-confocal light-sheet detection.)
3. **Count** — Each fluorophore that crosses the sheet emits a burst of photons recorded by single-photon detectors. Bursts above a noise threshold are counted as individual molecules, with essentially 100% detection efficiency and a very low false-positive rate. (Direct single-molecule counting · ~100% efficiency.)
4. **Phenotype** — Twelve channels read the bursts across up to eighteen dyes at once. Colocalizing signals on the same particle gives a true multi-parameter phenotype — and the copy number of each marker, per vesicle. (12 channels · multiplex colocalization · copies/particle.)

### Key capabilities — six things bulk methods can't do

- **Single-molecule sensitivity** — validated detection efficiency near 100% across more than 30 fluorescent dyes. Every photon-emitting molecule is counted — including the dimmest — not estimated from a curve.
- **High-plex phenotyping** — four lasers and twelve simultaneous channels resolve surface-marker combinations on individual nanoparticles in a single run; expandable for higher-plex assays.
- **Absolute quantitation** — direct digital counting yields true concentrations and biomarker copy numbers — no calibration beads, no reference ladders, no ~20% bead-calibration uncertainty.
- **Flexible throughput** — run a single urgent sample or a full 96-well plate on the same platform, with a familiar flow-cytometry workflow and no specialist operator required.
- **Reveals heterogeneity** — surfaces the dim, small, and rare subpopulations (well under 1% of total particles) that bulk and commercial high-sensitivity platforms miss by design.
- **Reagent authentication built in** — measures the absolute concentration of antibody-dye conjugates that can't be read at 280 nm, plus dye-to-protein ratio, removing lot-to-lot reagent variability as a source of irreproducibility.

### Applications

- **Extracellular vesicles & exosomes** — phenotype individual EVs across twelve colors; quantify tetraspanin and engineered-marker copy number and absolute subpopulation concentration for liquid biopsy and EV therapeutics.
- **Lipid nanoparticles (LNPs)** — characterize mRNA and gene-therapy LNPs at the single-particle level: payload distribution, surface composition, and encapsulation uniformity.
- **AAV & viral vectors** — distinguish full, empty, and partial capsids; measure titer and payload heterogeneity for vector development and release characterization.
- **Protein aggregates & complexes** — resolve oligomeric states and RNA-binding protein complexes that bulk methods cannot separate from vesicular populations.
- **Analytical & therapeutic antibodies** — authenticate dye-to-protein ratios, quantify aggregation, and verify conjugate concentration.
- **Nanoparticle standardization** — reference-grade absolute concentrations make dFC an orthogonal method for cross-laboratory harmonization and reagent QC.

### Rigor & reproducibility

Absolute counting removes the calibration drift, curve-fitting, and vendor-dependent reagent variability that compromise quantitative EV flow cytometry. Copy-number and sizing methods have been validated against orthogonal techniques including super-resolution and single-molecule TIRF microscopy, and the platform is designed to support standardized community reporting. Aligned with MISEV2023 reporting and the MIFlowCyt-EV framework; orthogonally validated against super-resolution / TIRF; ~4 orders of magnitude dynamic range.

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## ZetaView Evolution (Particle Metrix) — https://bioparticle.com/zetaview

**Headline:** Watch each particle move, and read its size, charge, and markers.

ZetaView Evolution tracks thousands of individual nanoparticles in real time — turning Brownian motion into hydrodynamic size, a whole-cell scan into absolute concentration, an applied field into zeta potential, and fluorescent labels into specificity. One instrument, six measurements, no calibration curves.

**Key numbers:** 10–1000 nm particle size range · 6 measurements from one cell · 4 excitation lasers, up to 11 channels · 0 calibration curves.

### The instrument — one bench-top platform, every measurement

Up to four excitation lasers, a high-sensitivity CMOS camera, and a quartz-glass measurement cell work together under ZetaSphere® software — so size, concentration, zeta potential, fluorescence, and colocalization all come from the same particles, in a single run.

**Inside the platform:**
- Up to four excitation lasers — selected from 405 / 488 / 520 / 640 / 660 nm, doubling as scatter and fluorescence sources.
- High-sensitivity CMOS camera — records the light each particle scatters, and its fluorescence, particle by particle.
- Quartz-glass measurement cell — zeta potential measured directly inside the cell, with no disposables.
- ZetaSphere® software — one-click multiparameter acquisition, live statistics, and full sample reporting.
- Configurations: Mono (1 laser) · Twin (2) · Quatt (4) · up to 11 fluorescence channels · Made in Germany.

### Six measurements, one sample

Nanoparticle tracking analysis follows particles one at a time rather than averaging the whole suspension. That single difference lets ZetaView resolve a polydisperse sample into its true size distribution, count particles in absolute terms, measure their surface charge, and separate a genuine subpopulation from background.

- **Particle size distribution** — Brownian motion is faster for small particles and slower for large ones. The Stokes–Einstein relation converts each tracked path into a hydrodynamic diameter, and thousands of particles build a full distribution — not a single average (reports D10 / D50 / D90 and span).
- **Concentration Scanning Technology** — ZetaView Evolution sweeps the laser through the entire measurement cell, illuminating each plane in turn and capturing every particle it crosses. Counting the whole volume yields an absolute, calibration-free concentration that stays comparable across sample types and across scatter and fluorescence channels, independent of camera gain or laser intensity.
- **Zeta potential** — apply an electric field and charged particles migrate; their velocity reveals the zeta potential, the effective surface charge that governs colloidal stability. Measured in the same cell, on the same particles just sized. Range −500 to +500 mV, pH 1–13.
- **Fluorescence detection (F-NTA)** — light scatter sees every particle; add a fluorescent label and ZetaView counts only what carries your marker, separating specific signal from noisy background in the same sample.
- **Colocalization analysis (C-NTA)** — two labels, two lasers. ZetaView detects each particle in both fluorescence channels and resolves the population into CD9-positive, CD63-positive, and colocalized double-positive vesicles. C-NTA needs at least two lasers (Twin and Quatt configurations).
- **Subpopulation analysis** — resolving a subpopulation by size, zeta potential, and fluorescence together isolates a genuine subset and reports its count, fraction, and characteristic size, separating a true EV subset from background that any single parameter would blur.

### Applications

- Extracellular vesicles — size, concentration, and tetraspanin profiling with per-EV fluorescence.
- Lipid nanoparticles — size and zeta for LNP stability in mRNA and gene-delivery work.
- Viruses & VLPs — titre, integrity, and stability for diagnostics and vaccine development.
- Biopharma QC — lot-to-lot consistency and stability studies for GLP/GMP workflows.

### Why ZetaView

- **Widely cited platform** — an NTA system established across peer-reviewed EV, virus, and nanomedicine literature. Adopted by research groups and biopharma teams worldwide (users include Medical University of Vienna, Masaryk University, Ludwig Boltzmann Institute for Traumatology, and Steinbeis).
- **One cell, one workflow** — size, concentration, zeta, fluorescence, and colocalization on the same particles, no instrument-hopping.
- **Data integrity built in** — ZetaSphere® logs database events and predefined settings for reproducible, auditable multiparameter workflows.

### Specifications

- **Size range:** 10 – 1000 nm (sample and laser dependent)
- **Concentration:** 10⁵ – 10⁹ particles/mL · calibration-free Concentration Scanning Technology
- **Zeta potential:** −500 to +500 mV · measured directly in the quartz-glass cell, no disposables · pH 1–13
- **Fluorescence:** up to four lasers (405 / 488 / 520 / 640 / 660 nm) · up to 11 channels · sensitivity < 20 AF488 molecules
- **Parameters:** size · concentration · zeta · fluorescence (F-NTA) · colocalization (C-NTA)
- **Software:** ZetaSphere® — one-click multiparameter acquisition, live statistics, reporting
- **Configurations:** Mono (1 laser) · Twin (2) · Quatt (4) · Made in Germany

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## Lyophilized Exosomes — https://bioparticle.com/exosomes

**Headline:** A known sample, so you can trust the unknown ones.

Lyophilized Exosomes are stable, extensively characterized biological particles — positive controls and calibration standards derived from traceable human cell lines. Reconstitute, measure, and benchmark your instrument against a value you can rely on, with no cold chain required.

**Key numbers:** source-verified from traceable human cell lines · 4 characterized attributes (size, concentration, markers, morphology) · no cold chain (lyophilized stability) · lot-to-lot batch consistency.

### Why a reference standard

NTA gives absolute, calibration-free numbers — but to trust those numbers over time, across operators, and between sites, you need a stable sample of known properties to measure against. A well-characterized EV standard is that anchor: it tells you whether a shift in your data is real biology or instrument drift. Because these exosomes are lyophilized, each vial is shelf-stable and ships without cold-chain logistics — the same lot can benchmark an instrument today and a year from now.

Benchmarking in action: run the standard repeatedly and plot each result against its certified value. Points inside the ±2σ band mean the instrument is in control; a systematic shift pushes them past the limits, flagging drift before it reaches your real samples.

### What you get — one standard, four (plus) jobs

- **Cross-site validation** — confirm instrument performance across multiple sites and timepoints with a common reference.
- **Assay reproducibility** — build reproducibility into EV assays and diagnostic workflows from the start.
- **Operator onboarding** — a reliable standard for training lab staff and students on consistent technique.
- **QC validation packages** — support QC validation in pre-clinical and commercial pipelines.
- **Tested every lot** — each lot tested for size, concentration, protein markers, and morphology.
- **Lyophilized format** — long-term stability without cold-chain logistics.

### Used across

- Extracellular vesicles — subpopulation tracking using CD9 / CD63 / CD81 markers.
- Virology — confirm viral capsid protein presence in particle populations.
- Nanomedicine — validate surface modifications of lipid or polymer nanoparticles.
- Method validation — anchor instrument qualification and stability studies.

### Reference standard details

- **Source:** traceable, ethically sourced human cell lines
- **Format:** lyophilized — reconstitutable, shelf-stable, no cold chain
- **Characterization:** per-lot testing of size, concentration, protein markers, and morphology
- **Markers:** tetraspanin-positive (CD9 / CD63 / CD81) for subpopulation work
- **Use:** positive control & calibration standard for NTA and EV assays

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## F-NTA Antibodies — https://bioparticle.com/fnta-antibodies

**Headline:** Turn a particle count into a specific one.

Fluorescence-NTA earns its specificity from the label. These antibodies are optimized for the ZetaView® platform — ready-to-use, lyophilized for shelf stability, and targeted to the EV surface markers that tell your vesicles apart from everything else in the sample.

**Key numbers:** 3 markers (CD9 · CD63 · CD81) · 1 tetraspanin cocktail kit · 1 IgG isotype control · ready-to-use with minimal prep.

### Why F-NTA reagents — specificity is a reagent decision

Light scatter counts every particle in a suspension; fluorescence counts only the ones your antibody binds. The quality of that distinction — the gap between total and specific — depends entirely on the label: its affinity, its fluorophore, and the control you run alongside it. Each antibody here is high-affinity and lyophilized for lot-to-lot consistency, with an IgG isotype control so you can measure and subtract non-specific background instead of guessing at it.

### The reagents (catalog) — five products, one F-NTA workflow

- **F-NTA CD9** (detection antibody) — high-affinity CD9 detection antibody for tetraspanin-positive EV subpopulations. CD9 · 488 nm channel.
- **F-NTA CD63** (detection antibody) — CD63 detection antibody for resolving the CD63-positive vesicle fraction. CD63 · 561 nm channel.
- **F-NTA CD81** (detection antibody) — CD81 detection antibody for the third canonical EV tetraspanin marker. CD81 · 640 nm channel.
- **F-NTA EV Tetraspanin Kit** (detection kit) — a ready-to-use cocktail for broad tetraspanin coverage across CD9, CD63, and CD81. Multi-marker coverage.
- **F-NTA IgG Control** (control) — isotype control antibody to quantify and subtract non-specific background signal. Negative reference.

### Why these reagents

- **High specificity** — targeted to EV surface markers (CD9, CD63, CD81) and viral proteins.
- **Ready-to-use** — minimal preparation time, optimized for the ZetaView platform.
- **Lyophilized** — long shelf life and consistent lot-to-lot reproducibility.
- **Marker-to-count** — correlate surface biomarker expression directly with particle counts.
- **Broad research utility** — EV biology, vaccine development, and nanoparticle targeting studies.
- **QC & release** — supports validated assays for release testing in regulated settings.

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## Services — https://bioparticle.com/services

**Headline:** Expertise that moves you from idea to compliant product.

Bioparticle has partnered with Unplex® to bring a powerful trio of services to medtech and biotech innovators — combining scientific depth in nanoparticles, regulatory rigor, digital systems, and engineering under one roof.

### 1. Scientific consulting — expertise in EVs, nanoparticles, nanobubbles & VLPs

Accelerate discovery, streamline analytics, and scale production for biological and synthetic nanoparticles.
- Workflow design & feasibility — isolation, purification, characterization.
- Process development & scale-up from bench to pilot and GMP.
- Characterization & analytical strategy across NTA, flow, and microscopy.
- Regulatory & quality readiness aligned to cGMP expectations.
- Commercialization & partnership strategy.

### 2. MedTech quality & regulatory — navigate compliance with confidence

Deep regulatory expertise so your innovations meet global standards — from ISO 13485 to FDA 21 CFR Part 820 and MDR.
- QMS implementation & auditing (ISO 13485, FDA, MDR).
- IEC 62304 software lifecycle & technical documentation.
- Technical file creation & regulatory submissions.
- Risk management and usability engineering.
- Regulatory strategy for international markets (FDA, CE).

### 3. Digital transformation — unify operations with Odoo ERP

Customized Odoo ERP implementations for growing medtech and biotech companies.
- Custom Odoo ERP setup & module development.
- Integration with R&D, QA/RA, and supply-chain workflows.
- Secure data management and document traceability.
- Ongoing support and training.

### 4. Engineering & product development — concept to pilot production (nine stages)

Unplex® brings deep-tech product development across the full lifecycle, applied to life-science instrumentation and diagnostics.
1. **Industrial Design** — concept sketches and form studies; ergonomics and bench footprint; brand-aligned enclosure and finish.
2. **System Design** — requirements capture and architecture; interface and data-flow definition; feasibility and trade-off analysis.
3. **Hardware Design** — analog and digital board design; sensor and detector integration; low-noise signal acquisition.
4. **Mechanical Design** — optical and fluidic alignment; tolerance and thermal management; design-for-manufacture CAD.
5. **Software** — embedded firmware and control; acquisition and analysis pipelines; audit-ready data and clear UX.
6. **Sourcing** — vendor qualification; lead-time and BOM management; logistics and supply continuity.
7. **Prototyping** — rapid functional prototypes; system integration and bring-up; design iteration on real data.
8. **Compliance** — ISO 13485 and IEC 62304 alignment; risk management and usability; verification and validation.
9. **Pilot Production** — pilot-run setup and DFM; process and assembly documentation; a clear path to volume manufacturing.

### Who we support

- Academic and translational research labs.
- Biotech and biopharma companies.
- CROs and CDMOs working with EVs, LNPs, viruses, or VLPs.

### The partnership

Unplex® is a deep-tech product development and manufacturing partner spanning medical devices, defense, and industrial automation — with teams in Tucson, Bengaluru, and Ontario. (https://unplex.tech)

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## Contact — https://bioparticle.com/contact

Tell us about your sample, your target, or your project — whether it's an instrument, a reagent, a reference standard, or a method question, we'll point you to the right answer.

- **Email:** info@bioparticle.com
- **Phone:** +1 (480) 604-5662
- **Address:** 2820 N Torino Avenue, Tucson, Arizona 85712, USA
- A contact form is available on the page (first name, last name, email, subject, message).

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For Research Use Only. Not for use in diagnostic procedures. © Bioparticle.