Our Services

Antibody Innovation & Diagnostic Platform Development

At VexisBio Inc., we specialize in application-driven antibody discovery and translational in vitro diagnostic (IVD) development.

Our platform bridges biomarker science and commercial diagnostic execution — enabling biotech innovators to convert biological insight into scalable diagnostic solutions.

We focus on three integrated pillars:

• Antibody Discovery & Engineering
• Immunoassay & Biomarker Development
• IVD Kit Development & Commercialization Support


1. Antibody Discovery & Engineering

High-performance diagnostics begin with high-quality antibodies.

We develop antibodies engineered specifically for diagnostic applications, including ELISA and multiplex assay formats.

Capabilities

  • Antigen design (protein, peptide, small molecule conjugates)
  • Recombinant antigen production
  • Hybridoma development
  • Phage display screening
  • High-affinity monoclonal antibody generation
  • Epitope mapping & binning
  • Antibody pair screening for sandwich ELISA
  • Cross-reactivity testing
  • Affinity ranking & optimization
  • Scalable antibody production

Our screening strategy prioritizes assay performance, not just binding affinity.


2. Biomarker & Immunoassay Development

We transform validated antibodies into high-sensitivity, reproducible immunoassays designed for translational and commercial deployment.

Assay Development Services

  • Custom sandwich ELISA development
  • Competitive ELISA design
  • Multiplex biomarker panels
  • Low-abundance protein detection
  • Cytokine and growth factor quantification
  • Matrix compatibility optimization (serum, plasma, CSF)
  • Signal-to-noise optimization
  • Blocking and buffer refinement

Analytical Validation

  • Limit of detection (LOD)
  • Limit of quantification (LOQ)
  • Linearity and dynamic range
  • Precision (intra/inter assay)
  • Specificity and cross-reactivity testing
  • Reproducibility studies

Our development strategy integrates assay robustness and scalability from the earliest stages.


3. IVD Kit Development & Commercialization Support

We bridge the gap between functional assay and market-ready diagnostic kit.

Diagnostic Kit Development

  • Assay-to-kit translation
  • Reagent formulation optimization
  • Antibody stabilization strategies
  • Calibrator and control development
  • Plate coating optimization
  • Packaging configuration
  • Accelerated stability studies
  • Lot-to-lot consistency validation

OEM & Scale-Up Support

  • White-label kit development
  • Bulk antibody supply
  • Process documentation support
  • Technology transfer planning
  • Long-term manufacturing alignment

Our focus is diagnostic-ready performance and scalable product design.


4. Neurodegenerative & Oncology Focus Areas

We support biomarker development programs in:

Neurodegenerative Diseases

  • Alzheimer’s disease biomarkers
  • Tau and amyloid-related targets
  • Neurofilament light chain (NfL)
  • Neuroinflammation markers

Oncology

  • Tumor-associated antigens
  • Cytokine panels
  • Translational biomarker validation
  • Companion diagnostic assay development

Inflammatory & Immune Profiling

  • Growth factor quantification
  • Immune activation panels
  • Cytokine detection systems

5. Development Pathways

We structure projects based on stage and goals:

Feasibility Programs

Rapid biomarker and antibody performance validation.

Assay Development Programs

Comprehensive antibody pair screening and analytical optimization.

IVD Commercialization Programs

From validated assay to scalable diagnostic kit prototype.


Why Partner with VexisBio?

✔ Application-Driven Antibody Engineering
✔ Integrated Antibody-to-Kit Development
✔ Diagnostic-Focused Optimization
✔ Flexible Development Models
✔ Located in the San Diego Biotech Ecosystem

We operate as a strategic development partner — aligning antibody discovery with translational and commercial success.

Biotech Services at a Glance

Transparent pricing, ISO-styled QC, quick turnarounds (Request a quote).

Service Tables

Scope Typical Turnaround Price (USD)
ELISA feasibility (pairing + LoD check) 2–4 weeks $3,000–$5,000
Antibody pairing/screening (existing clones) 1–3 weeks $2,000–$6,000 / target
Antibody Discovery 4-6 Months Start from $30,000
Assay optimization (linearity, precision) 2–4 weeks $4,000–$8,000
Tech transfer (SOPs, layout, QC plan) 1–2 weeks $5,000–$8,000

Antibody Work

Scope Typical Turnaround Price (USD)
Custom antibody development (RUO) 10–14 weeks $15,000–$22,000
Conjugation pilot (1 label: HRP/biotin/fluor/gold/Eu/oligo)  1–2 weeks $2,000+
Scale conjugation (2–5 mg input) + report 1–2 weeks $1,800–$3,500 / lot
Extra label on same clone + $400–$700
Customer-supplied antibody QC intake $150 / vial

Recombinant Proteins (E. coli)

Scope Typical Turnaround Price (USD)
Cloning into provided vector 3-7 business days $800–$1,200
Expression screen (3–6 conditions) 1–2 weeks $1,200-$2,000
Purification (affinity± polish) 3-7 business days $800–$1,500 / run
Polishing (IEX/SEC) add-on Per step + $300–$600
Endotoxin reduction workflow Per lot + $250–$600
QC add-ons (BCA/HPLC/MS as available) Per test $100–$600

Nucleic Acid & Endotoxin

Scope Typical Turnaround Price (USD)
DNA/RNA extraction (mini-batch ≤ 12) 3–5 business days $35–$85 / sample
Plasmid prep (Mini/Midi/Maxi) 2–5 business days $60 / $180 / $350
Endotoxin-low plasmid option + $60-$120 / prep
LAL endotoxin test (gel-clot/kinetic) 2-3 business days $150 / sample (5–19: $120; 20+: $100)

Packaging, OEM & Consulting

Scope Typical Turnaround Price (USD)
OEM/white-label fill/finish (RUO) Per lot $400–$900 + materials
Label/COA generation (per SKU) $120-$240
Scientific consulting / method review As scheduled $150 / hr
Custom bench work (outside bundles) As scheduled $120-$160 / hr + consumables

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Notes

  • Usage: RUO only. Not for diagnostic use.
  • Rush Service: Turnarounds reflect typical queues; rush service +15–25% if available.
  • Logistics: Intake & logistics (receiving/biorepository) $50–$120 per shipment when applicable.
  • Project Workflow: Multi-phase projects run Feasibility → Optimization → Scale-up → Tech transfer with QC gates.

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