Biomanufacturing / CDMO Service Information:
Cell Culture Capabilities:
- Up to 100 L and beyond, depending on project
Quality Control Testing:- Manufactured in a United States-based facility with qualified personnel and calibrated/maintained instrumentation. Head of Quality will assist customers with process documentation transfer for potential GMP manufacture, if required.
Fully executed COA includes:
- Purity ≥ 90%
- Aggregation ≤ 5%
- Endotoxin levels ≤ 2 EU/mg
- Functionality testing by ELISA
- Screen for adventitious agents (Impact Assay)
End Uses:
Therapeutic:- Biological Proof of Principle (POP) Studies
- Toxicology Studies
- Pharmcokinetic (PK) Studies Studies
- Pharmacodynamic (PD) Studies
- Animal Efficacy Studies
- In Vitro & Cell-Based Assays
Diagnostic:- Enzyme Immunosorbant Assay (EIA)
- Lateral Flow Assay or Immunoassay
- ELISA Assay
- Immunohistochemistry (IHC)
- Immunoprecipitation (IP)
- Western Blot (WB)
- Antibody Pairing
- IF/Flow cytometry
- Anti-Idiotypic (Anti-ID; Anti-Idiotype) Antibody
- Anti-Drug Antibody (ADA)
- Phosphorylation-Specific Antibody
- G protein-coupled receptors (GPCRs)
Other:- Protein Antigen Production
- Antigen-Specific Reagent (ASR)
- Laboratory-Developed Test (LDT)
- Research Use Only Reagent (RUO)