Duoning 2023 Product Catalog for Bioprocess Platform

A 2023 product catalog from Duoning Bio featuring serum-free media, bioreactors, filtration systems, and validation services for biopharmaceutical…


Duoning 2023 Product Catalog for Bioprocess Platform - cover page
Brand
Duoning
Category
Other
Document type
Product Leaflet
Language
Chinese
Pages
40
File format
PDF
File size
1.2 MB
Published
23 October, 2026
Updated
23 October, 2026
MD5 checksum
EB7B43DB3B1E620A12848FE776259677

About this manual

Duoning Bio is a leading provider of one-stop bioprocess solutions in China, offering comprehensive services from upstream cell culture media and bioreactors to downstream filtration, chromatography, and filling. The company operates two main business lines: bioprocess solutions and laboratory products and services, aiming to help partners achieve efficient, stable, and cost-controlled drug development and production processes. This manual is written in Chinese.

What's inside

  • Serum-Free Media
  • Feed Media
  • Cell Culture Flasks
  • Bioreactors
  • One-Time Solutions
  • Laboratory Equipment
  • Filtration
  • Reagents
  • Adsorbents
  • Compliance Verification Services

Specifications

Total Volume500 mL
Working Volume100-350 mL
Temperature Control Accuracy±0.1°C
Air Flow Range0-100 ml /min
CO2 Flow Range0-50 ml /min
Dissolved Oxygen Control Range0~200%
pH Range2.0~12.0
Stirring Speed Range0-300rpm

Frequently asked questions

What is the main advantage of serum-free media?

Serum-free media eliminates animal-derived components and ensures batch-to-batch consistency with chemically defined nutrients.

Which cells are suitable for Media C media?

Media C is suitable for CHO-K1, CHO-S, DG44, and CHOK1SV cell lines using GS and dhfr selection systems.

What is the capacity of the DuoBioTM Explore series bioreactors?

The DuoBioTM Explore series bioreactors have a total volume of 500 mL with a working volume of 100-350 mL.

Does the DuoBioTM Explore series comply with FDA regulations?

Yes, the system complies with GMP and FDA 21 CFR Part 11 requirements.

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