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Bio-macromolecular Drugs Products
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HEK293 Series Culture Medium
HEK293 CDM26 Pro

HEK293 CDM26 Pro

Application:

  • Antibody production
  • Vaccine production
  • Technical support
  • Contact us
No. Specification Form Price(CNY)
LQ26-2 500mL,1000mL Liquid(LQ)

Price 500.00/LYour price
Contact us to get exclusive rates for you

DP26-2 10L,50L,100L Dry Powder(DP)

Price 300.00/LYour price
Contact us to get exclusive rates for you

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  • Product overview
  • Application
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Product overview

HEK293 CDM26 Pro is chemically-defined (CD) basal media, without protein, protein hydrolysate and any animal-derived components, it suitable for high-density cell suspension expansion and transient transfection of different subtypes HEK293 cell lines (HEK293F, HEK293T, HEK293H, Expi293 and ect.), it can effectively support high-level expression of recombinant proteins, lentivirus and adenovirus, it can also be used in the development and production process of adenovirus related products.HEK293 CDM26 Pro combine with commercial feed media, can support high-density cell expansion, viability maintenance, and achieve efficient expression of target products.

 

Dry Powder/Liquid Medium 

Tobitec™ HEK293 CDM26 Pro medium can provide various specifications of culture medium Dry Powder-Bag, Liquid-Bottle, with the same performance and formula as liquid and dry powder medium. Tobitec™ HEK293 CDM26 Pro dry powder and liquid medium is produced without animal origin, protein.Tobitec™ HEK293 CDM26 Pro culture medium has the same performance and chemical defined.

 

Product Information

Animal origin free, protein-free, fully chemically defined culture media products;

Suitable for high density suspension culture of all derivatives of HEK293, with strong adaptability and rich nutrients;

Suitable for bioreactor large-scale scale-up culture processes, supporting batch, fed-batch and perfusion culture modes;

Effectively support transfection and subsequent product expression to ensure stable and high-quality expression of virus titers;

Highly quality imported raw materials to formulate the product with high quality and stability;

cGMP standard production conditions, using continuous needle milling equipment for power medium production to ensure good product consistency of different batches.

 

HEK293 Series Medium

The HEK293 media series includes HEK293 CDM26, HEK293 CDM26 Pro, HEK293 CDM15, HEK293 CDM15 Pro, HEK293 CDM30 and HEK293 CDM30 Pro, all of which are chemical defined media, animal origin-free medium specially designed for HEK293, HEK293F, HEK293T, HEK293H, Expi293 cell line . They can be used for the growth of HEK293 suspension cells high-density culture, adenovirus, AAV expression, and also lentivirus, proteins and other related products development and production process, can support high density cell expansion and stable product expression, suitable for large-scale manufacturing applications. Using appropriate feeding strategy based on cell strain traits can significantly improve cell growth and expression level and quality of antibody.


Specification

  • Cell type
    HEK293
  • Product type
    Chemically-defined
  • Culture type
    Suspension Cell Culture
  • Packing form
    LQ--Bottle;DP--Bag or Barrel
  • Form
    Liquid(LQ);Dry Powder(DP)
  • Specification
    LQ:500mL/1000mL;DP:10L/50L/100L

Storage condition

  • 2-8°C,Protect from light

Application case

Files and downloads

Find a Coa

  • Product information
    User's Manual—HEK293 CDM26 Pro (26-2)
    MSDS--HEK293 CDM26 Pro (26-2)
    PRODUCT SPECIFICATIONS--HEK293 CDM26 Pro (26-2)
    Declaration of Media Composition--HEK293 CDM26 Pro (26-2)
  • Product manual
    HEK293 Series Medium Products

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Frequently Asked Questions

  • Q1:What is the product qualification of the current culture medium? Does it comply with the listing declaration? Can you provide all the required materials?

    Resolve+

    A1:At present, media products are managed as first-class medical devices in China. Our production and quality of products comply with ISO13485 and cGMP standards. Currently, I am doing the filing of a class of medical devices, such as FDA MDF, which can support the marketing application and provide document support as required.
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