MDCK Cell Culture Medium
Xeno series serum-free medium for MDCK cells
BioEngine's R&D team commenced MDCK cell culture research in 1995 and has since developed the Xeno series and SF003 MDCK serum-free media using a high-throughput AI data screening platform. The Xeno series supports high-density cultures and efficient proliferation of various flu virus subtypes. The SF003 media is suitable for avian and swine influenza virus proliferation and has been used in industrial production projects.Description
Performance
Features
Serum-free
Animal-derived component-free
Protein-free
Support rapid serum-free suspension adaptation of adherent MDCK cells
Support high-efficiency proliferation and high-density culture of MDCK cells
Xeno supports high-efficiency proliferation of the human flu virus
SF003 supports high-efficiency proliferation of avian influenza and swine influenza viruses
Advantages
ADCF; TSE/BSE statement available on demand;
Distinctive culture results proven in numerous studies on human flu virus subtypes;
Optional powder media for use in large-scale manufacturing with easy preparation procedures;
Powder media capable of a single batch size of 100,000 L;
Full traceability by EU-certified ISO13485:2016 QMS and MDSAP (FDA);
Excellent inter-batch consistency (CPK* > 1.33);
Complete documents in support of CTA for easier regulatory submission.

Advantages
Distinctive culture results proven in numerous studies on avian influenza virus subtypes;
Optional powder media for use in large-scale manufacturing with easy preparation procedures;
Powder media capable of a single batch size of 100,000 L;
Excellent inter-batch consistency (CPK* > 1.33);
Full traceability by EU-certified ISO13485:2016 QMS and MDSAP (FDA);
*CPK is a standard index to state the capability of one process. CPK>1.33: the process is capable and meets specification limits. The higher the CPK, the better.

Order Information
Basal Medium
|
Application |
Product Name |
Cat. No. |
Size |
Form |
Product Instruction (pdf) |
Inquiries /Sample application |
|
MDCK cells Support high-efficiency proliferation of the human flu virus |
Xeno-S001S MDCK Serum-free Medium | EXP0100407 |
200 L |
Powder |
||
| EXP0100403 |
10 L |
Powder |
||||
| SF003 MDCK Serum-free Medium | EXP0116704 |
200 L |
Powder |
|||
| EXP0116703 |
10 L |
Powder |
Performance
Xeno
Cell Growth
MDCK adherent cells were directly acclimated to suspension culture using Xeno-S001S medium, enabling rapid adaption and stable growth with a doubling time of 10-24 hours. After acclimation, the suspended MDCK cells exhibit a well-rounded and uniform morphology, with individual dispersed and no cell clumping.

Xeno media could support a high cell density of up to 2.0 × 107 cells/ml for MDCK suspension cells, approximately twice compared to other serum-free media.

Virus Production
Using Xeno-S001S medium, different subtypes of influenza viruses can achieve an HA titer ranging from 29 to 212 HAU/25μl.

Using Xeno-S001S medium, different subtypes of influenza viruses can achieve titers ranging from 28 to 29 TCID50/ml.

SF003
Virus production
Using Xeno-S001S medium, different subtypes of influenza viruses can achieve an HA titer ranging from 29 to 212 HAU/25μl.

Using Xeno-S001S medium, different subtypes of influenza viruses can achieve titers ranging from 27 to 212 TCID50/ml.

Using Xeno-S001S medium, different subtypes of influenza viruses can achieve HI titers can reach 27 ~212 HIU/25μl.

Documents
SF003 MDCK Cell Culture Media
DownloadFAQ
Q1:What media is used for MDCK cells?
Q2:What is the function of the MDCK cell?
Q3:What is the MDCK cell line culture?
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Antibodies
In fed-batch process, CHO cells cultured in Eden CD CHO media demonstrate higher viable cell density (VCD) and protein production than competitors. On average, the antibody titers of various CHO cell lines cultured in Eden CD CHO media ranged from 2 to 11 g/L.

In the pulse perfusion process, CHO cells cultured in Eden CD CHO media demonstrated superior performance than competitive global brands. When VVD=1.0, volumetric productivity (Vp) can reach up to 2.2 g/L/day, and the cumulative product expression in 14 days can reach 19 g/L, 55% higher than global brand B. When VVD=2.0, Vp can reach up to 3.3g/L/day, and the cumulative product expression in 14 days can reach 25 g/L.

Brochures
| CHO Cell Medium |
FAQ
Q1: What is the packaging for BioEngine's powder media?
Q2: Can we seal the bag if there is leftover powdered medium?
Q3: What is the shelf life of BioEngine's Eden series CHO cell culture media, and how do you verify the expiration date?
Q4: Does BioEngine offer any regulators or additives for modulating antibody glycosylation?
Q5: Does BioEngine's CHO cell culture media contain hydrolysates, insulin, cytokines, or other components?
Q6: What are CHO media?
Q7: What are the differences between DMEM and RPMI?
1. Nutrient composition: DMEM (Dulbecco's Modified Eagle's Medium) and RPMI (Roswell Park Memorial Institute) have different nutrient compositions. DMEM contains higher levels of glucose, amino acids, vitamins, and sodium pyruvate, while RPMI has a lower glucose concentration and a different amino acid and vitamin composition.
2. pH: DMEM has a higher pH (7.4-7.6) compared to RPMI (7.2-7.4).
3. Usage: DMEM is a more general-purpose medium and can be used for a wide range of cell types, including adherent and non-adherent cells, while RPMI is typically used for the culture of immune cells such as lymphocytes and hybridomas.
4. Serum requirement: RPMI is often used with lower serum concentrations (e.g. 5-10%) than DMEM, which may require higher serum concentrations (e.g. 10-20%).
Overall, the choice between DMEM and RPMI depends on the specific cell type being cultured and the experimental conditions.
Q8: What is a fed-batch culture?
The goal of a fed-batch culture is to maximize cell growth and productivity while maintaining a stable culture environment. By controlling the rate and timing of nutrient addition, the culture can be kept in a state of controlled growth, avoiding the depletion of nutrients and accumulation of waste products that can limit growth and product formation in batch cultures. Additionally, the use of a fed-batch culture can allow for the accumulation of high cell densities and the optimization of production conditions, leading to higher yields and greater efficiency in bioprocesses.
Q9: What are the advantages of suspension cell cultures?
1. Scalability: Suspension cell cultures can be easily scaled up to produce large quantities of cells. This makes them particularly useful for biomanufacturing and the production of recombinant proteins.
2. Flexibility: Suspension cultures can be adapted to a wide range of culture conditions, such as pH, temperature, and nutrient availability. This allows for the optimization of cell growth and productivity.
3. Homogeneity: Suspension cultures provide a more homogeneous population of cells than adherent cultures, where cells may exhibit varying degrees of differentiation and proliferation.
4. Reduced risk of contamination: Suspension cultures are less prone to contamination by bacteria or fungi than adherent cultures, as there are no surfaces for microorganisms to adhere to.
5. Ease of harvesting: Cells in suspension culture can be easily harvested using centrifugation, filtration, or other methods. This simplifies downstream processing and reduces the risk of damage to the cells.
Overall, suspension cell culture offers several advantages over other types of cell culture, particularly in the context of large-scale biomanufacturing and the production of recombinant proteins.
Q10: What is gene therapy?
●Replacing a disease-causing gene with a healthy copy of the gene.
●Inactivating or deleting a disease-causing gene.
●Introducing a new or modified gene to help fight disease.
Gene therapy is a promising and innovative field of medicine that has potential applications for many diseases, such as cancer, genetic disorders, infectious diseases, and autoimmune diseases 23. However, gene therapy also faces many challenges and risks, such as safety, efficacy, ethical issues, and regulatory hurdles.
Gene therapy usually be delivered to the cells by virus vector, such as AAV, Adv and RV. BioEngine provides vigor series insect cell media for large scale AAV production."
Q11: Does BioEngine provides serum products, like FBS?
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