LMH Cell Medium
SF501 serum-free medium for LMH cells
SF501 is a serum-free medium developed by Shanghai BioEngine for the suspension culture of LMH cells, supporting high-density growth and efficient expression of avian adenovirus vaccines. It provides a stable and efficient production process and has been widely applied in large-scale vaccine production projects.Description
Performance
Features
Serum-free
Animal-derived component-free
Protein-free
Support the suspension adaption of LMH cells
Support the high cell-density culture of LMH cells
Support high-efficiency amplification of avian adenovirus
Advantages
The first medium in China for industrial application of avian adenovirus production based on serum-free suspension culture of LMH cells;
EU certified ISO13485:2016 QMS and MDSAP (FDA) , all data are traceable;
4 advanced CMPM (Cone Mixing Pin Milling) powder media production lines to meet different customer demand with high inter-batch consistency (CPK*>1.33).
Powder media capable of a single batch size of 100,000 L.
Optional powder media for use in large-scale manufacturing with easy preparation procedures;
Strictly selected the "2 domestic+1 imported" raw material supplier model to to ensure a stable and reliable supply chain.
*CPK: Process Capability Index. CPK>1.33 indicates good process control and small inter-batch difference of products.

Order Information
Basal Medium
|
Application |
Product Name |
Cat. No. |
Size |
Size |
Product Instruction (pdf) |
Inquiries /Sample application |
|
Support high productivity of avian adenovirus vaccinea |
SF501 LMH Serumfree Meldum A | EXP0105704 |
200 L |
Powder |
||
| EXP0105702 |
10 L |
Powder |
Performance
Vaccines
LMH adherent cells could be directly acclimated in SF501 medium without serum. Rapidly adapting to the suspension culture system.

After acclimation from adherent to suspension culture, LMH cells exhibit were individually dispersed and translucent in morphology with a uniform cell size.

Successfully acclimated LMH suspension cells were inoculated at 1×106 cells/ml in SF501, and LMH cell density reached 5-7×106 cells/ml within 72 hours, with high viability for long-term stable passages.

LMH cells were inoculated at 1×106 cells/ml in SF501 medium and reached a maximum density of 2×107 cells/ml with a plateau period of up to 4 days.

Using SF501 medium, LMH cells are capable of producing avian adenovirus (serotype 4) without serum. The highest titer obtained reaches 109.3 TCID50/ml, comparable to that of adherent serous culture (108.7-9.3 TCID50/ml). Suspension culture allows for a significant increase in production efficiency.

Documents
LMH Cell Medium
DownloadFAQ
Q1:Is DMEM a complete medium?
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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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