NK Cell Medium
HIPP series serum-free medium for lymphocytes
BioEngine developed a serum-free medium named HIPP-T009 in 2018 for the in vitro culture of lymphocytes, which is an excellent option for large-scale culture of T-cells, NK cells, CAR-T, CIK, CAR-NK, hematopoietic stem cells, and other cell lines like NK-92, NK-92MI, K562, Jurkat, etc. HIPP-T009 eliminates the need for serum or serum substitutes, ensuring high safety and stability during the culture process. In 2020, HIPP-T009 became the first Chinese cell culture medium used in cell therapy clinical trials in China, demonstrating its potential as a reliable and efficient cell culture medium for various applications.Description
Performance
Features
Xeno-free, contains no growth factors, synthetic activators, or undefined components
Universality and flexibility: Applicable for the culture of T-cell, NK cell, CAR-T, CIK, CAR-NK, hematopoietic stem cells and other types of cell lines (NK-92, NK-92MI, K562, Jurkat, etc.)
High performance in cell expansion and high-density culture under completely serum-free condition
Advantages
The 1st approved Chinese culture medium used in cell therapy clinical trials;
No need to add serum, plasma, or serum substitutes, hence it minimizes batch-to-batch variation in the culture process and simplifies the declaration process for IND/NDA applications;
Manufactured under the cGMP guidelines and ISO13485 quality system, meet regulatory requirements in different countries;
Innovative "2 domestic+1 imported" raw material supplier modal ensures a stable supply chain to face the fluctuations and uncertainty in the raw material market;
The comprehensive set of DMR documents for audit.

Order Information
Basal Medium
|
Application |
Product Name |
Cat. No. |
Size |
Form |
Product Instruction (pdf) |
Inquiries /Sample application |
| HIPP-X100 Kit | HIPP-X100 Lymphocyte Serum-free Medium (Without phenol red, GMP Grade) | EXP0122701 | 1 L | Liquid | ||
| HIPP-X100 Lymphocyte Serum-free Medium Supplement | EXP0122801 | 5ml | Liquid | |||
|
T-cell, NK cell, CAR-T, CIK, CAR-NK-92, hematopoietic stem cells and other types of cell lines (NK-92, NK-92MI, K562, Jurkat, etc.) |
HIPP-T009 Lymphocyte Serum-free Medium (Without phenolred, GMP Grade) |
EXP0103801 |
1 L |
Liquid |
||
| HIPP-T009 Lymphocyte Serum-free Medium (With phenol red, Research Grade) |
EXP0118701 |
1 L |
Liquid |
|||
| HIPP-T006 Lymphocyte Serum-free Medium (Without phenolred, GMP Grade) |
EXP0105301 | 1L |
Liquid |
|||
| HIPP-T006 Lymphocyte Serum-free Medium (With phenol red, Research Grade) |
EXP0118801 |
1L |
Liquid |
Performance
Cell and Gene Therapy
CIK cell culture
Without adding any serum, the expansion fold of CIK cells during 14 days of culture in a completely serum-free HIPP-T009 medium was significantly higher than that of global Brand A. Even compared with global Brand A with 5% serum added, CIK cell expansion fold and phenotype (CD3+CD56+) in completely serum-free HIPP-T009 are still higher (see below). HIPP-T009 effectively supports the high-efficiency expansion and directed differentiation of CIK cells.

NK cell culture (With Feeder)
Without adding any serum, the expansion performance of NK cells in the completely serum-free HIPP-T009 for 14 days was significantly higher than that of global Brand A. Even compared with global Brand A with 5% serum added, NK cell expansion fold and phenotype (CD3-CD56+) in completely serum-free HIPP-T009 are still higher (see below). HIPP-T009 effectively supports the high-efficiency expansion and directed differentiation of NK cells.

NK-92 cell culture
Under the same conditions, when cultured in completely serum-free HIPP-T009 for 36 days, the expansion fold and CD3-CD56+ phenotype of NK-92 cells were higher than those in α-MEM supplemented with 12.5% horse serum and 12.5% fetal bovine serum (see below).

Documents
T Cell Medium
DownloadFAQ
Q1: What is NK cell?
Q2:What does RPMI 1640 stand for?
Q3: What is the process of development and differentiation of NK cells?
Q4:What are the methods for suspension cells passaging?
Q5:How to prevent cell contamination and cross-contamination?
Q6:What are the different production platforms for COVID-19 vaccines?
Q7:How do I prepare cell culture media from powder?
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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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