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Animal Induced Pluripotent Stem Cell Culture Development
Induced pluripotent stem cells (iPSCs) are generated by the ectopic expression of one or more genes to reprogram adult cells. They are capable of unlimited self-renewal and can differentiate into almost any cell type when given a suitable microenvironment. In a large number of studies related to iPSCs, the in vitro culture of iPSCs is the foundation and basic technology for all research. BioVenic conducts in-depth research on the composition of culture media, growth factors and extracellular matrix to provide customers with advanced and reliable solutions for the development of cell culture systems. We support researchers worldwide by providing qualified, high-quality culture systems to generate and expand iPSCs in vitro, maintain cell viability, and determine differentiated cell types.
Background
Since its discovery, induced pluripotent stem cell technology has become a research hotspot in the fields of animal tissue engineering and veterinary regenerative medicine. The importance of their environmental conditions for in vitro survival has also received widespread attention. Excellent culture conditions not only support the intact maintenance of its totipotent form, but also facilitate its directed differentiation into the required adult cells. At the same time, iPSCs require stringent culture media and passage methods to maintain a healthy and undifferentiated state. This requires their maintenance by a culture system when cultured in vitro. BioVenic develops cell culture systems to regulate key cell life activities such as reprogramming, protection and differentiation, ensuring their effective use in animal disease research, veterinary drug discovery and normal animal development research.
Media Formulation Development
BioVenic develops dedicated high-quality culture media for each step of the entire in vitro application process of iPSCs. For integrative reprogramming or non-integrative reprogramming, basic in vitro proliferation and differentiation into various adult cells, our animal cell culture media design and development technology laboratory provides professional advice and reliable solutions according to customer needs. We select exclusive culture systems and solutions for customers to achieve target iPSC applications, scalability, and performance stability.
iPSC Maintenance and Culture
BioVenic offers a range of maintenance systems designed to support iPSCs in maintaining pluripotency throughout the expansion process and prior to differentiation. We have extensive expertise in developing and manufacturing advanced feeder-dependent and feeder-free culture systems to support our customers' individual research goals. We have designed fully integrated culture processes to maintain pluripotency in vitro, ensuring strict quality control at every stage.
Culture System | Features |
Feeder-dependent |
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Feeder-free |
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Culture Condition Optimization
BioVenic offers customized services for customer groups seeking to improve the performance of their existing iPSC culture media or culture systems. We have expertise in developing reliable pluripotent stem cell culture media that support pluripotency. We also have extensive project experience in improving and optimizing culture protocols. We select growth factors that maintain pluripotency from various expression systems based on the customer's ultimate goal. Our service also includes the selection of serum substitutes to increase biological activity and stability during cell growth and to ensure consistency in downstream experiments.
Cell Contamination Control
BioVenic effectively addresses common contamination issues encountered during in vitro cell culture in animal cell laboratories, particularly with the more delicate animal iPSCs. Across all cell culture related services, we help our clients overcome and prevent the negative consequences associated with contamination. These consequences include changes in cell status, reduced reproducibility of experimental results, and potential cell death. We closely monitor contamination and maintain strict quality control of animal cells and related products. Contamination of the culture system affects the survival and pluripotency of iPSC cultures, and mycoplasma negatively affects differentiation experiments, resulting in the waste of valuable reagents and samples. We use the contamination control platform to identify and improve bacteria, fungi, and mycoplasma in the culture system to create an in vitro culture environment for iPSCs with consistent pH, osmotic pressure, and absence of endotoxins.
Cell Contamination | Mycoplasma Contamination |
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Bacterial Contamination |
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Fungal Contamination |
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Animal iPSC Culture Tips
- Select high quality growing equipment and ingredients.
- Inspect and clean equipment regularly
- Optimize media formulation
- Improve operating procedures
- Monitor cell density regularly
- Verify pluripotency before differentiation
Why Choose Us?
Professional technical support and one-stop solutions for animal pluripotent stem cell culture.
Standardized culture system development process and multiple quality checks.
State-of-the-art cell detection platform and extensive experience in animal cell product development.
BioVenic has been involved in research projects focused on the development of animal cell culture systems for many years. Our laboratory rigorously selects high quality culture equipment for iPSC culture to maintain a sterile environment, ensuring the preservation and stability of the biological activity of iPSCs. Our technicians' working techniques are stable and standardized, which significantly reduces the loss of iPSCs during the process. During the service process, we carefully regulate cell density to ensure adequate nutrition and prevent excessive accumulation of metabolic waste. At the same time, we assess pluripotency using technical methods such as immunology, flow cytometry, or qPCR analysis. If your project requires technical support in animal cell culture, please contact us, we look forward to discussing your research needs in iPSC culture development.