Dulbecco's Medium
Dulbecco's Modified Eagle Medium (DMEM) is a widely used basal medium in cell culture, particularly for culturing mammalian cells. It was originally developed by Renato Dulbecco and colleagues as a modification of Eagle's Minimum Essential Medium (MEM) to support the growth of a wide range of cell types.
Key Components
- Amino Acids: DMEM contains a variety of essential amino acids, including L-glutamine, which is crucial for protein synthesis and cell growth.
- Vitamins: The medium is supplemented with vitamins such as pyridoxine (vitamin B6), riboflavin (vitamin B2), and others that are essential for cell metabolism.
- Glucose: DMEM is available in formulations with either low glucose (1 g/L) or high glucose (4.5 g/L) concentrations. The high glucose version is used for cells with higher energy demands.
- Salts: Sodium chloride, potassium chloride, calcium chloride, and magnesium sulfate provide the necessary ions to maintain osmotic balance and membrane potential.
- Buffer System: Sodium bicarbonate is included to maintain pH stability in a CO₂ incubator environment.
- Phenol Red: A pH indicator dye is added to monitor the pH of the medium.
Applications
- Cell Culture: DMEM is widely used for culturing fibroblasts, neurons, and various other primary and immortalized cell lines.
- Transfection Studies: It supports the growth conditions necessary for transfection experiments and other cell-based assays.
- Tissue Engineering: DMEM is also used as a basal medium in tissue engineering applications.
Variants
- Low Glucose DMEM: Typically used for cells with lower energy requirements.
- High Glucose DMEM: Used for cells with higher energy demands or in high-density cultures.
- DMEM/F-12: A 1:1 mixture of DMEM and Ham's F-12 medium, designed for more complex cell culture systems requiring additional nutrients.
In summary, DMEM is a versatile and essential medium in cell biology, providing the basic nutrients and environmental conditions necessary for the maintenance and growth of various cell types in vitro.
|
|
|
|
|
|
|