In process Protein Detection
Protein fermentation
Protein fermentation plays a crucial role in the pharmaceutical industry, enabling the production of a wide range of biopharmaceuticals, including therapeutic proteins and enzymes. This process involves the use of microorganisms such as bacteria, yeast, or mammalian cells to produce proteins in a controlled environment.
The fermentation process can be divided into two main stages: upstream and downstream processing. Upstream processing focuses on the growth and maintenance of the microbial culture, optimizing conditions such as temperature, pH, and nutrient supply to maximize protein production. Downstream processing involves the purification and refinement of the produced proteins, ensuring they meet the required quality standards for pharmaceutical use[1][2].
Protein fermentation is essential for producing complex biologics like monoclonal antibodies, insulin, and growth hormones, which are used to treat various medical conditions. This method offers scalability, cost-effectiveness, and the ability to produce high-quality proteins consistently[1][3].

However, to produce proteins in an efficient manner, it is important to monitor protein concentrations during the fermentation process. Determining protein concentration during the fermentation process presents several challenges with conventional methods:
Protein measurement during Fermentation

Technology

List of some functionalized μbeads for protein detection in Fermentation:
- Anti-His μBeads (His-tagged proteins)
- Anti-GST μBeads (GST-tagged proteins)
- Neutravidin/ Streptavidin μBeads (biotinylated Proteins)
- Biotin μBeads (Avidins, Avidin-bound proteins)
- Protein A/G μBeads (Antibodies)
- Anti-FLAG μBeads (Flagged proteins)
- Costumer specific binding molecule μBeads (untagged proteins)
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