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View ProductsSize | 100ug, 1MG |
---|---|
Brand | ProteoGenix |
Product type | Recombinant Proteins |
Clonality | Monoclonal Antibody |
Expression system | XtenCHO |
Product name | Camalprin Biosimilar - Anti-AAT protein - Research Grade |
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Source | CAS: 2853491-11-7 |
Origin species | Human |
Expression system | XtenCHO |
Purity | >95% by SDS-PAGE |
Buffer | 0.01M PBS, pH 7.4 |
Delivery condition | Blue ice (+4°C) |
Delivery lead time in business days | 3-5 days if in stock; 3-5 weeks if production needed |
Storage condition | 4°C for short term; -20°C for long term |
Brand | ProteoGenix |
Aliases /Synonyms | anti-AAT, SPAAT, PI, Alpha-1 protease inhibitor, Alpha-1-antitrypsin, Alpha-1-antiproteinase, SERPINA1, Serpin A1 |
Reference | PX-TA2224-100 |
Note | For research use only. Not suitable for human use. |
Isotype | Human alpha-1-antitrypsin-variant |
Camalprin Biosimilar is a therapeutic protein that targets the Alpha-1 Antitrypsin (AAT) protein. It is a research grade product that has been developed as a biosimilar to the existing Camalprin medication. In this article, we will discuss the structure, activity, and potential applications of Camalprin Biosimilar in the field of therapeutic protein research.
Camalprin Biosimilar is a recombinant protein that is produced using advanced biotechnology techniques. It is a glycoprotein with a molecular weight of approximately 52 kDa. The protein is composed of 394 amino acids and has a complex three-dimensional structure that is essential for its activity.
The primary structure of Camalprin Biosimilar is similar to that of the native AAT protein, with minor differences in the amino acid sequence. However, the secondary and tertiary structures of Camalprin Biosimilar are different from the native AAT protein due to the use of different expression systems and post-translational modifications.
Camalprin Biosimilar is a potent inhibitor of neutrophil elastase, a protease enzyme that is responsible for breaking down proteins in the lungs. It works by binding to and inactivating neutrophil elastase, thereby preventing damage to the lung tissue. This activity is crucial in individuals with Alpha-1 Antitrypsin Deficiency, a genetic disorder that leads to low levels of AAT protein and increased risk of lung diseases such as emphysema and chronic obstructive pulmonary disease (COPD).
In addition to its role in AAT deficiency, Camalprin Biosimilar has also shown promising results in other conditions such as cystic fibrosis, bronchiectasis, and non-cystic fibrosis bronchiolitis. These conditions are characterized by increased levels of neutrophil elastase activity, and Camalprin Biosimilar can help in reducing the damage caused by this enzyme.
Camalprin Biosimilar has a wide range of potential applications in the field of therapeutic protein research. It can be used as a research tool to study the role of AAT protein in various diseases and to develop new treatments for conditions related to AAT deficiency.
Furthermore, Camalprin Biosimilar can also be used in clinical trials to evaluate its efficacy and safety in treating lung diseases. As a biosimilar, it has a similar mechanism of action and activity to the existing Camalprin medication, making it a promising alternative for patients who do not respond well to the current treatment or for those who cannot afford the high cost of the original medication.
Moreover, the production of Camalprin Biosimilar using recombinant technology allows for a consistent and reliable supply of the protein, making it more accessible for research and clinical use.
In conclusion, Camalprin Biosimilar is a research grade therapeutic protein that targets the AAT protein. It has a similar structure and activity to the existing Camalprin medication and has shown promising results in various lung diseases. Its potential applications in research and clinical settings make it a valuable tool in the field of therapeutic protein research. Further studies and clinical trials are needed to fully understand the potential of Camalprin Biosimilar and its role in treating AAT deficiency and related conditions.
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