Zaltenibart Biosimilar – Anti-Mannose-binding lectin-associated serine protease 1 mAb – Research Grade

Reference:
Product nameZaltenibart Biosimilar - Anti-Mannose-binding lectin-associated serine protease 1 mAb - Research Grade
SourceCAS: 2527079-60-1
Origin speciesHuman
Expression systemXtenCHO
Purity>95% by SDS-PAGE
Buffer0.01M PBS, pH 7.4
Delivery conditionBlue ice (+4°C)
Delivery lead time in business days3-5 days if in stock; 3-5 weeks if production needed
Storage condition4°C for short term; -20°C for long term
BrandProteoGenix
Aliases /Synonymsanti-Mannose-binding lectin-associated serine protease 1, CRARF, PRSS5, CRARF1, Mannose-binding protein-associated serine protease, Ra-reactive factor serine protease p100, Complement factor MASP-3, RaRF, MASP1, Mannan-binding lectin serine protease 1, Serine protease 5, Complement-activating component of Ra-reactive factor, MASP-1
ReferencePX-TA2221-100
NoteFor research use only. Not suitable for human use.
IsotypeIgG4-kappa
ClonalityMonoclonal Antibody

Description of Zaltenibart Biosimilar - Anti-Mannose-binding lectin-associated serine protease 1 mAb - Research Grade

Introduction
Zaltenibart Biosimilar – Anti-Mannose-binding lectin-associated serine protease 1 mAb – Research Grade is a therapeutic antibody that has been developed to target the mannose-binding lectin-associated serine protease 1 (MASP-1) protein. This biosimilar is a promising new treatment option for various diseases and conditions, and its unique structure and mechanism of action make it a valuable addition to the field of therapeutic antibodies.

Structure
Zaltenibart Biosimilar is a monoclonal antibody (mAb) that is produced through recombinant DNA technology. It is a fully humanized antibody, meaning that it is derived from human genetic material and has a structure similar to naturally occurring antibodies in the body. This makes it less likely to cause an immune response or side effects in patients.

The mAb is composed of two heavy chains and two light chains, which are linked together by disulfide bonds. The heavy chains contain the antigen-binding region, while the light chains are responsible for the antibody’s effector functions. The unique structure of Zaltenibart Biosimilar allows it to specifically target and bind to the MASP-1 protein with high affinity.

Activity
The primary activity of Zaltenibart Biosimilar is to inhibit the activity of MASP-1. MASP-1 is a serine protease that plays a crucial role in the activation of the complement system, a part of the immune system responsible for fighting off infections and foreign invaders. However, excessive activation of the complement system can lead to tissue damage and inflammation, which is seen in various diseases and conditions.

By binding to and inhibiting MASP-1, Zaltenibart Biosimilar helps to regulate the complement system and prevent excessive activation. This not only reduces tissue damage and inflammation but also allows the immune system to function more efficiently in fighting off infections. Additionally, Zaltenibart Biosimilar has been shown to have anti-inflammatory effects, further contributing to its therapeutic activity.

Application
Zaltenibart Biosimilar has a wide range of potential applications due to its ability to target and inhibit MASP-1. It is currently being studied for its potential use in various diseases and conditions, including autoimmune disorders, inflammatory diseases, and infectious diseases.

One of the most promising applications of Zaltenibart Biosimilar is in the treatment of autoimmune disorders, such as rheumatoid arthritis and lupus. These diseases are characterized by an overactive immune system that attacks healthy tissues, leading to chronic inflammation and tissue damage. By inhibiting MASP-1, Zaltenibart Biosimilar can help to regulate the immune response and reduce inflammation, providing relief to patients with these conditions.

In addition, Zaltenibart Biosimilar has shown potential in treating inflammatory diseases, such as inflammatory bowel disease and psoriasis. These conditions are also characterized by chronic inflammation, and the ability of Zaltenibart Biosimilar to regulate the complement system can help to alleviate symptoms and improve patient outcomes.

Furthermore, Zaltenibart Biosimilar has shown promise in the treatment of infectious diseases, particularly those caused by bacteria that activate the complement system. By inhibiting MASP-1, Zaltenibart Biosimilar can prevent the excessive activation of the complement system, which can lead to tissue damage and worsen the infection. This makes it a potentially valuable treatment option for conditions such as sepsis and pneumonia.

Conclusion
In conclusion, Zaltenibart Biosimilar – Anti-Mannose-binding lectin-associated serine protease 1 mAb – Research Grade is a promising therapeutic antibody with a unique structure and mechanism of action. By targeting and inhibiting MASP-1, it has the potential to treat a wide range of diseases and conditions, making it a valuable addition to the field of therapeutic antibodies. Further research and clinical trials are needed to fully understand the potential of Zaltenibart Biosimilar and its role in improving patient outcomes.

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