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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG4, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Zampilimab Biosimilar - Anti-TGM2 mAb - Research Grade |
|---|---|
| Source | CAS 2098280-42-1 |
| Species | Chimeric,Humanized |
| Purity | >85% |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Zampilimab,UCB-7858, UCB7858,TGM2,anti-TGM2 |
| Reference | PX-TA1541 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Zampilimab Biosimilar, also known as Anti-TGM2 mAb, is a monoclonal antibody that specifically targets and inhibits the activity of transglutaminase 2 (TGM2). TGM2 is an enzyme that plays a crucial role in various biological processes, including cell adhesion, apoptosis, and inflammation. Dysregulation of TGM2 has been linked to several diseases, making it an attractive therapeutic target. This article will provide a comprehensive overview of the structure, activity, and potential applications of Zampilimab Biosimilar in research.
Zampilimab Biosimilar is a fully humanized monoclonal antibody, meaning it is derived from human cells and has a high affinity for its target, TGM2. It is composed of two heavy chains and two light chains, each with a unique amino acid sequence. The heavy chains are further divided into variable (VH) and constant (CH) regions, while the light chains consist of variable (VL) and constant (CL) regions. The VH and VL regions come together to form the antigen-binding site, also known as the Fab region, which specifically recognizes and binds to TGM2.
Zampilimab Biosimilar works by binding to TGM2 and inhibiting its activity. TGM2 is a calcium-dependent enzyme that catalyzes the cross-linking of proteins, leading to the formation of insoluble protein aggregates. This process plays a crucial role in various physiological processes, but dysregulated TGM2 activity has been linked to the development of several diseases, including celiac disease, fibrosis, and cancer. By targeting and inhibiting TGM2, Zampilimab Biosimilar has the potential to modulate these disease processes and provide therapeutic benefits.
Due to its ability to specifically target and inhibit TGM2, Zampilimab Biosimilar has a wide range of potential applications in research. One of the primary uses of this antibody is in the study of celiac disease, an autoimmune disorder characterized by an immune response to gluten. TGM2 has been identified as a key player in the pathogenesis of celiac disease, and Zampilimab Biosimilar has shown promising results in preclinical studies as a potential treatment for this condition.
Another potential application of Zampilimab Biosimilar is in the treatment of fibrosis. Fibrosis is a process of excessive scarring that occurs in response to tissue injury and can result in organ dysfunction. TGM2 has been implicated in the development of fibrosis, and Zampilimab Biosimilar has shown promising results in preclinical studies as a potential therapy for fibrotic diseases.
In addition to celiac disease and fibrosis, Zampilimab Biosimilar may also have applications in the treatment of cancer. TGM2 has been shown to play a role in tumor growth and metastasis, and Zampilimab Biosimilar has shown potential in inhibiting these processes in preclinical studies. Further research is needed to fully explore the potential of Zampilimab Biosimilar in cancer treatment.
In conclusion, Zampilimab Biosimilar – Anti-TGM2 mAb is a promising therapeutic agent with a unique mechanism of action. Its ability to specifically target and inhibit TGM2 makes it a potential treatment for a variety of diseases, including celiac disease, fibrosis, and cancer. Further research and clinical trials are needed to fully evaluate the efficacy and safety of this antibody, but it holds great potential as a therapeutic option in the future.
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