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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG1-nd |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Fontolizumab Biosimilar - Anti-IFNG mAb - Research Grade |
|---|---|
| Source | CAS 326859-36-3 |
| Species | Humanized |
| Expression system | Mammalian cells |
| Molecular weight | 150kDa |
| 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 | Fontolizumab,HuZAF,IFNG,anti-IFNG |
| Reference | PX-TA1043 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-nd |
| Clonality | Monoclonal Antibody |
Fontolizumab Biosimilar, also known as Anti-IFNG mAb, is a monoclonal antibody that targets the cytokine interferon-gamma (IFN-γ). This antibody has been developed as a potential therapeutic agent for various inflammatory and autoimmune diseases. In this article, we will discuss the structure, activity, and potential applications of Fontolizumab Biosimilar.
Fontolizumab Biosimilar is a chimeric monoclonal antibody, meaning it is composed of both human and non-human components. The antibody is composed of two identical heavy chains and two identical light chains, each with a molecular weight of approximately 25 kDa. The heavy and light chains are connected by disulfide bonds and form a Y-shaped structure.
The variable regions of the antibody, responsible for binding to IFN-γ, are derived from a mouse monoclonal antibody. The constant regions of the antibody, responsible for effector functions, are derived from a human antibody. This chimeric structure allows for specific binding to IFN-γ while also minimizing the potential for immune reactions.
Fontolizumab Biosimilar works by binding to IFN-γ and preventing it from binding to its receptor on target cells. This inhibits the downstream signaling pathways that lead to inflammation and autoimmune responses. Additionally, the binding of Fontolizumab Biosimilar to IFN-γ can also lead to the depletion of IFN-γ-producing cells, further reducing the levels of this cytokine in the body.
IFN-γ is a key player in the immune response, and its dysregulation has been linked to various diseases such as rheumatoid arthritis, Crohn’s disease, and psoriasis. By targeting IFN-γ, Fontolizumab Biosimilar has the potential to treat these diseases and provide relief to patients.
Fontolizumab Biosimilar is currently being studied as a potential treatment for various inflammatory and autoimmune diseases. Clinical trials have shown promising results in the treatment of rheumatoid arthritis, with improvements in symptoms and reduction in disease activity. Similarly, studies have also shown potential for Fontolizumab Biosimilar in the treatment of Crohn’s disease and psoriasis.
In addition to these conditions, Fontolizumab Biosimilar is also being investigated for its potential in treating other autoimmune diseases such as multiple sclerosis and lupus. The antibody’s ability to specifically target IFN-γ makes it a promising candidate for these diseases, which are characterized by dysregulated immune responses.
In summary, Fontolizumab Biosimilar is a chimeric monoclonal antibody that targets the cytokine IFN-γ. Its unique structure allows for specific binding to IFN-γ while minimizing the potential for immune reactions. This antibody has shown promising results in the treatment of various inflammatory and autoimmune diseases, making it a potential therapeutic option for patients in the future. Further research and clinical trials are needed to fully understand the potential of Fontolizumab Biosimilar and its role in the treatment of these diseases.
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