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| Size | 100µg, 1MG |
|---|---|
| Isotype | IgG1-kappa -[scFv]2 |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Ivonescimab Biosimilar - Anti-VEGF & PD1 mAb - Research Grade |
|---|---|
| Source | CAS: 2428381-53-5 |
| Species | Humanized |
| Expression system | XtenCHO |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3 week if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Ivonescimab,AK 112, AK-112, AK112,VEGF & PD1,anti-VEGF & PD1 |
| Reference | PX-TA1763 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa-[scFv]2 |
| Clonality | Monoclonal Antibody |
Ivonescimab Biosimilar is a novel, research-grade monoclonal antibody (mAb) designed to target two key therapeutic pathways: vascular endothelial growth factor (VEGF) and programmed death-1 (PD1). This promising therapeutic agent has the potential to revolutionize the treatment of various diseases, including cancer, by inhibiting the growth and spread of tumors. In this article, we will discuss the structure, activity, and application of Ivonescimab Biosimilar in detail.
Ivonescimab Biosimilar is a recombinant, humanized mAb that is produced using advanced biotechnology techniques. It is a fusion protein consisting of two distinct regions – the constant region (Fc) and the variable region (Fab). The Fc region of the antibody is responsible for binding to the Fc receptors on immune cells, while the Fab region binds specifically to its target molecules, VEGF and PD1.
The Fc region of Ivonescimab Biosimilar is derived from a human IgG1 antibody, which ensures its stability and prolonged half-life in the body. The Fab region is engineered to bind to both VEGF and PD1 with high specificity and affinity, making it a potent therapeutic agent.
The primary mode of action of Ivonescimab Biosimilar is through its dual targeting of VEGF and PD1. VEGF is a key growth factor that promotes the formation of new blood vessels, a process known as angiogenesis. In cancer, VEGF plays a crucial role in tumor growth and metastasis by supplying oxygen and nutrients to the tumor cells. By binding to VEGF, Ivonescimab Biosimilar inhibits angiogenesis and thus limits the growth and spread of tumors.
PD1 is a checkpoint protein that regulates the immune response by inhibiting the activity of T cells. In cancer, PD1 is overexpressed on tumor cells, allowing them to evade detection and destruction by the immune system. Ivonescimab Biosimilar blocks the interaction between PD1 and its ligands, PD-L1 and PD-L2, thereby activating T cells and enhancing the immune response against cancer cells.
In addition to its anti-VEGF and anti-PD1 activity, Ivonescimab Biosimilar also has a direct cytotoxic effect on cancer cells. It induces cell death by binding to specific receptors on the surface of cancer cells and triggering a series of signaling pathways that lead to cell death.
Ivonescimab Biosimilar has shown promising results in preclinical studies and is currently being evaluated in clinical trials for the treatment of various cancers, including lung, breast, and colorectal cancer. It has also shown potential in the treatment of other diseases, such as age-related macular degeneration and diabetic retinopathy, where VEGF plays a critical role.
The unique dual targeting of VEGF and PD1 by Ivonescimab Biosimilar makes it a versatile therapeutic agent with the potential to be used in combination with other treatments, such as chemotherapy and immunotherapy, to enhance their effectiveness.
In summary, Ivonescimab Biosimilar is a novel, research-grade monoclonal antibody that targets both VEGF and PD1. Its unique structure and mode of action make it a promising therapeutic agent for the treatment of various diseases, particularly cancer. As more research is conducted, Ivonescimab Biosimilar has the potential to become a game-changing treatment option for patients in need.
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