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| Size | 100ug, 1MG |
|---|---|
| Isotype | F(ab')2-G1-nd |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Igovomab Biosimilar - Anti-MUC16 mAb - Research Grade |
|---|---|
| Source | CAS 171656-50-1 |
| Species | Mus musculus |
| 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 | Igovomab,Indimacis 125,OC125 chelator DTPA,MUC16,anti-MUC16 |
| Reference | PX-TA1084 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | F(ab')2-G1-nd |
| Clonality | Monoclonal Antibody |
Igovomab biosimilar, also known as Anti-MUC16 mAb, is a monoclonal antibody that has been developed as a potential therapeutic agent for the treatment of various cancers. This biosimilar is a research-grade version of the original Igovomab, which was first approved for clinical use in 1995. In this article, we will explore the structure, activity, and potential applications of this novel antibody.
Igovomab biosimilar is a recombinant humanized IgG1 monoclonal antibody that specifically targets the MUC16 antigen. The MUC16 antigen, also known as CA125, is a cell surface glycoprotein that is overexpressed in many types of cancers, including ovarian, breast, and lung cancer. The biosimilar is composed of two heavy chains and two light chains, each containing a variable region that binds to the MUC16 antigen and a constant region that mediates effector functions.
The primary mechanism of action of Igovomab biosimilar is its ability to bind to the MUC16 antigen on cancer cells. This binding triggers a series of downstream events that ultimately lead to the destruction of the cancer cells. The biosimilar can also recruit immune cells, such as natural killer cells and macrophages, to the site of the tumor through its Fc region, enhancing its anti- cancer activity.
In addition to its direct anti-tumor effects, Igovomab biosimilar has been shown to have immunomodulatory effects. It can induce the production of cytokines and chemokines, which are important signaling molecules involved in the immune response against cancer. This can further enhance the body’s natural defense mechanisms against cancer cells.
The primary application of Igovomab biosimilar is in the treatment of cancers that overexpress the MUC16 antigen. These include ovarian, breast, and lung cancer, as well as other types of solid tumors. The biosimilar can be used as a single agent or in combination with other anti- cancer therapies, such as chemotherapy or radiation therapy.
In addition to its potential as a therapeutic agent, Igovomab biosimilar also has potential applications in cancer diagnosis and monitoring. The MUC16 antigen is commonly used as a biomarker for many types of cancers, and the biosimilar can be used to detect and measure levels of this antigen in the blood. This can aid in the early detection of cancer and in monitoring the response to treatment.
While Igovomab biosimilar has shown promising results in preclinical and clinical studies, further research is needed to fully understand its potential. Ongoing studies are exploring the use of this biosimilar in combination with other therapies, as well as its potential in other types of cancers. Additionally, efforts are being made to improve the efficacy and safety of the biosimilar through modifications to its structure and formulation.
In summary, Igovomab biosimilar, also known as Anti-MUC16 mAb, is a promising therapeutic agent for the treatment of cancers that overexpress the MUC16 antigen. Its unique structure and activity make it a potential candidate for use as a single agent or in combination with other anti- cancer therapies. Ongoing research and development will continue to shed light on the potential applications of this biosimilar in the fight against cancer.
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