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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 | Minretumomab Biosimilar - Anti-TAG-72 mAb - Research Grade |
|---|---|
| Source | CAS 195189-17-4 |
| Species | Mus musculus |
| Expression system | Mammalian cells |
| 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 | Minretumomab,Mab CC-49,TAG-72,anti-TAG-72 |
| Reference | PX-TA1221 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-nd |
| Clonality | Monoclonal Antibody |
Minretumomab Biosimilar, also known as Anti-TAG-72 mAb, is a monoclonal antibody that has been developed as a biosimilar to the original Minretumomab antibody. It specifically targets the tumor-associated glycoprotein 72 (TAG-72), which is overexpressed in a variety of cancers. This article will provide a detailed description of the structure, activity, and potential applications of Minretumomab Biosimilar in the field of cancer therapy.
Minretumomab Biosimilar is a recombinant, humanized monoclonal antibody that is produced in a mammalian cell expression system. It consists of two identical heavy chains and two identical light chains, each with a molecular weight of approximately 150 kDa. The antibody has a Y-shaped structure, with two antigen-binding Fab regions at the tips of the Y and a constant Fc region at the base. The Fc region is responsible for mediating effector functions such as antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC).
Minretumomab Biosimilar specifically binds to the TAG-72 antigen, which is a mucin-like glycoprotein that is expressed on the surface of many types of cancer cells. This antigen is highly expressed in a variety of solid tumors, including ovarian, breast, colorectal, and pancreatic cancers. The binding of Minretumomab Biosimilar to TAG-72 leads to the inhibition of tumor growth and the induction of apoptosis (programmed cell death) in cancer cells.
In addition to its direct anti-tumor activity, Minretumomab Biosimilar also has immunomodulatory effects. It has been shown to enhance the activity of natural killer (NK) cells and macrophages, which are important components of the immune system’s defense against cancer. This further contributes to the antibody’s anti- cancer effects.
Minretumomab Biosimilar has shown promising results in preclinical studies and is currently being evaluated in clinical trials for its potential as a therapeutic agent in the treatment of cancer. It has been granted orphan drug designation by the US Food and Drug Administration (FDA) for the treatment of ovarian cancer, and is also being investigated for its efficacy in other types of cancer.
One potential application of Minretumomab Biosimilar is in combination with other anti- cancer therapies. Studies have shown that the antibody can enhance the effectiveness of chemotherapy and radiation therapy, making it a promising candidate for combination therapy in the treatment of cancer.
Another potential application of Minretumomab Biosimilar is in the field of targeted therapy. The specificity of this antibody for the TAG-72 antigen makes it a potential candidate for targeted delivery of drugs or imaging agents to cancer cells. This could potentially reduce the side effects of traditional chemotherapy and improve the efficacy of treatment.
In conclusion, Minretumomab Biosimilar is a promising antibody with potential applications in the field of cancer therapy. Its specific targeting of the TAG-72 antigen and its immunomodulatory effects make it a valuable addition to the arsenal of anti- cancer treatments. Further research and clinical trials are needed to fully understand the potential of this biosimilar in the treatment of cancer.
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