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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG4, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Lipustobart Biosimilar - Anti-PD1 mAb - Research Grade |
|---|---|
| Species | Homo sapiens |
| Expression system | XtenCHO |
| Purity | >90% by SDS-PAGE. |
| Buffer | 0.01M PBS, pH 7.4. |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | 4°C for short term; -20°C for long term |
| Brand | ProteoGenix |
| Aliases /Synonyms | anti-PD1, Programmed cell death protein 1, Protein PD-1, hPD-1, PDCD1, CD279 |
| Reference | PX-TA2072 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Lipustobart Biosimilar – Anti-PD1 mAb – Research Grade: A Promising Antibody for
Lipustobart Biosimilar – Anti-PD1 mAb – Research Grade is a novel monoclonal antibody (mAb) that targets the programmed cell death protein 1 (PD-1) receptor. This biosimilar is designed to mimic the structure and function of the original anti-PD1 mAb, making it a potential therapeutic option for various types of cancer. In this article, we will delve into the structure, activity, and potential applications of this promising antibody in cancer immunotherapy.
Lipustobart Biosimilar – Anti-PD1 mAb is a fully humanized IgG4 antibody, meaning that it is derived from human genetic sequences and has minimal immunogenic potential. It is composed 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 Fab regions responsible for binding to the PD-1 receptor and one Fc region responsible for effector functions.
The Fab region of Lipustobart Biosimilar – Anti-PD1 mAb contains a complementarity-determining region (CDR) that specifically recognizes and binds to the PD-1 receptor on the surface of T cells. This binding inhibits the interaction between PD-1 and its ligands, PD-L1 and PD-L2, and prevents the suppression of T cell activity. The Fc region of the antibody also plays a crucial role in its activity by activating immune cells, such as natural killer (NK) cells and macrophages, to attack cancer cells.
The main activity of Lipustobart Biosimilar – Anti-PD1 mAb is its ability to block the PD-1/PD-L1 pathway, which is a major mechanism used by cancer cells to evade the immune system. By inhibiting this pathway, the antibody restores the function of T cells and enhances their ability to recognize and destroy cancer cells. Additionally, the antibody’s Fc region can trigger antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC), leading to the destruction of cancer cells.
Lipustobart Biosimilar – Anti-PD1 mAb has shown promising results in preclinical studies, demonstrating its ability to inhibit tumor growth and improve survival in animal models. In clinical trials, the antibody has also shown significant anti-tumor activity in patients with various types of cancer, including melanoma, non-small cell lung cancer, and renal cell carcinoma. It has been well-tolerated with manageable side effects, making it a promising candidate for cancer immunotherapy.
Lipustobart Biosimilar – Anti-PD1 mAb has the potential to be used as a monotherapy or in combination with other cancer treatments, such as chemotherapy, radiation therapy, and other immunotherapies. It has been granted orphan drug designation by the FDA for the treatment of certain types of cancer, highlighting its potential as a targeted therapy for rare and difficult-to-treat cancers.
Furthermore, Lipustobart Biosimilar – Anti-PD1 mAb has the potential to be used as a research tool for studying the PD-1/PD-L1 pathway and its role in cancer immunology. Its high specificity and potency make it a valuable tool for investigating the mechanisms of action of other anti-PD1 mAbs and developing new immunotherapies.
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