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| Size | 100µg, 1MG |
|---|---|
| Isotype | (scFv-heavy-kappa)-(scFv-heavy-lambda)-scFc |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Etevritamab Biosimilar - Anti-EGFR;CD3E mAb - Research Grade |
|---|---|
| Species | Bispecific scFv |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery lead time in business days | 3-5 days if in stock; 3-5 weeks if production needed |
| Delivery Time | 3-5 days if in stock; 3 week if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Etevritamab,,EGFR;CD3E,anti-EGFR;CD3E |
| Reference | PX-TA1837 |
| Note | For research use only. Not suitable for human use. |
| Isotype | (scFv-heavy-kappa)-(scFv-heavy-lambda)-scFc |
| Clonality | Monoclonal Antibody |
Etevritamab Biosimilar, also known as Anti-EGFR,CD3E mAb, is a research grade antibody that has shown promising results in the treatment of various cancers. This biosimilar is a monoclonal antibody that targets the epidermal growth factor receptor (EGFR) and CD3E, making it a potential therapeutic option for patients with EGFR-positive cancers.
Etevritamab Biosimilar is a chimeric monoclonal antibody, meaning it is composed of both human and mouse components. It is made up of two parts – the constant region and the variable region. The constant region is responsible for the antibody’s effector functions, while the variable region is responsible for binding to the target antigen.
The constant region of Etevritamab Biosimilar is derived from human IgG1, which allows for efficient binding to the Fc receptor on immune cells and activation of the immune response. The variable region is derived from a mouse antibody and has been engineered to have a high affinity for both EGFR and CD3E antigens.
Etevritamab Biosimilar works by binding to both EGFR and CD3E on the surface of cancer cells. EGFR is a receptor that is overexpressed in many types of cancer, and its activation leads to uncontrolled cell growth and survival. By binding to EGFR, Etevritamab Biosimilar blocks its activity and prevents the cancer cells from growing and spreading.
Additionally, Etevritamab Biosimilar also binds to CD3E, a protein found on the surface of T cells. This binding activates the T cells and triggers an immune response against the cancer cells. This dual mechanism of action makes Etevritamab Biosimilar a potent and targeted therapy for EGFR-positive cancers.
Etevritamab Biosimilar has shown promising results in preclinical studies and is currently being evaluated in clinical trials for the treatment of various cancers, including non-small cell lung cancer, head and neck cancer, and colorectal cancer.
cancer, Etevritamab Biosimilar has shown significant tumor shrinkage and improved survival rates in patients with EGFR-positive tumors. In head and neck cancer, Etevritamab Biosimilar has demonstrated a high response rate and prolonged progression-free survival. In colorectal cancer, Etevritamab Biosimilar has shown promising results in combination with other targeted therapies.
Etevritamab Biosimilar is currently in the research grade stage, which means it is still undergoing clinical trials and has not yet been approved for commercial use. However, the results from preclinical and early clinical studies are promising, and if approved, it has the potential to become an important treatment option for patients with EGFR-positive cancers.
In conclusion, Etevritamab Biosimilar is a chimeric monoclonal antibody that targets both EGFR and CD3E, making it a potential therapeutic option for patients with EGFR-positive cancers. Its unique mechanism of action and promising results in preclinical and clinical studies make it a promising candidate for cancer treatment. As research on Etevritamab Biosimilar continues, it has the potential to improve the outcomes and quality of life for patients with EGFR-positive cancers.
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