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| Size | 100ug, 1MG |
|---|---|
| Brand | ProteoGenix |
| Product type | Recombinant Proteins |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Eflimrufusp Alfa Biosimilar - Anti-VEGF fusion protein - Research Grade |
|---|---|
| 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-VEGF |
| Reference | PX-TA2013 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | Fusion - [FLT1 (fms-related tyrosine kinase 1, vascular endothelial growth factor receptor 1, VEGFR-1, VEGFR, FLT, FRT, vascular permeability factor receptor) domain 2 fragment (132-232) - KDR (kinase insert domain receptor, vascular endothelial growth factor receptor 2, VEGFR2, VEGF-R2, FLK1, CD309) domain 3 fragment (227-327) - FGFR1 (fibroblast growth factor receptor 1, FLT2, KAL2) domains 2 and 3 fragment (150-361)]2 - IGHG1 Fc (Fragment constant) |
Eflimrufusp Alfa Biosimilar, also known as Anti-VEGF fusion protein, is a novel therapeutic antibody that has been developed as a biosimilar to the original Eflimrufusp Alfa. This biosimilar has been designed to mimic the structure and function of the original antibody, providing a more affordable and accessible treatment option for patients.
Eflimrufusp Alfa Biosimilar is a fusion protein that is composed of two different components – an antibody and a therapeutic target. The antibody component is a monoclonal antibody that specifically targets and binds to vascular endothelial growth factor (VEGF), a protein that plays a crucial role in the formation of new blood vessels. The therapeutic target component is a modified version of the original Eflimrufusp Alfa, which has been genetically engineered to enhance its therapeutic properties.
The antibody component of Eflimrufusp Alfa Biosimilar is made up of two heavy chains and two light chains, which are connected by disulfide bonds. The heavy chains consist of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH), while the light chains consist of two constant domains (CL) and one variable domain (VL). The variable domains are responsible for the specificity of the antibody, as they contain the antigen-binding site that recognizes and binds to VEGF.
The therapeutic target component of Eflimrufusp Alfa Biosimilar is a fusion protein that consists of the extracellular domain of VEGF receptor 1 (VEGFR1) and the Fc region of human immunoglobulin G1 (IgG1). This fusion protein acts as a decoy receptor, binding to VEGF and preventing it from binding to its natural receptors on the surface of endothelial cells. This effectively blocks the signaling pathway that promotes the formation of new blood vessels, which is important in the treatment of diseases such as cancer and age-related macular degeneration.
Eflimrufusp Alfa Biosimilar works by inhibiting the activity of VEGF, which is a key factor in the development and progression of various diseases. VEGF is a potent stimulator of angiogenesis, the process by which new blood vessels are formed from existing ones. In diseases such as cancer, VEGF promotes the growth of new blood vessels that supply nutrients and oxygen to the tumor, allowing it to grow and spread. In age-related macular degeneration, VEGF causes abnormal blood vessel growth in the retina, leading to vision loss.
By binding to VEGF and preventing it from binding to its natural receptors, Eflimrufusp Alfa Biosimilar blocks the signaling pathway that promotes angiogenesis. This helps to inhibit the growth and spread of tumors in cancer patients, and also prevents the abnormal blood vessel growth in the retina of patients with age-related macular degeneration.
Eflimrufusp Alfa Biosimilar has been approved for the treatment of various diseases, including metastatic colorectal cancer, non-small cell lung cancer, and age-related macular degeneration. It is administered through intravenous infusion and is typically used in combination with other standard treatments for these diseases.
As a biosimilar, Eflimrufusp Alfa Biosimilar provides a more affordable and accessible treatment option for patients, as it is typically priced lower than the original Eflimrufusp Alfa. It also has the potential to increase patient access to this important therapeutic antibody, as it can be manufactured and distributed more widely.
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