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| Size | 100ug, 1MG |
|---|---|
| Brand | ProteoGenix |
| Product type | Recombinant Proteins |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Trebananib Biosimilar - Anti-ANG-2 fusion protein - 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-ANG-2, ANGPT2, Angiopoietin-2 |
| Reference | PX-TA2036 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | Fusion - [IGHG1 Fc (Fragment constant) - [peptide 14-mer - peptide 14-mer]2] |
Trebananib Biosimilar, also known as Anti-ANG-2 fusion protein, is a research grade antibody that has shown promising results in the treatment of various diseases. This fusion protein has been designed to target and inhibit the activity of angiopoietin-2 (ANG-2), a protein that plays a crucial role in promoting blood vessel growth. In this article, we will explore the structure, activity, and potential applications of Trebananib Biosimilar in the field of biomedicine.
Trebananib Biosimilar is a fusion protein that is composed of two different components – a humanized monoclonal antibody and the extracellular domain of the ANG-2 receptor. The monoclonal antibody is designed to specifically bind to ANG-2, while the receptor domain acts as a decoy to neutralize the activity of ANG-2. This structure allows Trebananib Biosimilar to effectively block the interaction between ANG-2 and its receptor, thereby inhibiting the pro-angiogenic effects of ANG-2.
Trebananib Biosimilar works by targeting and inhibiting the activity of ANG-2, a protein that is involved in the regulation of blood vessel growth. ANG-2 is known to promote the formation of new blood vessels, a process called angiogenesis, which is essential for tissue growth and repair. However, in certain diseases such as cancer, ANG-2 can become overactive and promote abnormal blood vessel growth, leading to tumor growth and metastasis.
By binding to ANG-2 and blocking its interaction with its receptor, Trebananib Biosimilar effectively inhibits angiogenesis and prevents the formation of new blood vessels. This not only limits the supply of nutrients and oxygen to the tumor, but also disrupts its ability to spread to other parts of the body. In addition, Trebananib Biosimilar has been shown to enhance the activity of certain chemotherapeutic agents, making it a potential combination therapy for cancer treatment.
Trebananib Biosimilar has shown promising results in preclinical and clinical studies for the treatment of various diseases, particularly cancer. In a phase III clinical trial, Trebananib Biosimilar was evaluated as a treatment for ovarian cancer and showed significant improvement in progression-free survival when used in combination with chemotherapy. This suggests that Trebananib Biosimilar has the potential to be a valuable addition to the current treatment options for ovarian cancer.
In addition to cancer, Trebananib Biosimilar has also shown potential in the treatment of other diseases such as diabetic retinopathy and age-related macular degeneration. These diseases are characterized by abnormal blood vessel growth in the eye, which can lead to vision loss. By inhibiting angiogenesis, Trebananib Biosimilar has the potential to prevent or slow down the progression of these diseases.
Trebananib Biosimilar, also known as Anti-ANG-2 fusion protein, is a research grade antibody that has shown promising results in the treatment of various diseases. Its unique structure allows it to effectively target and inhibit the activity of ANG-2, a protein involved in promoting blood vessel growth. With its potential applications in cancer and other diseases, Trebananib Biosimilar holds great promise as a therapeutic agent in the field of biomedicine. Further research and clinical trials are needed to fully explore its potential and bring this promising treatment to patients in need.
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