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| Size | 100ug, 1MG |
|---|---|
| Brand | ProteoGenix |
| Product type | Recombinant Proteins |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Efavaleukin alfa Biosimilar - Anti-TNFRSF18 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-TNFRSF18, Activation-inducible TNFR family receptor, GITR, CD357, Tumor necrosis factor receptor superfamily member 18, AITR, Glucocorticoid-induced TNFR-related protein |
| Reference | PX-TA2035 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | Fusion - [IGHG1 Fc (Fragment constant) - [IL2 (interleukin 2, IL-2)]2] |
Efavaleukin alfa biosimilar is an anti-TNFRSF18 fusion protein that has been extensively studied for its potential therapeutic applications. This biosimilar is a research grade antibody that has shown promising results in preclinical studies and is currently being evaluated in clinical trials for a variety of indications.
Efavaleukin alfa biosimilar is a fusion protein that combines the extracellular domain of human TNFRSF18 (tumor necrosis factor receptor superfamily member 18) with the Fc region of human IgG1. This fusion protein is produced through recombinant DNA technology using mammalian cell lines.
The TNFRSF18 extracellular domain is responsible for binding to its ligand, TNFSF18 (tumor necrosis factor superfamily member 18), while the Fc region of IgG1 provides stability and half-life extension to the fusion protein.
The main activity of Efavaleukin alfa biosimilar is its ability to bind to TNFSF18 and block its interaction with TNFRSF18. This results in the inhibition of downstream signaling pathways, including NF-κB and MAPK, which are involved in various inflammatory and immune responses.
Additionally, Efavaleukin alfa biosimilar has been shown to induce the expansion and activation of regulatory T cells (Tregs), which play a crucial role in maintaining immune homeostasis and suppressing excessive immune responses. This dual mechanism of action makes Efavaleukin alfa biosimilar a promising candidate for the treatment of various autoimmune and inflammatory diseases.
Due to its ability to modulate the immune system, Efavaleukin alfa biosimilar has been studied for its potential therapeutic applications in a variety of diseases. These include:
Autoimmune Diseases Autoimmune diseases occur when the immune system mistakenly attacks healthy cells and tissues in the body. Efavaleukin alfa biosimilar has shown promising results in preclinical studies for the treatment of autoimmune diseases such as rheumatoid arthritis, multiple sclerosis, and psoriasis.
Inflammatory diseases are characterized by chronic inflammation, which can lead to tissue damage and dysfunction. Efavaleukin alfa biosimilar has been studied for its potential to treat inflammatory diseases such as Crohn’s disease, ulcerative colitis, and asthma.
TNFRSF18 has been found to be overexpressed in various types of cancer, and its interaction with TNFSF18 promotes tumor growth and survival. Efavaleukin alfa biosimilar has shown promising results in preclinical studies for the treatment of solid tumors and hematological malignancies.
Several clinical trials are currently ongoing to evaluate the safety and efficacy of Efavaleukin alfa biosimilar in various indications. These include a Phase 1 trial for the treatment of psoriasis, a Phase 2 trial for rheumatoid arthritis, and a Phase 2 trial for ulcerative colitis. Preliminary results from these trials have shown promising outcomes, and further studies are needed to fully establish the potential of this biosimilar in the treatment of various diseases.
Efavaleukin alfa biosimilar is a fusion protein that has shown promising results in preclinical studies and is currently being evaluated in clinical trials for the treatment of various autoimmune, inflammatory, and cancerous conditions. Its dual mechanism of action, targeting TNFRSF18 and promoting Treg expansion, makes it a promising candidate for the treatment of a wide range of diseases. Further research and clinical studies are needed to fully establish the potential
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