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| Size | 100µg, 1MG |
|---|---|
| Isotype | IgG1-kappa(Slience) |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Hu23B12 Biosimilar - Anti-TSLP mAb - Research Grade |
|---|---|
| Source | hu23B12 |
| Species | Homo sapiens |
| Expression system | XtenCHO |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3 week if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | anti-TSLP,Thymic stromal lymphopoietin,hu23B12 |
| Reference | PX-TA1902 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa(Slience) |
| Clonality | Monoclonal Antibody |
Hu23B12 Biosimilar is a research grade antibody that targets thymic stromal lymphopoietin (TSLP). This antibody is a biosimilar of the original Hu23B12 antibody, which was developed by Genentech Inc. for the treatment of allergic diseases. The biosimilar version is produced by a different company, but has been shown to have similar structure, activity, and application as the original antibody.
Hu23B12 Biosimilar is a monoclonal antibody (mAb) that is produced by recombinant DNA technology. 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 antigen-binding fragments (Fab) at the tips of the Y and a crystallizable fragment (Fc) at the base. The Fab regions are responsible for binding to the target molecule, TSLP, while the Fc region is involved in immune effector functions.
Hu23B12 Biosimilar specifically targets TSLP, a cytokine that plays a critical role in the development and progression of allergic diseases. TSLP is produced by epithelial cells in response to various stimuli, such as allergens, viruses, and bacteria. It then binds to its receptor on immune cells, including dendritic cells, T cells, and B cells, and triggers a cascade of events that lead to inflammation and allergic reactions.
By binding to TSLP, Hu23B12 Biosimilar blocks its interaction with its receptor, thereby inhibiting the downstream signaling pathways and reducing the production of pro-inflammatory cytokines. This results in a decrease in allergic responses, such as airway inflammation, mucus production, and bronchoconstriction. Additionally, the Fc region of the antibody can also activate immune cells, such as natural killer cells and macrophages, to further enhance the anti-inflammatory effects.
Hu23B12 Biosimilar has potential applications in the treatment of various allergic diseases, including asthma, atopic dermatitis, and allergic rhinitis. In preclinical studies, the original Hu23B12 antibody has shown promising results in reducing airway inflammation and improving lung function in animal models of asthma. It has also been shown to be effective in reducing skin inflammation and improving skin barrier function in models of atopic dermatitis.
Based on these preclinical data, clinical trials are currently underway to evaluate the safety and efficacy of Hu23B12 Biosimilar in human patients. If successful, this biosimilar could provide a more affordable treatment option for patients with allergic diseases, as well as increase the accessibility of this therapy to a larger population.
In summary, Hu23B12 Biosimilar is a research grade antibody that targets TSLP, a key cytokine involved in the development and progression of allergic diseases. This biosimilar has a similar structure, activity, and application as the original antibody, and has the potential to provide a more affordable treatment option for patients with allergic diseases. Further research and clinical trials are needed to fully evaluate the efficacy and safety of this biosimilar, but it holds great promise in the field of allergy treatment.
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