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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG1, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Prafnosbart Biosimilar - Anti-SKR1 mAb - 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-SKR1, Activin receptor type-1, Activin receptor-like kinase 2, TSR-I, ACVRLK2, ACTR-I, ALK-2, Serine/threonine-protein kinase receptor R1, TGF-B superfamily receptor type I, ACVR1, Activin receptor type I |
| Reference | PX-TA2084 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa |
| Clonality | Monoclonal Antibody |
Prafnosbart Biosimilar – Anti-SKR1 mAb – Research Grade is a monoclonal antibody (mAb) that specifically targets the SKR1 protein. This biosimilar has been developed as a potential therapeutic agent for the treatment of various diseases that are associated with SKR1 dysregulation. In this article, we will discuss the structure, activity, and potential applications of Prafnosbart Biosimilar in detail.
Prafnosbart Biosimilar is a recombinant humanized mAb that has been engineered to target the SKR1 protein. It is composed of two heavy chains and two light chains, which are connected by disulfide bonds. The heavy chains consist of a constant region and a variable region, while the light chains only have a variable region. The variable regions of both the heavy and light chains are responsible for binding to the SKR1 protein.
Prafnosbart Biosimilar binds specifically to the SKR1 protein with high affinity. This binding leads to the inhibition of SKR1 activity, which plays a crucial role in various signaling pathways involved in cell growth and survival. By inhibiting SKR1, Prafnosbart Biosimilar can potentially regulate cell proliferation and promote cell death in cancer cells.
In addition to its direct activity on SKR1, Prafnosbart Biosimilar also has an indirect effect on the immune system. It can bind to the Fc receptors on immune cells, such as natural killer cells and macrophages, and activate them to target and destroy cancer cells. This mechanism is known as antibody-dependent cell-mediated cytotoxicity (ADCC).
Prafnosbart Biosimilar has shown promising results in preclinical studies as a potential therapeutic agent for various cancers, including breast, lung, and prostate cancer. SKR1 is overexpressed in these cancers, making it an attractive therapeutic target. By inhibiting SKR1, Prafnosbart Biosimilar can potentially slow down tumor growth and induce cancer cell death.
In addition to cancer, SKR1 dysregulation has been implicated in other diseases, such as autoimmune disorders and neurodegenerative diseases. Prafnosbart Biosimilar may also have potential applications in these conditions, although further research is needed.
Prafnosbart Biosimilar is currently available in a research grade, which is suitable for in vitro and in vivo studies. This grade of the biosimilar is highly pure and has low endotoxin levels, making it suitable for sensitive experiments. Researchers can use Prafnosbart Biosimilar to study the role of SKR1 in various diseases and evaluate its potential as a therapeutic agent.
In summary, Prafnosbart Biosimilar – Anti-SKR1 mAb – Research Grade is a recombinant humanized mAb that specifically targets the SKR1 protein. It has shown promising results in preclinical studies as a potential therapeutic agent for various cancers and other diseases. Its unique structure and high binding affinity make it a promising candidate for further research and development. With the availability of a research grade, scientists can now study the potential of Prafnosbart Biosimilar in various disease models and pave the way for its future clinical use.
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