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| Size | 100µg, 1MG |
|---|---|
| Isotype | [VH-h-CH2-CH3]-dimer |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Rimteravimab Biosimilar - Anti-Spike RBD mAb - Research Grade |
|---|---|
| Source | CAS: 2540797-21-3 |
| Species | Chimeric |
| 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 | Rimteravimab,VHH-72-Fc, XVR011,Spike RBD,anti-Spike RBD |
| Reference | PX-TA1804 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | [VH-h-CH2-CH3]-dimer |
| Clonality | Monoclonal Antibody |
Rimteravimab Biosimilar is a novel monoclonal antibody (mAb) that specifically targets the spike protein receptor binding domain (RBD) of the SARS-CoV-2 virus. This biosimilar is a research grade version of the original Rimteravimab antibody, which has shown promising results in treating COVID-19 patients. In this article, we will discuss the structure, activity, and potential applications of Rimteravimab Biosimilar as a therapeutic agent against COVID-19.
Rimteravimab Biosimilar is a recombinant humanized IgG1 mAb that is produced using Chinese hamster ovary (CHO) cells. It has a molecular weight of approximately 150 kDa and consists of two heavy chains and two light chains. The heavy chains are composed of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH), while the light chains contain two constant domains (CL) and one variable domain (VL).
The variable domains of Rimteravimab Biosimilar are responsible for its specificity and binding to the spike RBD of the SARS-CoV-2 virus. This binding occurs through the formation of hydrogen bonds and electrostatic interactions between the RBD and the complementary determining regions (CDRs) of the antibody. This results in the neutralization of the virus and prevents it from infecting host cells.
Rimteravimab Biosimilar has been shown to have potent antiviral activity against SARS-CoV-2 in both in vitro and in vivo studies. In vitro studies have demonstrated that the antibody can effectively block the binding of the virus to its receptor, angiotensin-converting enzyme 2 (ACE2), on the surface of human cells. This prevents the virus from entering the cells and replicating, thereby reducing the viral load.
In addition, Rimteravimab Biosimilar has also been shown to have a synergistic effect when combined with other antiviral agents, such as remdesivir. This combination has been found to have a greater inhibitory effect on the virus and can potentially reduce the risk of developing drug resistance.
The primary application of Rimteravimab Biosimilar is as a therapeutic agent for the treatment of COVID-19. It has been granted emergency use authorization by the FDA for the treatment of mild to moderate COVID-19 in high-risk patients. The biosimilar is currently undergoing clinical trials to evaluate its safety and efficacy in treating severe cases of COVID-19.
In addition to its use as a treatment for COVID-19, Rimteravimab Biosimilar also has potential applications in the prevention of the disease. It can be used as a prophylactic agent in individuals who have been exposed to the virus or in high-risk populations, such as healthcare workers. This can help reduce the spread of the virus and protect vulnerable individuals from developing severe illness.
Rimteravimab Biosimilar is a promising therapeutic agent for the treatment and prevention of COVID-19. Its unique structure and potent antiviral activity make it a valuable addition to the current arsenal of drugs being used to combat the pandemic. Further research and clinical trials are needed to fully understand the potential of this biosimilar and its role in controlling the spread of the SARS-CoV-2 virus.
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