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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG1, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Ranevetmab Biosimilar - Anti-NGF, NGFB mAb - Research Grade |
|---|---|
| Source | CAS 1632282-27-9 |
| Species | Caninized |
| Expression system | Mammalian cells |
| Purity | >85% |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Ranevetmab,NV-01,NGF, NGFB,anti-NGF, NGFB |
| Reference | PX-TA1448 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1-kappa |
| Clonality | Monoclonal Antibody |
Ranevetmab Biosimilar, also known as Anti-NGF or NGFB mAb, is a research grade antibody that specifically targets the nerve growth factor (NGF). This innovative therapeutic agent has shown promising results in preclinical studies and is currently in the process of clinical trials for various inflammatory and pain-related conditions.
Ranevetmab Biosimilar is a monoclonal antibody (mAb) that is produced using recombinant DNA technology. It is a fully humanized antibody, meaning that it is derived from human cells and has a structure similar to naturally occurring antibodies in the body. The antibody has a molecular weight of approximately 150 kDa and consists of two heavy chains and two light chains. These chains are linked together by disulfide bonds to form the characteristic Y-shaped structure of an antibody.
The main activity of Ranevetmab Biosimilar is its ability to bind to NGF with high affinity and specificity. NGF is a protein that plays a crucial role in the growth and survival of nerve cells. However, in certain conditions such as chronic pain and inflammatory diseases, an excess of NGF can lead to hyper-sensitization of nerve cells and contribute to the development of symptoms. Ranevetmab Biosimilar works by blocking the binding of NGF to its receptors, thereby preventing its harmful effects and providing therapeutic benefits.
In addition to its anti-NGF activity, Ranevetmab Biosimilar also has anti-inflammatory properties. It has been shown to inhibit the production of pro-inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-α) and interleukin-1 beta (IL-1β), which are known to play a role in various inflammatory conditions. This dual mechanism of action makes Ranevetmab Biosimilar a promising therapeutic agent for a wide range of diseases.
Ranevetmab Biosimilar is being developed for the treatment of various inflammatory and pain-related conditions, including osteoarthritis, rheumatoid arthritis, and chronic low back pain. These conditions are characterized by chronic pain, inflammation, and tissue damage, which can significantly impact the quality of life of patients.
In preclinical studies, Ranevetmab Biosimilar has shown promising results in reducing pain and inflammation in animal models of arthritis and neuropathic pain. It has also been shown to improve joint function and reduce cartilage damage in osteoarthritis models. These findings have paved the way for clinical trials to evaluate the safety and efficacy of Ranevetmab Biosimilar in human patients.
Besides its potential applications in human medicine, Ranevetmab Biosimilar also has potential uses in veterinary medicine. NGF has been implicated in various animal diseases, including osteoarthritis and chronic pain. Ranevetmab Biosimilar could potentially provide a safe and effective treatment option for these conditions in animals.
Ranevetmab Biosimilar, also known as Anti-NGF or NGFB mAb, is a research grade antibody with a promising potential for the treatment of various inflammatory and pain-related conditions. Its unique structure, high specificity, and dual mechanism of action make it a valuable therapeutic agent. With ongoing clinical trials and further research, Ranevetmab Biosimilar has the potential to improve the lives of patients suffering from these debilitating conditions.
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