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| Size | 100ug, 1MG |
|---|---|
| Isotype | F(ab')2, Fab / Fab2 mix, IgG1-ndF(ab')2-G1-kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Tecnemab Biosimilar - Anti-CSPG4, HMW-MAA, CD3E, ERBB2, toxin mAb - Research Grade |
|---|---|
| Species | Mus musculus |
| 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 | Clostridium perfringens,225.28S,Tecnemab-K-1,3-4D10,4D5-8 and UCHT1,BsF(ab')2 v1,F(ab')2 trastusumab/humanized UCHT1-v1,F(ab')2 4D5-8/UCHT1-v1,CSPG4, HMW-MAA, CD3E, ERBB2, toxin,anti-CSPG4, HMW-MAA, CD3E, ERBB2, toxin |
| Reference | PX-TA1100 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | F(ab')2, Fab / Fab2 mix, IgG1-nd, F(ab')2-G1-kappa |
| Clonality | Monoclonal Antibody |
Tecnemab Biosimilar is a type of monoclonal antibody (mAb) that has been designed to target and bind to specific proteins known as CSPG4, HMW-MAA, CD3E, ERBB2, and toxin. This biosimilar is currently in the research grade stage and has shown promising potential as a therapeutic agent for various diseases.
Tecnemab Biosimilar is a recombinant humanized IgG1 monoclonal antibody. It is composed of two heavy chains and two light chains, each containing a variable region and a constant region. The variable regions of the antibody are responsible for binding to the target proteins, while the constant regions provide stability and effector functions.
Tecnemab Biosimilar has been designed to target and bind to four different proteins: CSPG4, HMW-MAA, CD3E, and ERBB2. These proteins are known to play important roles in various diseases, making them potential therapeutic targets.
CSPG4 is a cell surface protein that is overexpressed in several types of cancer, including melanoma, breast cancer, and lung cancer. It is involved in tumor growth, invasion, and metastasis. By targeting CSPG4, Tecnemab Biosimilar can potentially inhibit the growth and spread of cancer cells.
HMW-MAA is a glycoprotein that is also overexpressed in various types of cancer. It is involved in promoting tumor growth and angiogenesis. By binding to HMW-MAA, Tecnemab Biosimilar can potentially block its activity and inhibit tumor growth.
CD3E is a protein found on the surface of T-cells, a type of immune cell. By targeting CD3E, Tecnemab Biosimilar can potentially modulate the activity of T-cells and enhance the immune response against cancer cells.
ERBB2, also known as HER2, is a protein that is overexpressed in breast cancer. It is involved in promoting cell growth and survival. By targeting ERBB2, Tecnemab Biosimilar can potentially inhibit the growth and survival of breast cancer cells.
In addition to targeting these four proteins, Tecnemab Biosimilar also contains a toxin, which can potentially enhance its anti-tumor activity. The toxin is designed to be released upon binding to the target proteins, leading to cell death.
Tecnemab Biosimilar has shown promising results in preclinical studies for the treatment of various types of cancer, including melanoma, breast cancer, and lung cancer. It has also shown potential for use in combination with other therapies, such as chemotherapy and targeted therapy.
The biosimilar is currently in the research grade stage, and further studies are needed to determine its safety and efficacy in humans. If successful, it could potentially become a valuable therapeutic option for patients with cancer.
Tecnemab Biosimilar is a recombinant humanized monoclonal antibody that has been designed to target and bind to specific proteins involved in cancer growth and progression. Its unique structure and ability to target multiple proteins make it a promising therapeutic agent for various types of cancer. Further research and clinical trials are needed to fully evaluate its potential as a treatment option for patients with cancer.
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