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| Size | 96T |
|---|---|
| Brand | ProteoGenix |
| Product type | Elisa assay kits |
| Product name | Elotuzumab ELISA Kit |
|---|---|
| Delivery condition | Blue ice (+4°C) |
| Delivery lead time in business days | 3-5 days if in stocks, 3-5 weeks if production is needed |
| Storage condition | 4°C for short term (1 week), store at -20°C to -80°C for long term(1 year); Avoid repeated freeze-thaw cycles |
| Brand | ProteoGenix |
| Note | For research use only. |
| Immunogen | Elotuzumab |
| Assay type | Quantitative |
| Detection method | Colorimetric |
| Recovery | 80-120% |
Elotuzumab is a humanized monoclonal antibody that targets the SLAMF7 (signaling lymphocytic activation molecule family member 7) protein, also known as CS1 (CD2 subset 1). This protein is highly expressed on the surface of multiple myeloma cells and is involved in the proliferation and survival of these cancerous cells. Elotuzumab has been approved by the FDA for the treatment of multiple myeloma in combination with other anti- cancer drugs. The development of the Elotuzumab ELISA Kit has enabled researchers to accurately measure the levels of this protein in biological samples, aiding in the understanding of its role in multiple myeloma and the effectiveness of Elotuzumab as a therapeutic target.
Elotuzumab is a recombinant humanized IgG1 monoclonal antibody with a molecular weight of approximately 149 kDa. It is composed of two identical heavy chains and two identical light chains, each containing a variable region and a constant region. The variable region is responsible for binding to the SLAMF7 protein, while the constant region is involved in effector functions such as complement-dependent cytotoxicity and antibody-dependent cellular cytotoxicity. The humanization of Elotuzumab has reduced its immunogenicity, making it more suitable for therapeutic use.
The primary mechanism of action of Elotuzumab is through its binding to the SLAMF7 protein on the surface of multiple myeloma cells. This binding leads to the activation of natural killer (NK) cells and macrophages, which then target and kill the cancerous cells. Elotuzumab also has a direct anti-proliferative effect on multiple myeloma cells by inhibiting the interaction between SLAMF7 and its ligand, CD47. This results in decreased survival and proliferation of the cancerous cells.
The Elotuzumab ELISA Kit is a valuable tool for researchers studying the role of SLAMF7 in multiple myeloma and the effectiveness of Elotuzumab as a therapeutic target. This kit allows for the accurate measurement of SLAMF7 levels in various biological samples, including serum, plasma, and cell lysates. It can also be used to quantify the amount of Elotuzumab in patient samples, providing information on drug levels and potential drug resistance.
The development of Elotuzumab as a therapeutic target has shown promising results in the treatment of multiple myeloma. In clinical trials, the combination of Elotuzumab with other anti- cancer drugs has demonstrated improved outcomes, including increased progression-free survival and overall response rates, compared to standard therapy. Additionally, the use of Elotuzumab has shown a favorable safety profile, with minimal side effects reported.
Besides its application in clinical settings, the Elotuzumab ELISA Kit has also been widely used in research studies. By accurately measuring SLAMF7 levels, researchers can better understand the role of this protein in multiple myeloma and its potential as a therapeutic target. The kit has also been used to investigate the relationship between SLAMF7 and other proteins involved in the pathogenesis of multiple myeloma, providing insights into potential combination therapies.
The development of the Elotuzumab ELISA Kit has been a crucial step in the study and treatment of multiple myeloma. This kit enables the accurate measurement of SLAMF7 levels, providing valuable information on its role in the disease and the effectiveness of Elotuzumab as a therapeutic target. With ongoing research and clinical trials, Elotuzumab has the potential to significantly improve outcomes for patients
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