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View ProductsBrand | ProteoGenix |
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Product type | Elisa assay kits |
Size | 96T |
Product name | Belantamab ELISA Kit |
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Delivery condition | Blue ice (+4°) |
Storage condition | The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 10% prior to the expiration date under appropriate storage condition. |
Brand | ProteoGenix |
Size | 96T |
Reference | KPTX236 |
Note | For research use only. |
Sample type | Plasma, Serum |
Immunogen | Belantamab |
The Belantamab ELISA Kit is a diagnostic tool used to measure the levels of belantamab mafodotin in biological samples. Belantamab mafodotin is a monoclonal antibody-drug conjugate (ADC) that targets the B-cell maturation antigen (BCMA), a protein found on the surface of multiple myeloma cells. The kit is designed to detect and quantify the presence of belantamab mafodotin in serum, plasma, or cell culture supernatants.
The Belantamab ELISA Kit is composed of several components, including a microplate coated with a specific antibody against belantamab mafodotin, a set of standards with known concentrations of the drug, and reagents for sample preparation and detection. The microplate is made of polystyrene and has 96 wells, each capable of holding a small volume of sample. The specific antibody used in the kit is highly sensitive and specific for belantamab mafodotin, ensuring accurate and reliable results.
Belantamab mafodotin is a novel ADC that combines the targeting specificity of a monoclonal antibody with the cytotoxic effects of a small molecule drug. The antibody component of belantamab mafodotin binds to BCMA on the surface of myeloma cells, while the drug component, monomethyl auristatin F (MMAF), induces cell death by disrupting microtubule formation. This dual mechanism of action makes belantamab mafodotin a potent and selective therapeutic agent for the treatment of multiple myeloma.
Belantamab mafodotin has shown promising results in preclinical studies, with high efficacy against multiple myeloma cells and minimal toxicity to normal cells. In clinical trials, belantamab mafodotin has demonstrated significant anti-tumor activity in patients with relapsed or refractory multiple myeloma, leading to its recent approval by the US Food and Drug Administration (FDA) for this indication. Ongoing studies are also evaluating the potential of belantamab mafodotin in other types of cancer that express BCMA, such as non-Hodgkin’s lymphoma and solid tumors.
The Belantamab ELISA Kit has several applications in the field of oncology, particularly in the development and monitoring of belantamab mafodotin-based therapies. The kit can be used to measure the levels of belantamab mafodotin in patient samples, providing valuable information on drug exposure and response to treatment. This can help clinicians optimize dosing regimens and monitor treatment efficacy, as well as detect potential adverse effects.
The Belantamab ELISA Kit can also be used in research settings to study the pharmacokinetics and pharmacodynamics of belantamab mafodotin. By measuring drug levels in different biological samples, researchers can gain insight into the distribution, metabolism, and elimination of belantamab mafodotin in the body. This information can inform the development of new ADCs and improve the understanding of ADC-related toxicity.
In addition, the Belantamab ELISA Kit can be used to screen potential drug candidates or assess the stability of belantamab mafodotin in different formulations. This can help pharmaceutical companies select the most promising candidates for further development and ensure the quality and consistency of the final product.
The Belantamab ELISA Kit is a valuable tool for the detection and quantification of belantamab mafodotin, a promising ADC with high potential for the treatment of multiple myeloma and other BCMA-expressing cancers. Its unique structure and mechanism of
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