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View ProductsBrand | ProteoGenix |
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Product type | Elisa assay kits |
Size | 96T |
Product name | Cetrelimab 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 | KPTX251 |
Note | For research use only. |
Sample type | Plasma, Serum |
Immunogen | Cetrelimab |
The Cetrelimab ELISA Kit is a highly sensitive and specific assay designed for the detection of cetrelimab, a monoclonal antibody used as a therapeutic agent in the treatment of cancer. This kit is an essential tool for researchers and clinicians to monitor the levels of cetrelimab in patient samples, providing valuable insights into its structure, activity, and application.
Cetrelimab, also known as REGN2810, is a fully human monoclonal antibody that targets the programmed cell death protein 1 (PD-1). It is composed of two heavy chains and two light chains, linked together by disulfide bonds. The heavy chains consist of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH), while the light chains have two constant domains (CL and CL1) and one variable domain (VL).
The variable domains of cetrelimab are responsible for its specificity and binding to PD-1, while the constant domains provide stability and effector functions. The heavy chains contain a hinge region that allows for flexibility and optimal binding to PD-1 on the surface of T cells. The overall structure of cetrelimab is crucial for its activity and therapeutic efficacy.
Cetrelimab works by blocking the interaction between PD-1 and its ligands, programmed death-ligand 1 (PD-L1) and 2 (PD-L2). PD-1 is an immune checkpoint receptor expressed on T cells, and its activation leads to the suppression of T cell activity, allowing cancer cells to evade the immune system. By binding to PD-1, cetrelimab prevents this suppression and restores the anti-tumor activity of T cells.
The activity of cetrelimab has been demonstrated in various pre-clinical and clinical studies. In a phase 1 trial, cetrelimab showed promising results in patients with advanced solid tumors, with an overall response rate of 34%. It has also been approved by the FDA for the treatment of advanced cutaneous squamous cell carcinoma, a type of skin cancer.
The Cetrelimab ELISA Kit is a valuable tool for the detection and quantification of cetrelimab in various biological samples, including serum, plasma, and cell culture supernatants. This kit utilizes a sandwich ELISA format, where cetrelimab is captured by a specific anti-cetrelimab antibody coated on a microplate and detected by a second anti-cetrelimab antibody conjugated to an enzyme.
The sensitivity of this assay allows for the detection of cetrelimab at levels as low as 0.1 ng/mL, making it suitable for monitoring the pharmacokinetics of cetrelimab in patients. It also has a wide dynamic range, ensuring accurate detection of cetrelimab in both high and low concentration samples.
In addition to its use in clinical settings, the Cetrelimab ELISA Kit has also been utilized in research studies to investigate the pharmacokinetics and pharmacodynamics of cetrelimab in various animal models. This has provided valuable insights into the mechanism of action and potential side effects of cetrelimab.
The Cetrelimab ELISA Kit is an essential tool for the detection and quantification of cetrelimab, a monoclonal antibody used as a therapeutic agent in the treatment of cancer. Its high sensitivity, specificity, and wide dynamic range make it a valuable tool for researchers and clinicians to monitor the levels of cetrelimab in patient samples. Understanding the structure, activity, and application of cetrelimab is crucial for its successful use
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