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Ifabotuzumab ELISA Kit

Reference: KPTX218
Brand

ProteoGenix

Product type

Elisa assay kits

Size

96T

Product nameIfabotuzumab ELISA Kit
Delivery conditionBlue ice (+4°)
Storage conditionThe 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.
BrandProteoGenix
Size96T
ReferenceKPTX218
NoteFor research use only.
Sample typePlasma, Serum
ImmunogenIfabotuzumab

Description of Ifabotuzumab ELISA Kit

Introduction

Ifabotuzumab is a monoclonal antibody that has shown promise as a therapeutic target for various types of cancer. The use of Ifabotuzumab ELISA Kit allows for the detection and measurement of this antibody in biological samples, providing valuable information for researchers and clinicians. In this article, we will explore the structure, activity, and potential applications of Ifabotuzumab ELISA Kit in the field of oncology.

Structure of Ifabotuzumab

Ifabotuzumab is a fully humanized monoclonal antibody that targets the extracellular domain of the EphA3 receptor. This receptor is overexpressed in various types of cancer cells, making it an attractive therapeutic target. The antibody is composed of two heavy chains and two light chains, each with a specific amino acid sequence. The binding site of Ifabotuzumab is located on the variable region of the heavy chain, allowing for specific and selective targeting of the EphA3 receptor.

Activity of Ifabotuzumab

The main mechanism of action of Ifabotuzumab is through the inhibition of the EphA3 receptor. This receptor is involved in cell signaling pathways that promote cell growth, survival, and migration. By binding to the receptor, Ifabotuzumab blocks these pathways and prevents cancer cells from proliferating and spreading. Additionally, Ifabotuzumab has been shown to induce antibody-dependent cell-mediated cytotoxicity (ADCC), where immune cells recognize and kill cancer cells that are bound by the antibody.

Application of Ifabotuzumab ELISA Kit

The Ifabotuzumab ELISA Kit is a valuable tool for researchers and clinicians in the field of oncology. It allows for the detection and measurement of Ifabotuzumab in various biological samples, such as serum, plasma, and tissue extracts. This information can be used to monitor the levels of Ifabotuzumab in patients receiving treatment, as well as to assess the efficacy of the antibody in clinical trials. The ELISA Kit can also be used to screen for potential responders to Ifabotuzumab therapy, as well as to identify patients who may benefit from combination therapy with other targeted agents.

Detection of Ifabotuzumab in Biological Samples

The Ifabotuzumab ELISA Kit utilizes a sandwich immunoassay format, where the antibody is captured by a specific coating on the plate and then detected by a secondary antibody labeled with an enzyme. The amount of enzyme activity is directly proportional to the amount of Ifabotuzumab present in the sample, allowing for accurate and sensitive measurement. This method is highly specific for Ifabotuzumab and does not cross-react with other antibodies or proteins, ensuring reliable results.

Monitoring of Ifabotuzumab Therapy

The Ifabotuzumab ELISA Kit can be used to monitor the levels of Ifabotuzumab in patients receiving treatment. This information can help clinicians adjust the dose or frequency of administration to optimize the therapeutic effect. It can also be used to assess the pharmacokinetics of Ifabotuzumab, providing insights into its distribution and elimination from the body. Monitoring the levels of Ifabotuzumab can also help identify patients who may require a higher or lower dose of the antibody to achieve a therapeutic response.

Potential for Combination Therapy

The Ifabotuzumab ELISA Kit can also be used to identify patients who may benefit from combination therapy with other targeted agents. By measuring the levels of Ifabotuzumab in combination with other antibodies or drugs, researchers can determine the optimal combination and dosing regimen for maximum efficacy. This approach has the potential to improve treatment outcomes and overcome resistance to single-agent therapy.

Conclusion

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