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Radioimmunoassay (RIA) to measure concentrations of substances (CAT#: STEM-MB-0171-WXH)

Introduction

Radioimmunoassay (RIA) technology is a new technology for in vitro determination of ultra-trace substances that combines the high sensitivity and accuracy of radioisotope measurement with the specificity of antigen-antibody reactions.<br />Radioimmunoassay generally uses competitive binding assay technology. The basic principle is that the radiolabeled antigen and the tested antigen (or standard substance) undergo a reversible competitive binding reaction to a limited specific antibody, and the amount of the finally formed radioactive antigen-antibody complex is negatively correlated with the content of the tested substance. When the amount of antibody is fixed, the formation of immune complexes is restricted by the amount of antigen to be tested. The advantages of the RIA method are sensitivity, specificity, simplicity, and small sample volume, and can often be measured to picomolar.




Applications

• Detection of Drug Intoxication and Drug Metabolism
• Endocrinology: Study the physiological and pharmacological effects of hormones, which are currently more often used to study the mechanism of hormone binding to receptors.
• Determination of insulin, growth hormone, parathyroid hormone, angiotensin, etc.
• Infectious Diseases: Widely used in subtyping assays for hepatitis B antigens.
• Clinical Immunology: Determination of Immunoglobulin G, Immunoglobulin E, and Anti-DNA Antibodies
• Oncology: Determination of carcinoembryonic antigen, plasminogen, folic acid, vitamin B12, fibrinogen and fibrin degradation products, effective primary screening and tracking of release of human chorionic gonadotropin, carcinoembryonic hormone after surgery Antigens and alpha-fetoprotein tumors

Procedure

1. Reaction of radioisotope-labeled antigen with antibody
2. Separation of labeled antigen-antibody complexes (B) and free labeled antigen (F)
3. Measurement of radioactivity using scintillation counter