The 17α-Hydroxyprogesterone Assay Kit is a sophisticated diagnostic tool used in clinical laboratories to measure the levels of 17α-hydroxyprogesterone in human serum. This kit employs a chemiluminescent immunoassay method, which is known for its high sensitivity and specificity. It is an essential tool for diagnosing adrenal cortex disorders, providing accurate and reliable results.

1. The kit features a highly sensitive chemiluminescent immunoassay method, ensuring precise measurement of 17α-hydroxyprogesterone levels. This method is known for its low detection limit and high specificity, making it ideal for clinical diagnostics.
2. The kit consists of magnetic bead-coated particles, enzyme-labeled conjugates, antibody working solution, and optional calibrators. Each component is carefully formulated to ensure stability and accuracy in the assay process.
3. The primary use of this kit is in the clinical diagnosis of adrenal cortex disorders. It provides quantitative results that are crucial for the accurate assessment of 17α-hydroxyprogesterone levels, aiding in the diagnosis and management of these conditions.

The 17α-Hydroxyprogesterone Assay Kit, also known as the 17α-OHP Kit, is a vital diagnostic tool in clinical laboratories. Its high sensitivity and specificity make it an indispensable resource for diagnosing adrenal cortex disorders. The kit's components are meticulously designed to ensure accurate and reliable results, making it a trusted choice for healthcare professionals.

The 17α-Hydroxyprogesterone Assay Kit offers high sensitivity and specificity in measuring 17α-hydroxyprogesterone levels, making it a reliable tool for clinical diagnostics.

1. The kit utilizes a chemiluminescent immunoassay method, which provides high sensitivity and specificity in detecting 17α-hydroxyprogesterone levels.
2. The magnetic bead-coated particles ensure efficient binding and separation of the target analyte, enhancing the accuracy of the assay.
3. The enzyme-labeled conjugates are designed to provide a stable and detectable signal, ensuring reliable results.
4. The antibody working solution is optimized for high affinity and specificity, ensuring accurate detection of 17α-hydroxyprogesterone.
5. The optional calibrators allow for precise quantification of 17α-hydroxyprogesterone levels, ensuring the accuracy of the assay results.

The 17α-Hydroxyprogesterone Assay Kit is a highly reliable diagnostic tool, offering precise measurement of 17α-hydroxyprogesterone levels. Its advanced features, including the chemiluminescent immunoassay method and optimized components, make it an essential resource for clinical laboratories.

The 17α-Hydroxyprogesterone Assay Kit is widely used in clinical settings for the diagnosis and management of adrenal cortex disorders.

1. The kit is used in the diagnosis of congenital adrenal hyperplasia (CAH), a condition caused by the deficiency of enzymes involved in cortisol synthesis.
2. It is also used in the diagnosis of other adrenal cortex disorders, such as Cushing's syndrome and adrenal insufficiency.
3. The kit provides quantitative results that are crucial for the accurate assessment of 17α-hydroxyprogesterone levels, aiding in the diagnosis and management of these conditions.
4. The kit is used in monitoring the effectiveness of treatment in patients with adrenal cortex disorders, providing valuable information for adjusting treatment plans.
5. The kit is also used in research settings to study the role of 17α-hydroxyprogesterone in various physiological and pathological processes.

The 17α-Hydroxyprogesterone Assay Kit is an essential tool in the clinical diagnosis and management of adrenal cortex disorders. Its ability to provide accurate and reliable results makes it a valuable resource for healthcare professionals and researchers alike.

The 17α-Hydroxyprogesterone Assay Kit is a specialized diagnostic tool, and its procurement requires careful consideration of various factors.

1. Product parameters: When purchasing the kit, it is important to consider the sensitivity, specificity, and detection range of the assay to ensure it meets the diagnostic needs.
2. Product type: The kit is available in different formats, including single-use and multi-use kits. The choice depends on the volume of testing required.
3. Procurement budget: The cost of the kit should be considered in relation to the budget and the expected volume of testing.
4. Usage scenarios: The kit is suitable for use in clinical laboratories, research institutions, and hospitals. The choice of kit should align with the specific needs of the institution.

The procurement of the 17α-Hydroxyprogesterone Assay Kit requires careful consideration of various factors, including product parameters, type, budget, and usage scenarios. Ensuring that the kit meets the specific needs of the institution is crucial for its effective use in clinical diagnostics.

Proper handling and storage of the 17α-Hydroxyprogesterone Assay Kit are essential to ensure accurate and reliable results.

1. The kit should be stored at the recommended temperature to maintain the stability of the components.
2. Proper handling of the magnetic bead-coated particles is crucial to avoid contamination and ensure accurate results.
3. The enzyme-labeled conjugates should be protected from light to prevent degradation.
4. The antibody working solution should be used within the specified period to ensure optimal performance.
5. Regular calibration of the assay using the provided calibrators is essential to maintain the accuracy of the results.

The 17α-Hydroxyprogesterone Assay Kit requires careful handling and storage to ensure accurate and reliable results. Proper storage, handling, and calibration are essential to maintain the performance of the kit and ensure the accuracy of the diagnostic results.