The 17α-Hydroxyprogesterone (17α-OHP) Assay Kit is a state-of-the-art diagnostic tool utilizing magnetic particle chemiluminescence technology. It offers high sensitivity and specificity for measuring 17α-OHP levels in human serum, making it an essential tool for diagnosing and monitoring adrenal and gonadal disorders. The kit is designed for ease of use, with a robust and reliable performance that ensures accurate results in clinical settings.
1. The kit features advanced chemiluminescence technology, which provides high sensitivity and a broad dynamic range for detecting 17α-OHP levels. This ensures precise measurements even at low concentrations.
2. The composition includes magnetic separation reagents, calibrators, and quality controls, all of which are optimized for stability and performance. The reagents are designed to minimize interference and ensure consistent results.
3. The primary use of this kit is in the diagnosis and monitoring of adrenal and gonadal disorders, particularly congenital adrenal hyperplasia (CAH). It is also used in research settings to study steroid hormone metabolism.
The 17α-OHP Assay Kit is a reliable and efficient tool for measuring 17α-hydroxyprogesterone levels in human serum. Its advanced chemiluminescence technology and well-optimized reagents make it a preferred choice for clinical diagnostics and research. Whether you're diagnosing CAH or studying steroid metabolism, this kit delivers consistent and accurate results.
The 17α-OHP Assay Kit offers high sensitivity, specificity, and a broad dynamic range for detecting 17α-OHP levels in human serum. It is designed for ease of use and reliable performance in clinical diagnostics.
1. High Sensitivity: The kit can detect low concentrations of 17α-OHP with high precision, making it suitable for early diagnosis and monitoring of adrenal disorders.
2. Broad Dynamic Range: It provides accurate measurements across a wide range of 17α-OHP concentrations, ensuring reliable results in various clinical scenarios.
3. Stability: The reagents are formulated for long-term stability, reducing the need for frequent recalibration and ensuring consistent performance over time.
4. Ease of Use: The kit is designed for straightforward operation, with clear instructions and minimal hands-on time required.
5. Clinical Utility: It is widely used in the diagnosis and management of congenital adrenal hyperplasia (CAH) and other adrenal and gonadal disorders.
The 17α-OHP Assay Kit stands out for its high sensitivity, broad dynamic range, and ease of use. Its stability and clinical utility make it an indispensable tool for diagnosing and monitoring adrenal and gonadal disorders. Whether in a busy clinical lab or a research setting, this kit delivers reliable and accurate results.
The 17α-OHP Assay Kit is primarily used in clinical diagnostics for the quantitative measurement of 17α-hydroxyprogesterone in human serum. It is essential for diagnosing and monitoring adrenal and gonadal disorders.
1. Diagnosis of Congenital Adrenal Hyperplasia (CAH): The kit is widely used to measure 17α-OHP levels, which are elevated in patients with CAH, aiding in early diagnosis and management.
2. Monitoring Adrenal Function: It is used to assess adrenal function in patients with suspected adrenal insufficiency or other adrenal disorders.
3. Research Applications: The kit is also used in research settings to study steroid hormone metabolism and the role of 17α-OHP in various physiological processes.
4. Neonatal Screening: It is employed in neonatal screening programs to detect elevated 17α-OHP levels, which may indicate CAH or other adrenal disorders.
5. Hormonal Imbalance Studies: The kit is used to investigate hormonal imbalances and their impact on reproductive health and overall well-being.
The 17α-OHP Assay Kit is a versatile tool in clinical diagnostics, essential for diagnosing and monitoring adrenal and gonadal disorders. Its applications extend to research, neonatal screening, and hormonal imbalance studies, making it a valuable asset in both clinical and research settings.
When purchasing the 17α-OHP Assay Kit, consider factors such as product specifications, intended use, budget, and application scenarios to ensure it meets your diagnostic needs.
1. Product Specifications: Evaluate the kit's sensitivity, dynamic range, and stability to ensure it meets your laboratory's requirements.
2. Product Type: Choose between different kit formats (e.g., single-use vs. bulk) based on your lab's workflow and testing volume.
3. Budget Considerations: Assess the cost-effectiveness of the kit, including the price per test and any additional costs for calibrators or quality controls.
4. Application Scenarios: Consider the specific clinical or research applications for which the kit will be used, ensuring it is suitable for your intended use.
Purchasing the 17α-OHP Assay Kit requires careful consideration of product specifications, type, budget, and application scenarios. By evaluating these factors, you can ensure that the kit meets your diagnostic needs and delivers reliable results in your clinical or research setting.
Proper handling and storage of the 17α-OHP Assay Kit are essential to ensure accurate results and maintain the integrity of the reagents.
1. Storage Conditions: Store the kit at the recommended temperature to maintain reagent stability and performance.
2. Handling Precautions: Follow proper laboratory procedures to avoid contamination and ensure accurate results.
3. Reagent Preparation: Prepare reagents according to the manufacturer's instructions to ensure optimal performance.
4. Calibration and Quality Control: Regularly calibrate the assay and run quality controls to verify the accuracy and precision of the results.
5. Disposal: Dispose of used reagents and materials according to local regulations and laboratory safety protocols.
The 17α-OHP Assay Kit requires careful handling and storage to ensure accurate and reliable results. By following proper procedures for storage, handling, reagent preparation, and disposal, you can maintain the integrity of the kit and achieve consistent performance in your clinical or research applications.
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