The 17α-Hydroxyprogesterone Assay Kit is a state-of-the-art diagnostic tool designed for the accurate measurement of 17α-OHP levels in human serum or plasma. Utilizing chemiluminescence technology, this kit offers high sensitivity and specificity, making it an essential tool for clinicians in the diagnosis and management of adrenal disorders.

1. The kit features advanced chemiluminescence technology, ensuring high precision and reliability in detecting 17α-OHP levels. Its robust design minimizes interference, providing consistent results across various clinical settings.
2. The kit comprises multiple components, including reagents, calibrators, and optional controls. Each component is meticulously formulated to ensure optimal performance, with buffers and stabilizers like ProClin300 enhancing the kit's stability and shelf life.
3. Clinically, the kit is indispensable for diagnosing adrenal cortex disorders, particularly congenital adrenal hyperplasia. It aids in monitoring treatment efficacy and disease progression, offering clinicians valuable insights into patient health.

The 17α-Hydroxyprogesterone Assay Kit, also known as the 17α-OHP Kit, is a reliable and precise diagnostic tool. Its advanced chemiluminescence technology and comprehensive components make it a vital resource for clinicians, particularly in the diagnosis and management of adrenal disorders.

The 17α-Hydroxyprogesterone Assay Kit offers high sensitivity, specificity, and reliability in detecting 17α-OHP levels. Its advanced chemiluminescence technology ensures accurate results, making it a trusted tool in clinical diagnostics.

1. High Sensitivity: The kit's chemiluminescence technology detects even low concentrations of 17α-OHP, ensuring accurate diagnosis of adrenal disorders.
2. Specificity: The use of specific antibodies minimizes cross-reactivity, providing precise measurements of 17α-OHP levels.
3. Reliability: The kit's robust design and quality components ensure consistent performance across different clinical settings.
4. Ease of Use: The kit is designed for straightforward operation, with clear instructions and minimal preparation required.
5. Comprehensive Components: The inclusion of calibrators and optional controls enhances the kit's accuracy and reliability.

The 17α-Hydroxyprogesterone Assay Kit stands out for its high sensitivity, specificity, and reliability. Its advanced technology and user-friendly design make it an essential tool for clinicians, ensuring accurate and consistent results in the diagnosis of adrenal disorders.

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

1. Diagnosis of Congenital Adrenal Hyperplasia: The kit is crucial for identifying elevated 17α-OHP levels, a hallmark of this condition.
2. Monitoring Treatment Efficacy: Clinicians use the kit to track 17α-OHP levels during treatment, ensuring optimal therapeutic outcomes.
3. Screening Newborns: The kit is employed in neonatal screening programs to detect congenital adrenal hyperplasia early.
4. Research Applications: Researchers utilize the kit in studies exploring adrenal function and related disorders.
5. Routine Clinical Testing: The kit is integrated into routine diagnostic workflows, providing reliable results for patient care.

The 17α-Hydroxyprogesterone Assay Kit is a versatile tool in clinical diagnostics, playing a key role in the diagnosis, monitoring, and research of adrenal disorders. Its reliability and precision make it indispensable in both clinical and research settings.

When purchasing the 17α-Hydroxyprogesterone Assay Kit, consider factors such as product specifications, types, budget, and intended use to ensure it meets your clinical needs.

1. Product Specifications: Evaluate the kit's sensitivity, specificity, and component details to ensure it aligns with your diagnostic requirements.
2. Product Types: Choose between standard and optional control kits based on your laboratory's needs and testing protocols.
3. Budget Considerations: Assess the cost-effectiveness of the kit, considering its performance and the volume of tests you plan to conduct.
4. Usage Scenarios: Ensure the kit is suitable for your clinical setting, whether for routine diagnostics, neonatal screening, or research purposes.

Selecting the right 17α-Hydroxyprogesterone Assay Kit involves careful consideration of its specifications, types, cost, and intended use. By evaluating these factors, you can ensure the kit meets your clinical needs and delivers reliable results.

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

1. Storage Conditions: Store the kit at the recommended temperature to preserve the stability of its components.
2. Handling Procedures: Follow the manufacturer's instructions for handling reagents and samples to avoid contamination and ensure accurate results.
3. Expiry Dates: Regularly check the kit's expiration date and avoid using expired components.
4. Safety Measures: Use appropriate personal protective equipment when handling the kit to prevent exposure to hazardous materials.
5. Quality Control: Regularly perform quality control tests to verify the kit's performance and ensure reliable results.

To maximize the performance and accuracy of the 17α-Hydroxyprogesterone Assay Kit, adhere to proper storage, handling, and safety protocols. Regular quality control checks and attention to expiration dates are crucial for maintaining the kit's reliability in clinical diagnostics.