The 17α-Hydroxyprogesterone Assay Kit is a sophisticated diagnostic tool used in neonatal screening programs. It employs time-resolved fluorescence technology to accurately measure 17α-Hydroxyprogesterone levels in dried blood spots, aiding in the early detection of congenital adrenal hyperplasia (CAH). The kit is designed for ease of use, reliability, and high sensitivity, making it an essential tool in clinical laboratories.

1. The kit features high sensitivity and specificity, ensuring accurate detection of 17α-Hydroxyprogesterone levels even at low concentrations. This is crucial for early diagnosis of CAH in newborns.
2. The composition includes a range of components such as calibrators, quality controls, and specific antibodies, all designed to work in harmony to provide precise and reliable results.
3. The primary use of the kit is in neonatal screening programs, where it helps in the early identification of CAH, allowing for timely intervention and management of the condition.

The 17α-Hydroxyprogesterone Assay Kit, also known as the 17-OHP Assay Kit, is a vital tool in neonatal screening. Its high sensitivity and specificity make it indispensable for the early detection of congenital adrenal hyperplasia. The kit's comprehensive components ensure reliable and accurate results, making it a trusted choice for clinical laboratories.

The 17α-Hydroxyprogesterone Assay Kit offers high sensitivity, specificity, and reliability in detecting 17α-Hydroxyprogesterone levels in neonatal blood samples. It is designed for ease of use and provides consistent results, making it a valuable tool in clinical diagnostics.

1. High Sensitivity: The kit can detect low concentrations of 17α-Hydroxyprogesterone, which is critical for early diagnosis of CAH.
2. Specificity: The use of specific antibodies ensures that the assay accurately measures 17α-Hydroxyprogesterone without cross-reactivity with other compounds.
3. Reliability: The inclusion of calibrators and quality controls ensures consistent and reproducible results.
4. Ease of Use: The kit is designed for straightforward operation, making it accessible for routine use in clinical laboratories.
5. Comprehensive Components: The kit includes all necessary components, from antibodies to microplate strips, ensuring a complete and efficient assay process.

The 17α-Hydroxyprogesterone Assay Kit stands out for its high sensitivity, specificity, and reliability. Its ease of use and comprehensive components make it an essential tool for clinical laboratories, particularly in neonatal screening programs.

The 17α-Hydroxyprogesterone Assay Kit is primarily used in neonatal screening for congenital adrenal hyperplasia (CAH). It provides accurate and reliable results, enabling early diagnosis and timely intervention.

1. Neonatal Screening: The kit is widely used in screening programs to detect CAH in newborns, allowing for early diagnosis and treatment.
2. Clinical Diagnostics: It is also used in clinical settings to monitor 17α-Hydroxyprogesterone levels in patients suspected of having CAH.
3. Research Applications: The kit is utilized in research studies to investigate the role of 17α-Hydroxyprogesterone in various endocrine disorders.
4. Quality Control: The kit's quality controls ensure that laboratories maintain high standards of accuracy and reliability in their diagnostic processes.
5. Public Health: By enabling early detection of CAH, the kit contributes to public health efforts to reduce the burden of this condition.

The 17α-Hydroxyprogesterone Assay Kit is a cornerstone in neonatal screening and clinical diagnostics. Its applications extend from routine screening to research, making it a versatile and invaluable tool in the fight against congenital adrenal hyperplasia.

When purchasing the 17α-Hydroxyprogesterone Assay Kit, consider factors such as product specifications, types, budget, and intended use to ensure the best fit for your laboratory's needs.

1. Product Specifications: Review the kit's sensitivity, specificity, and components to ensure it meets your laboratory's requirements.
2. Product Types: Choose between different kit formats based on your laboratory's throughput and workflow.
3. Budget: Consider the cost of the kit and any additional expenses, such as shipping and handling, to stay within your budget.
4. Intended Use: Ensure the kit is suitable for your specific applications, whether for neonatal screening, clinical diagnostics, or research.

Purchasing the 17α-Hydroxyprogesterone Assay Kit requires careful consideration of product specifications, types, budget, and intended use. By taking these factors into account, you can ensure that the kit meets your laboratory's needs and provides reliable results.

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

1. Storage Conditions: Store the kit components at the recommended temperatures to prevent degradation and ensure stability.
2. Handling: Follow proper laboratory protocols when handling the kit to avoid contamination and ensure accurate results.
3. Expiration Dates: Regularly check the expiration dates of the kit components and replace them as needed to maintain reliability.
4. Quality Control: Use the provided quality controls to monitor the performance of the assay and ensure consistent results.
5. Training: Ensure that laboratory personnel are adequately trained in the use of the kit to minimize errors and ensure accurate results.

The 17α-Hydroxyprogesterone Assay Kit requires careful handling and storage to maintain its integrity and ensure accurate results. By following proper protocols and regularly monitoring quality control, laboratories can maximize the kit's performance and reliability.