The 17α-Hydroxyprogesterone Assay Kit (Time-Resolved Fluorescence Method) is a highly sensitive and specific diagnostic tool used in clinical laboratories. It employs advanced time-resolved fluorescence technology to accurately measure 17α-hydroxyprogesterone levels in neonatal blood samples. This kit is essential for early detection of congenital adrenal hyperplasia, a condition that can lead to severe health complications if not diagnosed and treated promptly.

1. The kit features a robust design with high precision and reproducibility, ensuring reliable results in clinical settings. Its time-resolved fluorescence method minimizes background noise, enhancing sensitivity.
2. The components include calibrators, quality controls, and specialized reagents such as europium-labeled tracer and rabbit polyclonal antiserum. These are carefully formulated to ensure accurate and consistent performance.
3. The primary application of this kit is in newborn screening programs, where it plays a critical role in identifying infants at risk for congenital adrenal hyperplasia. Early detection allows for timely intervention and management.

The 17α-Hydroxyprogesterone Assay Kit is a vital tool in neonatal screening, offering precision and reliability. Its advanced technology and comprehensive components make it indispensable for early detection of congenital adrenal hyperplasia, ensuring better health outcomes for newborns.

This kit offers high sensitivity and specificity for measuring 17α-hydroxyprogesterone levels, utilizing time-resolved fluorescence technology to ensure accurate and reliable results.

1. The kit employs a time-resolved fluorescence method, which significantly reduces background interference, enhancing the accuracy of measurements.
2. It includes a comprehensive set of components, such as calibrators and quality controls, ensuring consistent performance across different batches.
3. The europium-labeled tracer and rabbit polyclonal antiserum are key reagents that contribute to the kit's high specificity and sensitivity.
4. The anti-rabbit IgG microplate strips are designed for easy handling and efficient binding, streamlining the assay process.
5. The kit is validated for use in newborn screening programs, providing reliable results for early detection of congenital adrenal hyperplasia.

The 17α-Hydroxyprogesterone Assay Kit stands out for its advanced technology and reliable performance. Its components and design ensure accurate measurements, making it a trusted choice for neonatal screening.

This kit is widely used in clinical laboratories for newborn screening, specifically for the early detection of congenital adrenal hyperplasia (CAH).

1. The kit is integral to newborn screening programs, where it helps identify infants with elevated 17α-hydroxyprogesterone levels, a marker for CAH.
2. It is used in conjunction with blood spot samples collected on filter paper, making it convenient for large-scale screening initiatives.
3. The kit's high sensitivity allows for the detection of even low levels of 17α-hydroxyprogesterone, ensuring early diagnosis and intervention.
4. Clinical laboratories rely on this kit for its reproducibility and accuracy, which are critical for reliable screening results.
5. The kit's application extends to research studies focused on understanding the prevalence and management of CAH in different populations.

The 17α-Hydroxyprogesterone Assay Kit is a cornerstone of newborn screening programs, enabling early detection of congenital adrenal hyperplasia. Its clinical applications are vital for improving infant health outcomes.

When purchasing this kit, consider factors such as product specifications, types, budget, and intended use to ensure it meets your laboratory's needs.

1. Evaluate the product parameters, including sensitivity, specificity, and reproducibility, to ensure it aligns with your laboratory's requirements.
2. Choose the appropriate kit type based on your screening volume and laboratory capabilities. Bulk purchases may offer cost savings for high-throughput labs.
3. Establish a clear budget, factoring in not only the initial cost but also long-term expenses such as reagent replenishment and maintenance.
4. Consider the intended use, such as newborn screening or research, to select a kit that best suits your application.

Purchasing the 17α-Hydroxyprogesterone Assay Kit requires careful consideration of parameters, types, and budget. Ensuring alignment with your laboratory's needs will optimize its utility and cost-effectiveness.

Proper handling and storage of the kit components are essential to maintain their integrity and ensure accurate results.

1. Store the kit at the recommended temperature to preserve the stability of the reagents and prevent degradation.
2. Follow the manufacturer's instructions for handling and disposal of reagents to avoid contamination and ensure safety.
3. Use the kit within its expiration date to guarantee optimal performance and reliability of results.
4. Ensure proper calibration of equipment and adherence to assay protocols to minimize errors and variability.
5. Train laboratory personnel on the correct use of the kit to maintain consistency and accuracy in testing.

Adhering to proper storage, handling, and usage guidelines is crucial for the 17α-Hydroxyprogesterone Assay Kit. These precautions ensure reliable results and extend the kit's lifespan, making it a dependable tool in clinical settings.