The 17α-Hydroxyprogesterone Assay Kit (Time-Resolved Immunofluorescence Method) is a state-of-the-art diagnostic tool designed for the precise measurement of 17α-OHP in neonatal blood samples. This kit employs advanced time-resolved immunofluorescence technology, ensuring high sensitivity and specificity. It is an essential tool for early detection of congenital adrenal hyperplasia (CAH) and other hormonal disorders.

1. The kit features high sensitivity and specificity, making it ideal for detecting low concentrations of 17α-OHP in neonatal blood samples. Its advanced immunofluorescence technology ensures accurate results even in complex biological matrices.
2. The kit includes a comprehensive set of components such as calibrators, tracers, primary antibodies, and quality controls. These components are meticulously designed to work together, ensuring reliable and reproducible results.
3. The primary use of this kit is in neonatal screening programs to detect congenital adrenal hyperplasia (CAH). It is also used in research settings to study hormonal imbalances and their effects on neonatal health.

The 17α-Hydroxyprogesterone Assay Kit is a vital tool in neonatal screening, offering unparalleled accuracy and reliability. Its advanced technology and comprehensive components make it a preferred choice for clinicians and researchers alike.

The 17α-Hydroxyprogesterone Assay Kit offers high sensitivity, specificity, and reliability in measuring 17α-OHP levels. Its advanced immunofluorescence technology ensures accurate results, making it a trusted tool in neonatal screening.

1. High Sensitivity: The kit can detect very low concentrations of 17α-OHP, making it ideal for neonatal screening.
2. Specificity: The kit's antibodies are highly specific to 17α-OHP, reducing the risk of cross-reactivity with other hormones.
3. Reliability: The inclusion of quality controls and calibrators ensures consistent and reproducible results.
4. Ease of Use: The kit is designed for straightforward operation, with clear instructions and user-friendly components.
5. Advanced Technology: The use of time-resolved immunofluorescence technology enhances the accuracy and precision of the assay.

The 17α-Hydroxyprogesterone Assay Kit stands out for its high sensitivity, specificity, and reliability. Its advanced technology and user-friendly design make it an indispensable tool in neonatal screening and research.

The 17α-Hydroxyprogesterone Assay Kit is primarily used in neonatal screening for congenital adrenal hyperplasia (CAH). It is also employed in research to study hormonal imbalances and their impact on neonatal health.

1. Neonatal Screening: The kit is widely used in neonatal screening programs to detect congenital adrenal hyperplasia (CAH) early.
2. Research: It is used in research settings to study the effects of hormonal imbalances on neonatal development.
3. Clinical Diagnostics: The kit aids in the diagnosis of various hormonal disorders in neonates.
4. Monitoring: It is used to monitor the effectiveness of treatments for hormonal disorders.
5. Public Health: The kit plays a crucial role in public health initiatives aimed at reducing the incidence of CAH and related disorders.

The 17α-Hydroxyprogesterone Assay Kit is a cornerstone in neonatal screening and research. Its applications extend from clinical diagnostics to public health, making it a versatile and essential tool.

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

1. Product Specifications: Ensure the kit includes all necessary components and meets the required sensitivity and specificity standards.
2. Product Types: Choose between different kit formats based on your laboratory's needs and throughput.
3. Budget: Consider the cost of the kit and any additional expenses such as shipping and storage.
4. Intended Use: Ensure the kit is suitable for your specific application, whether for neonatal screening, research, or clinical diagnostics.

Purchasing the 17α-Hydroxyprogesterone Assay Kit requires careful consideration of specifications, types, budget, and intended use. Making an informed choice ensures the kit meets your needs and delivers reliable results.

Proper handling and storage of the 17α-Hydroxyprogesterone Assay Kit are crucial to ensure accurate results and prolong the kit's shelf life.

1. Storage: Store the kit components at the recommended temperatures to maintain their stability and effectiveness.
2. Handling: Follow the manufacturer's instructions for handling the kit components to avoid contamination and ensure accurate results.
3. Expiration: Always check the expiration date before use and do not use expired components.
4. Disposal: Dispose of used components according to local regulations and guidelines.
5. Training: Ensure that all personnel using the kit are properly trained in its operation and handling.

Proper storage, handling, and disposal of the 17α-Hydroxyprogesterone Assay Kit are essential for maintaining its effectiveness and ensuring accurate results. Training personnel and adhering to guidelines further enhance the kit's reliability.