The 17α-Hydroxyprogesterone Control is a critical tool for ensuring the accuracy and reliability of 17α-OH-P testing in clinical laboratories. It is formulated to mimic patient samples, providing a consistent benchmark for quality control.

1. The 17α-Hydroxyprogesterone Control is characterized by its stability and consistency, making it an ideal choice for routine quality control in clinical laboratories.
2. The control is composed of chemically synthesized 17α-hydroxyprogesterone, preserved in Proclin 300, and stored in T3/T4-free negative human serum, ensuring its suitability for a wide range of testing environments.
3. This control is specifically designed for use in 17α-OH-P testing, providing a reliable benchmark for quality control. It is not intended for use in neonatal testing.

The 17α-Hydroxyprogesterone Control, also known as 17α-OH-P Control, is a vital component in ensuring the accuracy of 17α-OH-P testing. Its stable formulation and specific application make it a trusted choice for clinical laboratories.

The 17α-Hydroxyprogesterone Control offers reliable quality control for 17α-OH-P testing, ensuring consistent and accurate results in clinical laboratories.

1. The control provides a stable and consistent benchmark for 17α-OH-P testing, ensuring the reliability of test results.
2. It is formulated with chemically synthesized 17α-hydroxyprogesterone, ensuring its accuracy and suitability for quality control purposes.
3. The control is preserved in Proclin 300 and stored in T3/T4-free negative human serum, making it suitable for a wide range of testing environments.
4. It is specifically designed for use in 17α-OH-P testing, providing a reliable benchmark for quality control in clinical laboratories.
5. The control is not suitable for neonatal testing, ensuring its specific application in adult testing environments.

The 17α-Hydroxyprogesterone Control is a reliable and consistent tool for quality control in 17α-OH-P testing. Its specific formulation and application make it a trusted choice for clinical laboratories.

The 17α-Hydroxyprogesterone Control is widely used in clinical laboratories for quality control in 17α-OH-P testing, ensuring accurate and reliable results.

1. The control is used in clinical laboratories to ensure the accuracy and reliability of 17α-OH-P testing, providing a consistent benchmark for quality control.
2. It is specifically designed for use in adult testing environments, ensuring its suitability for a wide range of clinical applications.
3. The control is not suitable for neonatal testing, ensuring its specific application in adult testing environments.
4. It is used to monitor the performance of 17α-OH-P testing systems, ensuring consistent and accurate results.
5. The control is a critical tool for ensuring the quality of 17α-OH-P testing in clinical laboratories, providing a reliable benchmark for quality control.

The 17α-Hydroxyprogesterone Control is a vital tool in clinical laboratories, ensuring the accuracy and reliability of 17α-OH-P testing. Its specific application and reliable performance make it a trusted choice for quality control.

The 17α-Hydroxyprogesterone Control is a critical tool for quality control in 17α-OH-P testing. This guide provides essential information for purchasing the control, including product parameters, types, budget considerations, and usage scenarios.

1. Product parameters: The control is formulated with chemically synthesized 17α-hydroxyprogesterone, preserved in Proclin 300, and stored in T3/T4-free negative human serum.
2. Product types: The control is available in liquid form, suitable for use in a wide range of testing environments.
3. Budget considerations: The cost of the control should be considered in relation to its stability, consistency, and specific application in 17α-OH-P testing.
4. Usage scenarios: The control is specifically designed for use in adult testing environments, ensuring its suitability for a wide range of clinical applications.

The 17α-Hydroxyprogesterone Control is a reliable and consistent tool for quality control in 17α-OH-P testing. Its specific formulation and application make it a trusted choice for clinical laboratories.

The 17α-Hydroxyprogesterone Control requires careful handling and storage to ensure its stability and reliability in quality control applications.

1. The control should be stored at the recommended temperature to maintain its stability and consistency.
2. It should be handled with care to avoid contamination, ensuring its suitability for quality control purposes.
3. The control should be used within its expiration date to ensure its reliability in quality control applications.
4. It should not be used for neonatal testing, ensuring its specific application in adult testing environments.
5. The control should be used in accordance with the manufacturer's instructions to ensure its accuracy and reliability in quality control applications.

The 17α-Hydroxyprogesterone Control requires careful handling and storage to ensure its stability and reliability in quality control applications. Its specific application and reliable performance make it a trusted choice for clinical laboratories.