The 17α-Hydroxyprogesterone Detection Kit (Homogeneous Enzyme Immunoassay) is a state-of-the-art diagnostic tool designed for the accurate measurement of 17α-hydroxyprogesterone in human serum. This hormone is a critical marker in the assessment of adrenal function and the diagnosis of congenital adrenal hyperplasia (CAH). The kit employs a homogeneous enzyme immunoassay method, ensuring high sensitivity and specificity. It is widely used in clinical laboratories and research settings due to its reliability and ease of use.

1. The kit features a homogeneous enzyme immunoassay method, which eliminates the need for separation steps, thereby simplifying the procedure and reducing the risk of errors. This method ensures high sensitivity and specificity, making it ideal for clinical diagnostics.
2. The composition of the kit includes two main reagents: Reagent 1 and Reagent 2. Reagent 1 contains Tris base, glucose-6-phosphate, NAD+, sodium chloride, magnesium chloride, rabbit anti-human 17α-hydroxyprogesterone polyclonal antibody, bovine serum albumin, and a preservative. Reagent 2 contains Tris base, sodium chloride, magnesium chloride, glucose-6-phosphate dehydrogenase-17α-hydroxyprogesterone conjugate, bovine serum albumin, and a preservative. These components work synergistically to ensure accurate detection of 17α-hydroxyprogesterone levels.
3. The primary use of this kit is for the quantitative in vitro determination of 17α-hydroxyprogesterone levels in human serum samples. It is particularly useful in the diagnosis and monitoring of congenital adrenal hyperplasia (CAH) and other adrenal disorders. The kit provides reliable and precise results, making it an essential tool in endocrinology and reproductive health.

The 17α-Hydroxyprogesterone Detection Kit, also known as the 17-OHP Kit, is a vital tool in clinical diagnostics. Its homogeneous enzyme immunoassay method ensures high accuracy and reliability, making it indispensable for assessing adrenal function and diagnosing conditions like congenital adrenal hyperplasia. The kit's composition and design reflect a commitment to precision and ease of use, solidifying its place in modern medical practice.

The 17α-Hydroxyprogesterone Detection Kit offers high sensitivity and specificity, making it an essential tool for clinical diagnostics. Its homogeneous enzyme immunoassay method simplifies the detection process, ensuring accurate and reliable results.

1. High Sensitivity: The kit is designed to detect low levels of 17α-hydroxyprogesterone with high precision, making it suitable for early diagnosis and monitoring of adrenal disorders.
2. Specificity: The use of specific antibodies and enzymes ensures that the kit accurately measures 17α-hydroxyprogesterone without cross-reactivity with other similar compounds.
3. Ease of Use: The homogeneous enzyme immunoassay method eliminates the need for separation steps, simplifying the procedure and reducing the risk of errors.
4. Reliability: The kit provides consistent and reproducible results, making it a trusted tool in clinical laboratories.
5. Wide Application: The kit is widely used in the diagnosis and monitoring of congenital adrenal hyperplasia (CAH) and other adrenal disorders, making it an essential tool in endocrinology.

The 17α-Hydroxyprogesterone Detection Kit stands out for its high sensitivity, specificity, and ease of use. Its reliable performance and wide application in clinical diagnostics make it an indispensable tool for healthcare professionals. The kit's design reflects a deep understanding of the needs of modern medical practice, ensuring that it meets the highest standards of accuracy and reliability.

The 17α-Hydroxyprogesterone Detection Kit is widely used in clinical settings for the diagnosis and monitoring of adrenal disorders, particularly congenital adrenal hyperplasia (CAH). Its accurate and reliable results make it an essential tool in endocrinology.

1. Diagnosis of CAH: The kit is primarily used for the early diagnosis of congenital adrenal hyperplasia, a genetic disorder affecting adrenal function.
2. Monitoring Treatment: It is also used to monitor the effectiveness of treatment in patients with CAH, ensuring that hormone levels are within the normal range.
3. Adrenal Function Assessment: The kit is used to assess adrenal function in patients with suspected adrenal disorders, providing critical information for diagnosis and treatment.
4. Research Applications: The kit is also used in research settings to study the role of 17α-hydroxyprogesterone in various physiological and pathological processes.
5. Screening Programs: The kit is employed in newborn screening programs to detect CAH early, allowing for timely intervention and management.

The 17α-Hydroxyprogesterone Detection Kit plays a crucial role in the diagnosis and management of adrenal disorders, particularly congenital adrenal hyperplasia. Its accurate and reliable results make it an essential tool in clinical practice, ensuring that patients receive timely and effective treatment. The kit's wide application in both clinical and research settings underscores its importance in modern medicine.

When purchasing the 17α-Hydroxyprogesterone Detection Kit, it is important to consider factors such as product specifications, types, budget, and intended use to ensure that the kit meets your specific needs.

1. Product Specifications: Ensure that the kit meets the required specifications for sensitivity, specificity, and accuracy. Check the composition and storage conditions to ensure compatibility with your laboratory setup.
2. Product Types: Consider the different types of kits available, such as those designed for specific applications or with additional features. Choose the one that best fits your clinical or research needs.
3. Budget: Evaluate the cost of the kit in relation to your budget. Consider the long-term benefits of investing in a high-quality kit that provides reliable and accurate results.
4. Intended Use: Determine the primary use of the kit, whether for clinical diagnostics, research, or screening programs. Ensure that the kit is suitable for your intended application.

Purchasing the 17α-Hydroxyprogesterone Detection Kit requires careful consideration of various factors, including product specifications, types, budget, and intended use. By taking these factors into account, you can ensure that the kit meets your specific needs and provides reliable and accurate results. The right choice will enhance your diagnostic capabilities and contribute to better patient outcomes.

When using the 17α-Hydroxyprogesterone Detection Kit, it is important to follow the recommended procedures and precautions to ensure accurate and reliable results.

1. Proper Storage: Store the kit at the recommended temperature to maintain the stability and effectiveness of the reagents. Avoid exposure to extreme temperatures or direct sunlight.
2. Handling: Handle the reagents with care to avoid contamination. Use sterile techniques and ensure that all equipment is clean and properly calibrated.
3. Sample Preparation: Follow the recommended procedures for sample preparation to ensure accurate results. Avoid hemolysis or contamination of the serum samples.
4. Calibration: Regularly calibrate the equipment used with the kit to ensure accurate measurements. Follow the manufacturer's guidelines for calibration and maintenance.
5. Disposal: Dispose of used reagents and samples according to local regulations and guidelines. Ensure proper disposal to avoid environmental contamination.

Using the 17α-Hydroxyprogesterone Detection Kit requires careful attention to storage, handling, sample preparation, calibration, and disposal. By following the recommended precautions, you can ensure accurate and reliable results, enhancing the effectiveness of your diagnostic procedures. Proper use of the kit not only improves patient outcomes but also contributes to the overall quality of your laboratory work.