LH Assay Kit

LH Assay Kit

UD-Bio manufactures the LH Assay Kit, which utilizes the immunochromatographic assay principle, for the detection of LH concentration in human serum or plasma. The kit employs the double antibody sandwich method and is designed to be used with the Immunofluorescence Analyzer. To initiate the...
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Product Introduction

UD-Bio manufactures the LH Assay Kit, which utilizes the immunochromatographic assay principle, for the detection of LH concentration in human serum or plasma. The kit employs the double antibody sandwich method and is designed to be used with the Immunofluorescence Analyzer.

To initiate the testing process, the specimen adding hole receives a dose of human serum or plasma. This results in the LH present in the specimens to come in contact with the fluorescently-labeled LH antibody that resides on the bonding pad. As a result of this interaction, a complex known as the LH-antibody complex is formed.

The LH test is designed to measure the levels of luteinizing hormone in your bloodstream. This hormone is critical for both male and female reproductive systems, playing an important role in the operation of the ovaries in women and testes in men. Sometimes referred to as lutropin or interstitial cell stimulating hormone, LH is synthesized in the pituitary gland, a small organ located behind the nose. Through measuring LH levels, healthcare providers can better understand the function of the reproductive organs and may be able to diagnose and treat related conditions more effectively.

The quantitative detection of LH concentration in human serum or plasma can be achieved using the LH Assay Kit. LH, also known as luteinizing hormone, is a glycoprotein hormone that is secreted by pituitary basophils. It can be found in human blood and urine. The main function of LH is to stimulate the release of mature ovarian oocytes. In coordination with female follicle-stimulating hormone (FSH), LH plays a crucial role in regulating the ovarian menstrual cycle, which ultimately leads to ovulation and the formation of the luteal phase.


INDEX OF CHARACTERISTICS

:LH±15.0%。,。,ChapGPT,。

2. The Lowest Detection Limit:1 mIU/mL.

3. Within-run Precision:CV≤15%.

4. Between-run Precision:CV≤15%.

The measuring range for this test is 1 to 200mIU/mL, and the correlation coefficient (R) value is greater than 0.99, indicating strong correlation between the measured values.

LH concentration should not exceed 1 mIU/mL for specificity purposes.

7. Packing: 20 tests/kit

 


TEST PROCEDURE

To prepare for the test, remove the card from the fridge and let it sit at room temperature until it reaches the appropriate temperature. This will ensure accurate results and a successful test.

(20~25℃).

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To ensure the accuracy and reliability of the identification (ID) chip and diagnostic kits, it is crucial to verify the consistency between the ID chip and the lot number. When inserting the ID chip, be cautious not to touch the insertion end. Avoiding contact with the insertion end helps maintain the integrity of the chip and ensures its effectiveness. Please rearrange this information to create a highly similar content while conveying the same message.

To start the testing process, you must first open the foil pouch by carefully tearing along the splice. Once the pouch is opened, place the test card on a flat operation table. It is important to note that the test card should be used within 1 hour, so be sure to start the testing process as soon as possible after opening the foil pouch. By following these instructions, you will be able to ensure accurate and reliable test results.

To prepare the samples, take 70 μL of serum or plasma and transfer it to a sample dilution tube. Make sure to mix the samples thoroughly before proceeding with the analysis.

To add the mixture samples or reference material to the test card, hold the pipette vertically and carefully dispense 70 μL without any air bubbles into the sample well. Ensure accuracy and precision when conducting this step.

After allowing it to sit at room temperature for 15 minutes, the next step is to insert it into the test card holder of the analyzer and initiate the testing process following the instructions in the analyzer manual. The result will be generated automatically within a few seconds.

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It is important to handle the test card used with caution, especially in regards to any potential biological hazards. It is recommended that proper protocols be followed to ensure the safety of those who come in contact with the test card.

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