Luteinizing hormone (LH) Rapid Test

Short Description:

Used For: to qualitatively detect luteinizing hormone (LH) in urine to help detect ovulation. 

Specimen:Urine

Certification:CE

MOQ:1000

Delivery time:2-5 days after Get payment

Packing:20 tests kits/Packing box

Shelf Life:24 Months

Payment:T/T, Western Union, Paypal

Assay Time: 10-15 Minutes


Product Detail

Product Tags

INTENDED USE

The Luteinizing hormone (LH) Rapid Test is a colloidal gold immunochromatographic technology developed to qualitatively detect luteinizing hormone (LH) in urine to help detect ovulation. 

MATERIALS

Materials Provided

· Luteinizing hormone (LH) Rapid Test

· Droppers

· Package insert

 

Materials Required but Not provided

 

· Specimen collection containers

· Timer


TEST PROCEDURE

Allow the test, reagents, specimen, and/or controls to reach room temperature (15-30°C) prior to testing.

  1. 1. Determine the day to begin testing. (See the above section:“WHEN TO STARTTESTING”).
  2. 2. Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it within one hour.
  3. 3. Place the test cassette on a clean and level surface. Hold the sample dropper vertically and transfer 3 drops of urine (approx.90μl) to the specimen well of the test cassette, and then start the timer. Avoid trapping air bubbles in the specimen well. See illustration below.
  4. 4. Wait for the red line(s) to appear. Read the result at 5 minutes. Do not interpret the result after 10 minutes.
  5. INTERPRETATION OF RESULTS

    POSITIVE: Two colored bands appear on the membrane. And the line in test line region (T) is the same as or darker than the one in the control line region (C). This indicates probable ovulation in 24-36 hours.One band appears in the control region (C) and another band appears in the test region (T).

    NEGATIVE: Two lines are visible, but the line in the test line region (T) is lighter than the one in the control line region (C), or if there is no line in the test line region (T). This indicates that no LH surge has been detected.

    INVALID: Control band fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.

    LIMITATIONS OF THE TEST

    1. 1. The Luteinizing hormone (LH) Rapid Testis for professional in vitro diagnostic use, and should only be used as a form of birth control.
    2. 2. The test results should not be affected by pain relievers, antibiotics and other commondrugs. Medication containing hCG or LH may affect the test and should not be taken while usingLuteinizing hormone (LH) Rapid TestCassette (Urine). In addition, the test will not work properly for subjects who are pregnant, in menopause, or taking birth control pills.
    3. 3. Keep out of the reach of children.


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