Accurate Ovulation (LH) Test Use By Fiatest GO Fluorescence
Immunoassay Analyzer In Serum / Plasma
The LH Test Cassette is intended for in vitro quantitative
determination luteinizing hormone (LH) in Whole Blood/Serum/Plasma
as an aid in the detection of ovulation.The test result is
calculated by Fluorescence Immunoassay Analyzer.
A rapid test for measuring Ovulation in whole blood
/serum /plasma with the use of Fiatest TM Go fluorescence Immunoassay Analyzer. For professional in vitro diagnostic use only.
| Product Name: | Accurate Ovulation (LH) Test Use By Fiatest GO Fluorescence
Immunoassay Analyzer In Serum / Plasma |
| Format: | Cassette |
| Certificate: | CE |
| Pack: | 10T/25T |
| Shelf Life: | 2 Years |
| Detection Range: | 20~300 MIU/mL |
| Principle: | Fluorescence Immunoassay |
| Specimen: | WB/S/P |
| Reading Time: | 15 Minutes |
| Storage Temperature: | 4-30℃ |
| Cut-Off: | 40mIU/mL |
| Linearity Range: | 20~300 MIU/mL, R≥0.990 |
Application And Description:
Ovulation is the release of an egg from the ovary. The egg then
passes into the fallopian tube where it is ready to be fertilized.
In order for pregnancy to occur, the egg must be fertilized by
sperm within 24 hours after its release. Immediately prior to
ovulation, the body produces a large amount of luteinizing hormone
(LH) which triggers the release of a ripened egg from the ovary.
This “LH surge” usually takes place in the middle of the menstrual
cycle.1
The LH Test Cassette (Whole Blood /Serum/Plasma) is a complete
system to help predict the time of ovulation, and peak fertility.
It is during this fertile time that pregnancy is most likely to
occur.
The LH Test Cassette (Whole Blood /Serum/Plasma) detects the LH
surge in Whole Blood /Serum/Plasma, signaling that ovulation is
likely to occur in the next 24-36 hours. The test utilizes a
combination of antibodies including a monoclonal LH antibody to
selectively detect elevated levels of LH.
Important: The LH surge and ovulation may not occur in all
menstrual cycles.The LH Test cassette is a rapid test that
quantitatively detects the LH level in Whole Blood /Serum/Plasma
specimen. The test utilizes a combination of antibodies including a
monoclonal anti-LH antibody to selectively detect elevated levels
of LH.The minimum detection level is 20mIU/mL.
How to use?
Refer to FIATESTTM Fluorescence Immunoassay Analyzer Operation
Manual for the complete instructions on use of the Test. The test
should be conducted in room temperature.
Allow the test, specimen, buffer and/or controls to reach room
temperature (15-30°C) prior to testing.
1. Turn on the Analyzer power. Then according to the need, select
“Standard Test” or “Quick Test” mode.
2. Take out the ID card and insert it into the Analyzer ID Card
Slot.
3. Squeeze 75μL Whole Blood /Serum/Plasma into the buffer tube by
pipette; mix the specimen and the buffer well.
4. Add diluted specimen with a Pipette: Pipette 75μL diluted
specimen into the sample well of the test cassette. Start the timer
at the same time.
5. There are two test modes for Fiatest TM Go Fluorescence Immunoassay Analyzer, Standard Test mode and
Quick Test mode. Please refer to the user manual of Fiatest TM Go Fluorescence Immunoassay Analyzer for details.
“Quick Test” mode: After 15 minutes of adding sample, Insert the
test cassette into the Analyzer, click “QUICK TEST”, fill the test
information and click "NEW TEST" immediately.
The Analyzer will automatically give the test result after a few
seconds.
“Standard Test” mode: Insert the test cassette into the Analyzer
immediately after adding specimen, click “STANDARD TEST”, fill the
test information and click "NEW TEST" at the same time, The
Analyzer will automatically countdown 15 minutes. After the
countdown, the Analyzer will give the result at once.
| Catalogue Number | Item Name | Sample | Test Range | KIT size |
| FI-FLH-402 | LH Ovulation Test Cassette | WB/S/P | 1~75 mIU/mL | 10T/25T |
