- Product name:Diagnostic Kit for Luteinizing Hormone
- Material:Plastic
- Usage:Home-testing
- MOQ:1000
- Accuracy:over 99%
- Feature:Convenient
- Power Source:Manual
- After-sale Service:Online Technical Support
- Material:Plastic
- Instrument classification:Class I
- Safety standard:MOL
- Place of Origin:CN
- Warranty:18 months
- Model Number:LH01
- Brand Name:Baysen
- Shelf Life:18 months
- Quality Certification:ISO
Product Description
Diagnostic Kit for Luteinizing Hormone
(fluorescence immunochromatographic assay)
For in vitro diagnostic use only
Please read this package insert carefully prior to use and strictly follow the instructions. Reliability of assay results cannot
be guaranteed if there are any deviations from the instructions in this package insert.
INTENDED USE
Diagnostic Kit for Luteinizing Hormone (fluorescence immunochromatographic assay) is a fluorescence immunochromatographic assay
for the quantitative detection of Luteinizing Hormone (LH) in human serum or plasma, which is mainly used in the evaluation of
pituitary endocrine function.All positive sample must be confirmed by other methodologies. This test is intended for healthcare
professional use only.
SUMMARY
Luteinizing hormone (LH) is a glycoprotein with a molecular weight of about 30,000 Dalton, which is produced by the anterior
pituitary. The concentration of LH is closely related to ovulation of ovaries, and the peak of LH is predicted to be 24 to 36
hours of ovulation. Therefore, the peak value of LH can be monitored during the menstrual cycle to determine the optimal
conception time. Abnormal endocrine function in the pituitary gland can cause LH secretion irregularity.The concentration of LH
can be used to evaluate pituitary endocrine function. The Diagnostic Kit is based on immunochromatography and can give a result
within 15 minutes.
PRINCIPLE OF THE PROCEDURE
The membrane of the test device is coated with anti LH antibody on the test region and goat anti rabbit IgG antibody on the
control region. Lable pad are coated by fluorescence labeled anti LH antibody and rabbit IgG in advance. When testing positive
sample, the LH antigen in sample combine with fluorescence labeled anti LH antibody, and form immune mixture. Under the action of
the immunochromatography, the complex flow in the direction of absorbent paper, when complex passed the test region, it combined
with anti LH coating antibody, forms new complex. LH level is positively correlated with fluorescence signal, and the
concentration of LH in sample can be detected by fluorescence immunoassay assay.
(fluorescence immunochromatographic assay)
For in vitro diagnostic use only
Please read this package insert carefully prior to use and strictly follow the instructions. Reliability of assay results cannot
be guaranteed if there are any deviations from the instructions in this package insert.
INTENDED USE
Diagnostic Kit for Luteinizing Hormone (fluorescence immunochromatographic assay) is a fluorescence immunochromatographic assay
for the quantitative detection of Luteinizing Hormone (LH) in human serum or plasma, which is mainly used in the evaluation of
pituitary endocrine function.All positive sample must be confirmed by other methodologies. This test is intended for healthcare
professional use only.
SUMMARY
Luteinizing hormone (LH) is a glycoprotein with a molecular weight of about 30,000 Dalton, which is produced by the anterior
pituitary. The concentration of LH is closely related to ovulation of ovaries, and the peak of LH is predicted to be 24 to 36
hours of ovulation. Therefore, the peak value of LH can be monitored during the menstrual cycle to determine the optimal
conception time. Abnormal endocrine function in the pituitary gland can cause LH secretion irregularity.The concentration of LH
can be used to evaluate pituitary endocrine function. The Diagnostic Kit is based on immunochromatography and can give a result
within 15 minutes.
PRINCIPLE OF THE PROCEDURE
The membrane of the test device is coated with anti LH antibody on the test region and goat anti rabbit IgG antibody on the
control region. Lable pad are coated by fluorescence labeled anti LH antibody and rabbit IgG in advance. When testing positive
sample, the LH antigen in sample combine with fluorescence labeled anti LH antibody, and form immune mixture. Under the action of
the immunochromatography, the complex flow in the direction of absorbent paper, when complex passed the test region, it combined
with anti LH coating antibody, forms new complex. LH level is positively correlated with fluorescence signal, and the
concentration of LH in sample can be detected by fluorescence immunoassay assay.
ASSAY PROCEDURE
The test procedure of the instrument see the immunoanalyzer manual. The reagent test procedure is as follows
1. Lay aside all reagents and samples to room temperature.
2. Open the Portable Immune Analyzer(WIZ-A101), enter the account password login according to the operation method of the instrument, and enter the detection interface.
The test procedure of the instrument see the immunoanalyzer manual. The reagent test procedure is as follows
1. Lay aside all reagents and samples to room temperature.
2. Open the Portable Immune Analyzer(WIZ-A101), enter the account password login according to the operation method of the instrument, and enter the detection interface.
1. Scan the dentification code to confirm the test item.
2. Take out the test card from the foil bag.
3. Insert the test card into the card slot, scan the QR code, and determine the test item.
4. Add 40μL serum or plasma sample to sample diluent, and mix well..
5. Add 80μL sample solution to sample well of the card.
6. Click the"standard test"button, after 15 minutes, the instrument will automatically detect the test card, it can read the results from the display screen of the instrument, and record/print the test results.
7. Refer to the instruction of Portable Immune Analyzer(WIZ-A101).
2. Take out the test card from the foil bag.
3. Insert the test card into the card slot, scan the QR code, and determine the test item.
4. Add 40μL serum or plasma sample to sample diluent, and mix well..
5. Add 80μL sample solution to sample well of the card.
6. Click the"standard test"button, after 15 minutes, the instrument will automatically detect the test card, it can read the results from the display screen of the instrument, and record/print the test results.
7. Refer to the instruction of Portable Immune Analyzer(WIZ-A101).
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