| Principle | Fluorescence Immunoassay |
| Format | Cassette |
| Specimen | WB/S/P |
| Certificate | CE |
| Reading Time | 3 minutes |
| Pack | 10T/25T |
| Storage Temperature | 4-30℃ |
| Shelf Life |
2 Years |
Fast Reading Menopause Test Use By Citest GO fluorescence Immunoassay Analyzer In Human whole blood /serum /plasma
A test for measuring Menopause CRP in whole blood /serum /plasma with the use of Citest TM Go fluorescence Immunoassay Analyzer. For professional in vitro diagnostic use only.
Application:
CRP Test Cassette (WB/S/P) is based on Fluorescence Immunoassay for the quantitative determination of C-reactive protein (CRP) in serum, plasma or whole blood as an aid in the evaluation of infection, tissue injury and inflammatory disorders along with measurement of high sensitivity CRP (hs-CRP) for evaluation of acute coronary syndromes (ACS).
Description:
Menopause is the permanent cessation of menstruation but is usually not scientifically diagnosed until one full year after a woman’s menstrual periods have stopped. The period leading up to menopause, and the 12 months following, is known as perimenopause. Many women experience symptoms during this time including hot flashes, irregular menstrual cycles, sleep disorders, vaginal dryness, hair loss, anxiety and mood swings, short-term memory loss and fatigue.
The onset of perimenopause is caused by changes in the levels of hormones in the female body that regulate the menstrual cycle. As the body produces less and less estro/gen, it increases its production of FSH, which normally regulates the development of a female’s eggs.1-3.
Therefore, testing for FSH can help determine whether a woman is in the perimenopause stage. If a woman knows she is perimenopausal, she can take the appropriate steps to keep her body healthy and avoid the health risks associated with menopause, which include osteoporosis, increased blood pressure and cholesterol, and increased risk of heart disease.
The FSH Test cassette is a rapid test that quantitatively detects the FSH level in Whole Blood /Serum/Plasma specimen. The test utilizes a combination of antibodies including a monoclonal anti-FSH antibody to selectively detect elevated levels of FSH. The minimum detection level is 10mIU/mL.
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【PERFORMANCE CHARACTERISTICS】 1. Accuracy The test deviation is≤±15%. 2. Assay Range and Detection Limit Assay Range: 0.1 – 50 ng/mL Minimum Detection Limit (Analytical Sensitivity): 0.1 ng/mL 3. Linearity range 0.1~50 ng/ml , R≥0.990 4. Precision CV≤15% |
Fast Result (3 minutes) Simple Operation (Less Training Required) Objective (Results Read by Analyzer) Stringent Quality Control Insure High Accuracy User-friendly (Simple Plug & Play Operation) High Efficiency (Both STAT Testing and Batch Testing) |
How to use?
Refer to Citest TM Fluorescence Immunoassay Analyzer Operation Manual for the complete instructions on use of the Test. The test should be in room temperature.
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 port.
3. Serum or plasma: Pipette 5 μL serum or plasma into the buffer tube, mix the specimenand the buffer well.
Whole blood: Transfer 7.5 μL whole blood into the buffer tube with sampler provided or pipette; mix the specimen and the buffer well.
4. Add diluted specimen with a Pipette: Pipette 75 μL diluted specimen into the sample well of the cassette. Start the timer at the same time.
Add specimen with sampler provided: Discard the first 2 drops, then add 2 drops of dilutedspecimen into the sample well of the cassette. Start the timer at the same time.
5. There are two test modes for Citest TM Fluorescence Immunoassay Analyzer, Standard Test mode and Quick Test mode. Please refer to the user manual of Citest Fluorescence Immunoassay Analyzer for details.
“Quick test” mode: Insert the test cassette into the Analyzer at 3 minutes after sample application 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 sample application, click “STANDARD TEST”, fill the test information and click "NEW TEST" at the same time, the Analyzer will automatically counting down 3 minutes. After the countdown, the Analyzer will give the result at once.
INTERPRETATION OF RESULTS
Results read by Citest TM Fluorescence Immunoassay Analyzer.
The result of tests for C-reactive Protein is calculated by Citest TM Fluorescence Immunoassay
Analyzer and display the result on the screen. For additional information, please refer to the user
manual of Citest TM Fluorescence Immunoassay Analyze.
Linearity range of FluroLit TM CRP is 0.5-200 mg/L.
ORDER INFORMATION
| Catalogue Number | Item Name | Sample | Test Range | KIT size |
| FI-CRP-402 | CRP Test Cassette | WB/S/P | 0.5~200 mg/L | 10T/25T |
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