Payment & Shipping Terms:
|Specimen:||Swab||Testing Time:||5-15 Minutes|
|Shelf Life:||24 Months||Application:||Rubella|
Rubella Rapid Diagnostic Cassette to detect IgM antibody of Rubella in human blood, easiy and quick
Rubella Rapid Diagnostic test
The Rubella Rapid Test Device is a panel of rapid qualitative lateral flow test designed for the quantitive detection of IgM antibodies to Rubella in human serum/plasma samples.
The Rubella Rapid Test Cassette (Serum/Plasma) is a qualitative, lateral flow immunoassay for the detection of antibodies to Rubella in serum or plasma specimens. In this test, mouse anti-human IgG and mouse anti-human IgM are coated in the test line regions of the test. During testing, the serum or plasma specimen reacts with Rubella antigen coated particles in the test strip. The mixture then migrates forward on the membrane by capillary action and reacts with the mouse anti-human IgG or mouse anti-human IgM on the membrane in the test line region. The presence of a colored line in the test line region indicates a positive result for Rubella infection, while its absence indicates a negative result for that infection.
To serve as a procedural control, a colored line will always appear in the control line region of the strip indicating that proper volume of specimen has been added and membrane wicking has occurred.
1. Bring the pouched test device to room temperature(15-30℃) prior to testing. Do not open the pouch until ready to begin testing.
2. Remove the device from the sealed pouch and lay it on a flat and dry surface.
3. Using the provided pipette, add one drop of fresh specimen to the sample well.
4. Hold the buffer bottle vertically and add 1 drop to the sample well. /If using a pipette, change a new one to avoid cross-contamination. Draw and transfer 2-3 drops of buffer to the sample well.
5. Read the result between 15-20minutes. Do not read results after 20 minutes.
INTERPRETATION OF RESULTS
POSITIVE:* Two lines appear. One colored line should be in the control line region (C) and another apparent colored line should be in the test line region (T).
*NOTE: The intensity of the color in the test line region (T) will vary depending on the concentration of TP antibodies present in the specimen. Therefore, any shade of color in the test line region (T) should be considered positive.
NEGATIVE: One colored line appears in the control line region (C). No line appears in the test line region (T).
INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
A clinical evaluation was conducted comparing the results obtained using the Rubella Rapid Test Cassette to Rubella ELISA Testing.
Table: Clinical Study from
|Rapid Test Cassette||Positive||68||2||70|
|Relative Sensitivity: 97.1% (95%CI*: 90.1%-99.7%)||*Confidence Interval|
|Relative Specificity: 99.3% (95%CI*: 97.6%-99.9%)|
|Accuracy: 98.9% (95%CI*: 97.3%-99.7%)|
|ORIENT NEW LIFE MEDICAL CO., LTD.|
|Email:||Jerry @ newlifebiotest .com|
Contact Person: Jerry Meng