Pack Size:20 test/kit
Achieve accurate and rapid diagnosis of dengue infections with the SD Dengue IgG/IgM Ab Rapid Test. This advanced test kit enables the detection of both IgG and IgM antibodies associated with dengue fever. With its high sensitivity and specificity, this test delivers reliable results, aiding in early identification and effective management of dengue cases. Trust the SD Dengue IgG/IgM Ab Rapid Test for efficient screening and monitoring, allowing for timely intervention and improved patient outcomes. Enhance your diagnostic capabilities by ordering this essential test kit today and effectively combat dengue
INTENDED USE :
It is a rapid solid phase Immuno-chromatographic test for the qualitative differential detection of IgM and IgG antibodies to dengue virus in Human serum /Plasma. This test is for in vitro diagnostic use only and is intended as an aid in for presumptive diagnosis between primary and secondary dengue infection.
Salient Features :
SD card test is based on immunochromatographic test principle for the differential detection of Dengue IgM/IgG antibodies. Dengue IgM/IgG test device contains three lines; “C” (Control line), “M”(IgM test line) & “G”(IgG test line).IgM test line is coated with anti-human IgM and IgG test line is coated with anti-human IgG.When a sample is added to the device,IgG and IgM antibodies in the sample react with red particles coated with Dengue proteins. As this sample/particle mixture migrates along the length of the test, the anti-dengue IgG or IgM antibody particle complex is captured by the relevant IgG and /or IgM test bands located in the test device window causing a pale to dark red band to form at the IgG or IgM Region of the test device window. The intensity of the test bands in the device will vary depending upon the amount of antigen /antibody present in the sample. The appreance of any pink/ red colour in a specific test region should be considered as positive for that particular antigen and/or antibody type (IgG or IgM). A red procedural control line should always develop in the test device window to indicate that the test has been performed properly.
For professional in vitro diagnostic use only. Do not use after expiration date. Do not eat, drink or smoke in the area where the specimens or kits are handled. Handle all specimens as if they contain infectious agents. and follow the standard procedures for proper disposal of specimens. Humidity and temperature can adversely affect results.
Storage & Stability :
The kit can be stored at room temperature or refrigerated (2-30°C). The test is stable through the expiration date printed on the sealed pouch. The test cassette must remain in the sealed pouch until use. DO NOT FREEZE. Do not use beyond the expiration date.
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