CDIA™ Human Hepatitis A Virus IgG/IgM Test Kit - Creative Diagnostics

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CDIATM Human Hepatitis A Virus IgG/IgM Test Kit (DTS649)

Intended Use

CD HAV IgG/IgM Rapid Test is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to Hepatit A virus in human serum or plasma. This test provides only a preliminary test result. Therefore, isolation of virus, PCR and RT-PCR, more specific alternative diagnosis method must be used in order to obtain a confirmation of Hepatit is A virus infection.
  • Serum, plasma
  • Kit
  • HAV IgG/IgM : Sensitivity -97.6%HAV IgM : Sensitivity - 99.3%

Product Introduction

General Description
Hepatitis A is caused by infection with the hepatitis A virus (HAV), a nonenveloped RNA agent that is classified as a picornavirus. Hepatitis A is an acute infectious disease of the liver. It can be serious for older people and people who already have liver disease. Death is possible, although very rare. The incubation period of hepatitis A is 15~50 days, with an average of 28 days. The illness caused by HAV infection typically has an abrupt onset of signs and symptoms that include fever, malaise, anorexia, nausea, and abdominal discomfort, several days later by dark urine and jaundice. Hepatitis A is spread through feces. People can get infected through close contact with an infected person and eating contaminated food or drinking contaminated water.
Principle Of The Test
CD HAV IgG/IgM Rapid Test is designed to simultaneously detect and differentiate IgG and IgM antibodies to Hepatitis A virus in human serum or plasma. CD HAV IgG/IgM test device has 3 pre-coated lines, “G” (HAV IgG Test Line), “M” (HAV IgM Test Line) and “C” (Control Line) on the surface of the membrane. All three lines in result window are not visible before applying any samples. The “Control Line” is used for procedural control. Control line should always appear if the test procedure is performed properly and the test reagents of control line are working. A purple “G” and “M” lines will be visible in the result window if there are enough IgG and/or IgM antibodies to Hepatitis A virus in the sample. If IgG and/or IgM antibodies to Hepatitis A virus are not present in the sample, there is no color appearance in “G” and/or “M”.

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