Gastrointestinal disease test kit
IgMHelicobacter pyloriserum

gastrointestinal disease test kit
gastrointestinal disease test kit
gastrointestinal disease test kit
gastrointestinal disease test kit
gastrointestinal disease test kit
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Characteristics

Applications
for gastrointestinal diseases
Tested parameter
IgM
Micro-organism
Helicobacter pylori
Sample type
serum, plasma, whole blood
Format
cassette
Result display time

Min.: 10 min

Max.: 20 min

Sample volume

0.035 ml
(0.00118 US fl oz)

Description

Helicobacter pylori (H.pylori) IgG/ IgM Test Kit (Colloidal Gold Method) is used for the in vitro qualitative detection of Helicobacter pylori antibody IgG/IgA in human serum/plasma/whole blood samples. For people who have not been treated for Helicobacter pylori eradication, combined with clinical and other laboratory indicators, it is used for the auxiliary diagnosis of Helicobacter pylori infection.Antibody detection products cannot be used for the recent judgment of the evaluation of the eradication effect of Helicobacter pylori. 【SHELF LIFE AND STORAGE】 Store in a dry place at 2~30 ℃ away from light. 2.Transport at 2-37℃ for 20 days 3. After opening the inner packaging, the test card will become invalid due to moisture absorption, please use it within 1 hour. 4. The shelf life of the test kit is 12 months from date of manufacture. 【Test procedure】 Before opening the bag, please leave it at room temperature. Take the test device out of the sealed bag and use it as soon as possible. The best results will be obtained if the measurement is performed within one hour. 【INTERPRETATION OF ASSAY RESULT】 1.NEGATIVE RESULT: If only the C line develops, the test indicates that no detectable hepatitis C virus is present in the specimen. The result is negative or non-reactive. 2. POSITIVE RESULT: In addition to the presence of the C line, if the T line develops, the test indicates the presence of hepatitis C virus. The result is hepatitis C virus positive or reactive. 3. INVALID If the C line does not develop, the assay is invalid regardless of color development of the T line as indicated below. Repeat the assay with a new device.

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