Brucella/ Brucellosis Antibody Rapid Test Kit
(Whole Blood / Serum / Plasma / Milk)
Brucella Antibody Rapid Test Kit (whole blood / serumr/ plasma/milk) is a solid phase immunochromatographic assay for the rapid,qualitative and dfferentia ldetection of antibody to animal whole blood serum, or plasma. This test provide only a preliminary analytical result. A secondary analytical method must be used to obtain a confirmed result. Gas chromatography and mass spectrometry (GC/MS) are the preferred confirmatory methods.
Quantitative or qualitative detection of the titer level of Brucella Antibodies in samples using a double antigen sandwich method. During detection, the Brucella Antibodies in the sample binds to the colloidal gold-coated specific antigen fragment to form an antigen-antibody complex, which flows along the test paper to the other end of the NC membrane. When the complex flows to the T-zone on the membrane, the antigen immobilized on the membrane captures the complex and gradually agglutinates into a red visible T-line, while the unbound colloidal gold antibody flows through the T-zone and is captured by the secondary antibody in the C-zone and forms a visible red C-line.
||Brucella Antibody Rapid Test
STORAGE AND STABILITY
1. Store in a light-proof, dry environment (2-30℃).
2. DO NOT FREEZE or use beyond the expiration date.
3. The shelf life is 18 months.
Allow test cassete, specimen, and/ or controls to equilibrate to room temperature (15-30℃) prior to testing.
1.Remove the test cassette from the sealed foil pouch and use it as soon as possible.Best results will be obtained if the assay is performed within one hour.
2. Place the test device on a clean and level surface.
3.Add100ul (3 drops)sample into the sample well.
3.Wait for the colored line(s)to appear.The result should be read at between 10-15 mintues.it is invalid after 15 minutes.
READ RESULTS WITH NAKED EYES
The Test Line (T) is the same as or darker than the Control Line(C). It is negative.
The Test Line (T) is lighter than the Control Line(C),or there is no Test Line. It is positive.
INVALID:Reference Line Fails to appear
Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for an invalid result.
Review the procedure and repeat the test with a new test kit. Stop using the test kit immediately if the problem
is not solved and contact your local distributor.