quickly and easily CRP Rapid Diagnostic Test, diagnosis of
myocardial infarction (MI), gold colloidal method
|Product||Cat No||Specimen||Sensitivity||Format||Kit Size|
|CrP (C-reactive protein )||YC105C4||WB / S / P||See Insert||4mm Cassette||25T|
The CRP Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid
chromatographic immunoassay for the qualitative detection of human
CrP in whole blood, serum or plasma as an aid in the diagnosis of
myocardial infarction (MI). The cutoff of the test is 10 μg/ml.
C-reactive Protein (CrP) in patient’s sera has been found in
association with acute infections, necrotic conditions and a
variety of inflammatory disorders. There is a strong correlation
between serum levels of CrP and the onset of the inflammatory
process. Monitoring the levels of CrP in patient’s sera indicates
the effectiveness of treatment and the assessment of patient
recovery. It is used in particular to differentiate bacterial
infections from virus infections
The CrP Rapid Test Cassette (Whole Blood/Serum/Plasma) detects
C-reactive Protein through visual interpretation of color
development on the internal cassette. The sample now moves through
the test cassette from bottom to top. If the test sample contains
CrP, it attaches to the anti-CrP antibody which is conjugated with
a red gold colloidal for color marking. The more CrP is contained
in the sample, the more red lines become visible. A red line should
always appear in the control (C) line area. It serves as a
procedural control, confirming that sufficient specimen volume was
used and indicates an adequate membrane wicking and proper
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
3. Open the tube with the diluted sample .Transfer 3 drops of mixed
specimens to sample well. Start the timer.
4. Wait for the colored lines to appear. The result should be read
at 5 minutes. Do not interpret the results at 10 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.