£9.95 Inclusive of all Taxes
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The CEA Rapid Test Cassette utilizes a combination of anti-CEA antibody coated particles and anti-CEA antibodies to detect elevated levels of CEA in whole blood, serum or plasma. The minimum detection level is 5ng/ml.
Features and Benefits
These tests are designed solely to be used by medical professionals
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The CEA Rapid Test Cassette utilizes a combination of anti-CEA antibody coated particles and anti-CEA antibodies to detect elevated levels of CEA in whole blood, serum or plasma. The minimum detection level is 5ng/ml.
Carcinoembryonic Antigen (CEA) is a tumour-associated antigen characterized as an oncofetal glycoprotein.CEA is expressed in a variety of malignancies, particularly pulmonary or gastrointestinal tumours (e.g. colon cancer, liver cancer and lung cancer). CEA normally occurs in fetal gut tissue with detectable serum levels essentially disappearing after birth. Therefore, elevated levels of CEA can be of significant value in the diagnosis of primary carcinomas.
In addition to qualitative assessment, CEA testing plays an important role in the monitoring of cancer patients. Clinical evidence indicates that CEA levels can serve as predictive markers in both pre- and post-treatment cancer. Progressive elevation of CEA may signal tumour recurrence 3-36 months before clinical evidence of metastasis. Persistent elevation of circulating CEA following treatment is strongly indicative of occult metastatic and residual diseases and deficient therapeutic response.
The CEA Rapid Test Cassette (Whole Blood/Serum/Plasma) utilizes a combination of anti-CEA antibody coated particles and anti-CEA antibodies to detect elevated levels of CEA in whole blood, serum or plasma. The minimum detection level is 5ng/ml.
The CEA Rapid Test Cassette (Whole Blood/Serum/Plasma) is a qualitative membrane based immunoassay for the detection of CEA in whole blood, serum or plasma. The membrane is pre-coated with anti-CEA antibodies on the test line region. During testing, the specimen reacts with the particle coated with anti-CEA antibodies. The mixture migrates upward on the membrane chromatographically by capillary action to react with anti-CEA antibodies on the membrane and generate a coloured line. The presence of this coloured line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a coloured line will always appear in the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.
You will receive:-
This kit assumes you are a medical professional and already have a fingertip blood collection device (e.g. safety lancet).
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