vendredi 31 octobre 2014

Basic Knowledge On Thyroid ELISA Kits

By Jocelyn Davidson


Enzyme linked Immunosorbent Assay is a process in medical diagnostics where specific protein molecules are calibrated or if they are present in a given sample. This is mainly used in figuring out if there is any disease or innate conditions in a person to adhere adequate medication as soon as possible.

HIV tests are one of the many examples of ELISA. It detects antibodies which are connected to the virus that are inside the blood of the patient. As for thyroid glands, Thyroid ELISA kits are used in most laboratories for further studying the present protein molecules. With this, other various kits are existent depending on what use they are.

Finding out if you have any specific food allergy is also done using this test. It may be used for testing if a patient is using illegal drugs. Generally, it is a tool for plant pathology and quality control check for certain industries. The calibration or reading is through how vibrant the color is and its changes after each sample is tested.

Two types of ELISA tests are widely used in laboratories. The first one is indirect which detects the antibodies in a given sample. An example for indirect is HIV testing, where it detects the antibodies in the sample which are against the virus. The second one is called capture or sandwich. It detects the antigens and then capture them between two antibodies. A good sample for this would be on pregnancy tests which detects the hCG or the human chorionic gonadotropin.

Various ways of collecting fluid samples from patients are possible, but the two most common are urine and blood. Urine and blood are placed in a container, or most likely a test tube, then are sent out to the hospital laboratories or clinics for analysis and testing. Inside the laboratory, the testing would start if there is any present antigen or antibody.

As for human blood, it is made up of plasma, red cells, and white blood cells. What is needed for the tests are blood serum. It is plasma that is stripped off with the clotting behaviour through centrifuge which spins the samples in high speed to separate the blood in different parts. The cells would be on the bottom while the serum stays on top.

There are enzyme substrate combinations that can be used for detection. The one enzyme used the most is Horseradish Peroxidase. This cleaves or separates the substrate molecules Ortho Phenylenediamine Dihydrochloride, or OPD, and Tetramethylbenzidine, or TMB, from each other. The result would be a yellow color when these two are separated. Then a plate reader is used to measure the optical density.

In cases where the patient has revealed to have a disease or other conditions, the sample will have antibodies for that specific disease. The antibodies will then attach to these antigens that are the bonding agents in these ELISA tests. The samples would then be cleaned or washed away with a different solution so that the remaining in the sample would be the antigens or the antibodies that are clinging to the antigens.

To get results through color changes, enzyme solutions would be added to the samples to get either a positive or a negative result. But there is a certain possibility for the test results to give a false positive. A false positive is when a sample has no infection or whatever but still gives a positive result. Even so, ELISA tests are reliable and considered to be a standard in the immunology community.




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