ELISA is short for enzyme linked immunosorbent assay. This is a diagnostic medical test to see if there is any present antibody or antigen in the body of a person. Its purpose is for calibrating the immunity of a person in terms of diseases and viruses. It identifies the protein concentration in the bodily fluids of a person.
One of these examples is for HIV, where it finds antibodies related to the virus inside the blood. Another would be for the thyroid glands, and the common equipment that are used in laboratories are Thyroid ELISA kits. These kits are used for studying the thyroid glands, as well as other types of kits are used for other body parts.
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.
A centrifuge is used to make a blood serum which is used during the tests. The centrifuge would separate the compositions of the blood which are the cells and the plasma. A blood serum is the actual sample used in tests, and the clotting feature is actually taken out already.
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.
One of these examples is for HIV, where it finds antibodies related to the virus inside the blood. Another would be for the thyroid glands, and the common equipment that are used in laboratories are Thyroid ELISA kits. These kits are used for studying the thyroid glands, as well as other types of kits are used for other body parts.
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.
A centrifuge is used to make a blood serum which is used during the tests. The centrifuge would separate the compositions of the blood which are the cells and the plasma. A blood serum is the actual sample used in tests, and the clotting feature is actually taken out already.
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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