enzyme-linked-immunosorbent serologic assay Antonyms
No Synonyms and anytonyms found
Meaning of enzyme-linked-immunosorbent serologic assay
enzyme-linked-immunosorbent serologic assay (n)
an assay that relies on an enzymatic conversion reaction and is used to detect the presence of specific substances (such as enzymes or viruses or antibodies or bacteria)
enzyme-linked-immunosorbent serologic assay Sentence Examples
- Enzyme-linked-immunosorbent serologic assay (ELISA) is a widely used laboratory technique to detect and quantify substances such as peptides, proteins, antibodies, and hormones.
- The ELISA procedure involves immobilizing an antigen on a solid support, then adding an antibody specific to the antigen.
- After washing away unbound antibodies, an enzyme-linked secondary antibody is added to bind to the primary antibody.
- Finally, a substrate is added to the mixture, which is converted by the enzyme to produce a colored product that can be measured.
- The intensity of the color is proportional to the amount of antigen present in the sample.
- ELISAs are used in a variety of applications, including research, diagnostics, and quality control.
- One common application of ELISA is to detect and quantify antibodies in a patient's serum.
- ELISAs can also be used to detect and quantify antigens in a sample.
- For example, an ELISA can be used to detect the presence of a virus in a patient's blood.
- ELISAs are a powerful tool for detecting and quantifying substances in a sample.
FAQs About the word enzyme-linked-immunosorbent serologic assay
an assay that relies on an enzymatic conversion reaction and is used to detect the presence of specific substances (such as enzymes or viruses or antibodies or
No synonyms found.
No antonyms found.
Enzyme-linked-immunosorbent serologic assay (ELISA) is a widely used laboratory technique to detect and quantify substances such as peptides, proteins, antibodies, and hormones.
The ELISA procedure involves immobilizing an antigen on a solid support, then adding an antibody specific to the antigen.
After washing away unbound antibodies, an enzyme-linked secondary antibody is added to bind to the primary antibody.
Finally, a substrate is added to the mixture, which is converted by the enzyme to produce a colored product that can be measured.
