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ELISA - Wikipedia
The enzyme-linked immunosorbent assay (ELISA) (/ ɪ ˈ l aɪ z ə /, / ˌ iː ˈ l aɪ z ə /) is a commonly used analytical biochemistry assay, first described by Eva Engvall and Peter Perlmann in 1971. [1]

ELISA: What It Is, Purpose, Procedure & Results - Cleveland Clinic
What is ELISA? ELISA is a common laboratory testing technique that detects and counts certain antibodies, antigens, proteins and hormones in bodily fluid samples. This includes blood, plasma, pee, saliva (spit) and cerebrospinal fluid (CSF). “ELISA” stands for “enzyme-linked immunosorbent assay.” Another name for it is an EIA test.

Overview of ELISA | Thermo Fisher Scientific - US
Learn about the different methods for performing an ELISA assay for protein quantitation, including assay design strategies and reagents.

Enzyme Linked Immunosorbent Assay - StatPearls - NCBI Bookshelf
Enzyme-linked immunosorbent assay (ELISA) is a heterogeneous EIA technique used in clinical analyses.[1] In this type of assay, one of the reaction components is nonspecifically adsorbed or covalently bound to the surface of a solid phase, such as a microtiter well, a magnetic particle, or a plastic bead.

What is ELISA? - Types, Procedure, Principle, and Applications - BYJU'S
ELISA is the basic assay technique, known as enzyme-linked immunosorbent assay (also referred to as EIA: Enzyme Immunoassay) that is carried out to detect and measure antibodies, hormones, peptides and proteins in the blood. Antibodies are blood proteins produced in response to a specific antigen.

ELISA : Principle, Procedure, Types, Applications and Animation
An enzyme conjugated with an antibody reacts with a colorless substrate to generate a colored reaction product. A number of enzymes have been employed for ELISA, including alkaline phosphatase, horseradish peroxidase, and B-galactosidase. Principle of ELISA. ELISA is a plate-based assay technique.

Enzyme-linked immunosorbent assay (ELISA) - Microbe Notes
Enzyme-Linked Immunosorbent Assay (ELISA) is a modern molecular technique for the detection of antigen-antibody interaction with the help of an enzyme. It is one of the sensitive enzyme immunoassay techniques for the detection of the presence of antigen or antibody and quantification as well in the case of clinical diagnosis of many diseases.

Enzyme-linked immunosorbent assay (ELISA) | British Society for Immunology
The enzyme-linked immunosorbent assay (ELISA) is an immunological assay commonly used to measure antibodies, antigens, proteins and glycoproteins in biological samples. Some examples include: diagnosis of HIV infection, pregnancy tests, and measurement of cytokines or soluble receptors in cell supernatant or serum.

ELISA- Principle, Types, Uses, Advantages and Disadvantages
ELISA is based on antigen-antibody reactions, it represents the chemical interaction of antigen and antibody produced by immune cells i.e., leukocytes; ELISA allows selective quantitative/ qualitative analysis of antigens which also includes protein, peptides, hormones, nucleic acids, metabolites.

ELISA- Definition, Principle, Procedure, Types, Steps, Applications
ELISA (enzyme-linked immunosorbent assay) is a technique for detecting the presence of antigens in biological materials. An ELISA, like other types of immunoassays, uses antibodies to detect a target antigen via highly specific antibody-antigen interactions.

 

 

 

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