ELISA elaborate as Enzyme Immuno Assays/Enzyme Linked Immuno Sorbent Assay.
These two terms go synonymous with each other with little modification in the test system.
ELISAs finds an enormous utility in the field of immuno diagnostics and are immuno chemical methods for the determination of anlytes such as
v Proteins/Peptides
v Bacterial and viral antigens and their specific antibodies,
v Hormones
The crucial element of detection is an antigen and antibody interaction (immune complex).
The immune complexes are detected and measured by means of an enzyme label that is conjugated to appropriate biomolecules.
EIA/ELISA
The enzyme activity is detected by means of a specific substrate
In the subsequent steps Substrate yields a colour
The intensity of colour can be measured in photometer.
The intensity of colour is proportional to the analyte concentration in serum.
ELISA makes use of Microtitre plates
Ø which are made up of polystyrene
Ø On to which biomolecules are passively or covalently absorbed.
ELISA as screening test……..
ELISAs are preferred screening tests in the detection and diagnosis of most of the infectious diseases because of their
ü Speed
ü Sensitivity
ü Specificity
ü Selectivity and
ü Simplicity to perform.
ELISAs do not involve any hazardous radioactive material and are safe to perform.
Enzyme labels used in ELISA
Compounds used for labeling biomolecules: