definitions antibodies (also known as immunoglobulins abbreviated ig) are gamma globulin proteins...
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Definitions
Antibodies (also known as immunoglobulins abbreviated Ig) are gamma globulin proteins that are found in blood and are used by the immune system to identify and neutralize foreign objects, such as bacteria and viruses.
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Definitions- cont
AntigensA substance that when introduced into the
body stimulates the production of an antibody
ImmunoassayA laboratory technique that makes use of
the binding between an antigen and its homologous antibody in order to identify and quantify the specific antigen or antibody in a sample
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Definitions- cont AnalyteThe sample being analyzed and in
immunoasssays the analyte is either Antibody or Antigen
Avidity: The combined strength of multiple bond interactions with an antigen.
Affinity : The Strength of Interaction between a molcol of antibady and an epitope.
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Antigen
Is present naturally in the body like hormones
Is manufactured in special disease status for example human chorionic gonadotrophin hormone (HCG) which is normally produced by cells of the placenta in pregnancy is found in the body in some types of cancer
Is not present in the body in normal condition like drugs
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Introduction
The Antibody: An immunoglobulin, a specialized immune protein, produced because of the introduction of an antigen into the body, and which possesses the remarkable ability to combine with the very antigen that triggered its production (specific affinity)
The antibody recognises and bind to the antigenic determinant region of the antigen
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Labeled Immunoassays
Some antigen/antibody reactions not
detected by precipitation or
agglutination.
Looking for very small amounts.
Measured indirectly using a labeled
reactant.
Referred to as receptor-ligand assays
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Labels
Used to detect reaction which has
occurred.
Most common are: Radioactive Enzymes Fluorescent Chemiluminescent
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Enzyme Immunoassay Enzymes occur naturally and
catalyze biochemical reactions.
Enzymes are Cheap Readily available Have a long shelf life Easily adaptable to automation. Automation relatively inexpensive.
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Enzyme Immunoassay
Enzymes used include: Horseradish peroxidase Glucose-6-phosphate
dehydrogenase Alkaline phosphatase Β-D-galactosidase
Horseradish peroxidase and alkaline phosphatase are the most popular.
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ELISA technique
Is a biochemical technique used mainly in immunology to detect the presence of an antibody or an antigen in a sample.
The technique is divided into:
1- Competitive ELISA 2- Sandwich ELISA
3 -Indirect ELISA
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Competitive ELISA
The labelled antigen competes for
primary antibody binding sites with the
sample antigen (unlabeled). The more
antigen in the sample, the less labelled
antigen is retained in the well and the
weaker the signal.
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Sandwich ELISA
The ELISA plate is coated with Antibody to detect specific antigen
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Sandwich ELISA-Cont
Antibody bound to solid phase. If looking for antigen must have
multiple epitopes, bound antibody specific for one epitope, second labeled antibody added specific for a different epitope.
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Sandwich ELISA-Cont
Antigens detected can be Antibodies Hormones Proteins Tumor markers Microorganisms especially viruses
Enzyme label used to detect reaction
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Sandwich ELISA-Cont
1. Add patient sample with antigen.2. Antigen will bind to antibody bound to solid
phase.3. Add enzyme labeled antibody directed
against a different epitope on the antigen.4. Wash the plate, so that the unbound
antibody-enzyme conjugates are removed.
5. Add substrate, measure intensity of color.
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Sandwich ELISA
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Indirect ELISA
The protein antigen to be tested for is added to each well of ELISA plate, where it is given time to adhere to the plastic through charge interactions
A solution of non-reacting protein is added to block any plastic surface in the well that remains uncoated by the protein antigen
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Indirect ELISA-Cont
Then the serum is added, which contains a mixture of the serum antibodies, of unknown concentration, some of which may bind specifically to the test antigen that is coating the well.
Afterwards, a secondary antibody is added, which will bind to the antibody bound to the test antigen in the well. This secondary antibody often has an enzyme attached to it
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Indirect ELISA-Cont
A substrate for this enzyme is then
added. Often, this substrate changes
colour upon reaction with the
enzyme. The colour change shows
that secondary antibody has bound to
primary antibody, which strongly
implies that the donor has had an
immune reaction to the test antigen.
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Indirect ELISA-Cont
The higher the concentration of the
primary antibody that was present in
the serum, the stronger the colour
change. Often a spectrometer is
used to give quantitative values for
colour strength
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Indirect ELISA
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An example of an ELISA experiment Before starting the work read kit
instruction carefully
1- The 96 well plate is labeled carefully and the first wells are used to draw the standard curve
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An example of an ELISA experiment-Cont
The sample is added to plate in duplicate or triplicate and then the mean result is calculated
The quality control sample which is provided with the kit is treated as the test samples
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Standards or Calibrators
Substance of exact known concentration.
Usually run for each new lot number
Based on results create standard curve.
Standard curve used to “read” results or
built into machine to provide results.
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Results
After reading the results the standard curve is drawn were the concentration is blotted on the X-axis and the absorbance on the Y-axis
Concentration ng/ml
Absorption nm
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Results-cont
The standards concentrations is specified on the x-axis and the reading of each standard is specified on the y-axis and the standard curve is drawn
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Results-cont
This standard curve is used to determine the unknown concentration of each sample by finding the opposite concentration to the absorbance
Concentration ng/ml
Absorption nm
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Results-cont
The quality control sample concentration is determined from the standard curve and if the result is in the range given by the kit manufacturer the results could be accepted
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Competitive and Noncompetitive Immunoassays
The measurement of analyte in an immunoassay is achieved by using either
a competitive or a noncompetitive format.
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Competitive format unlabelled analyte (usually antigen) in the test sample is measured by its ability to compete with labeled antigen in the immunoassay.
The unlabeled antigen blocks the ability of the labeled antigen to bind because that binding site on the antibody is already occupied.
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Con’ted Thus, in a competitive immunoassay, less label
measured in the assay means more of the unlabeled (test sample) antigen is present. The amount of antigen in the test sample is inversely related to the amount of label measured in the competitive format (Figure 1-7).
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one step competitive format In the one step competitive format (see Figure 1-8), both the labeled antigen reagent (Ag*) and the unlabeled specimen (or test sample analyte) compete for a limited amount of antibody.
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two step competitive format In the two step competitive format, the antibody
concentration of the reaction solution is present in excess in comparison to the concentration of antigen. Antibody reagent is first incubated with specimen containing antigens of interest; then in the second step, labeled antigen is added. Remember that in the competitive format, less bound labeled antigen indicates more antigen present in the test sample. Two step competitive assay formats provide several fold improved assay sensitivity compared to one step assay formats.
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Noncompetitive (Sandwich) Method
Noncompetitive assay formats generally provide the highest level of assay sensitivity and specificity and are applied to the measurement of critical analytes such as cardiac and hepatitis markers. This format is referred to as a “sandwich” assay because analyte is bound (sandwiched) between two highly specific antibody reagents (Figure 1-10).
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Noncompetitive assay Noncompetitive assay formats can also utilize
either one step or two step methods, as with the competitive assay.
The two step assay format employs wash steps in which the sandwich binding complex is isolated and washed to remove excess unbound labeled reagent and any other interfering substances.
The two step noncompetitive format usually offers the highest specificity and sensitivity of all the assay formats discussed here.
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