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Elisa ppt
The enzyme-linked immunosorbent assay (ELISA) is a common laboratory technique used to measure the concentration of an analyte like antibodies or antigens in solution. It works by using the principle of antigen-antibody binding and an enzyme-linked secondary antibody or antigen to detect the presence of an analyte. There are several types of ELISA including direct, indirect, sandwich, and competitive based on the procedure and detection method used. ELISA is a sensitive and specific technique with advantages like using inexpensive and stable reagents, but it also has limitations like possible false positives and negatives.
Elisa ppt
- 1. ELISA By: Dr. Saba Ahmed M.Phil.Pharmacology UNIVERSITY OF SARGODHA
- 2. Definition: • The enzyme-linkedimmunosorbent assay (ELISA) is a common laboratory technique which is used to measure the concentration of an analyte (usually antibodies or antigens) in solution.
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- 6. Basic Terms: • SolidPhase: Usually a microtiter plate well, having 8 12 well format.
- 7. Basic Terms: • Adsorption: Theprocess of adding an antigen/antibody, diluted in buffer, so it attaches to the solid phase on incubation. • Washing: The simple flooding & emptying of wells with a buffered solution to separate bound from un-bound reagents in ELISA.
- 8. Basic Terms: • Antigen: Anymolecule that elicits the production of antibodies when introduced into body. • Antibodies: Proteins produced in response to antigenic stimuli. • Enzyme conjugate: An enzyme that is attached irreversibly to an antibody. e.g: Horse-redish peroxidase (HRPO).
- 9. Basic Terms: • Chromogen: Achemical alters color as a result of an enzyme interaction with substrate (color reaction used as signal) e.g Trimethyl benzidine (TMB). • Stopping: The process of stopping the action of an enzyme on a substrate. • Reading: Spectrophotometric measurement of color developed in ELISA.
- 10. Principle of ELISA: Basedon Basic Immunology Response Lock and Key Concept: 1) Antigen (key) 2) Antibody (lock): –Key fits into the lock Enzyme conjugate substrates • Bound to a secondary antibody that binds with the antibody-antigen complex.
- 11. Equipments: 1) Microwell Plate: Flatbottom polystyrene plate, contains 8 x 12 wells holding 350 μL each.
- 12. Equipments: 2) Multipipette : An8-channel 100 μL pipette is a good help for even small-scale work.
- 13. Equipments: 3) Washing Device: •manually operated washing devices. • may be of use particularly when there is a risk that the samples tested in ELISA contain infectious material, so must be collected for subsequent disinfection.
- 14. Equipments: 4) Microplate washer: •These are very efficient with unusually low carry-over contamination.
- 15. Reagents Used: Reagent Composition CoatingBuffer 0.01 M Phosphate Buffer + 0.15 M NaCl (PBS) Diluting/Washing Buffer 0.01 M Phosphate Buffer + 0.50 M NaCl + 0.1% Tween 20 Blocking Buffer Bovine Serum Albumin (BSA) Enzyme Horse-redish peroxidase (HRPO) Chromogenic Substrate Trimethyl benzidine (TMB) Stop Solution 0.5 M H₂SO₄
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- 18. Types of ELISA: •On the Basis of Detection: 1) Colorimetric ELISA: Assay to Determine the Antibody Concentration.
- 19. Types of ELISA: 2)Chemiluminescent ELISA: Assay for the Quantitation of an Antigen in a Biological Sample.
- 20. Types of ELISA: 3)Competitive Fluorescence ELISA:
- 21. Types of ELISA: (onthe basis of procedure) Types Non- Competitive Direct Indirect SandwichCompetitive Multiple & Portable
- 22. Non-Competitive: 1) Direct ELISA: •It uses a primary labeled anti-body that react directly with the antigen. • It can be performed with the antigen that is directly immobilized on assay plate. • Not widely used but common for immuno-histochemical staining of cells & tissues.
- 23. Non-Competitive: 2) Indirect ELISA: •It utilizes a primary un-labeled antibody in conjunction with a labeled secondary antibody. • Secondary antibody has specificity for primary antibody.
- 25. Non-Competitive: 3) Sandwich ELISA: •Antigens like Tumor markers, hormones, serum proteins may be determined. • Antigens in the sample bind with the capture antibody & become immobilized. • The antibody of the enzyme conjugate bind with the immobilized antigen to form a sandwich of Ab-Ag-Ab/ enzyme bound to microwell.
- 27. Competitive: • Antibody coatedmicrowell. • Serum antigen & labeled antigen added together .... Competition • Ab-Ag enzyme complex bound is inversely related to the conc. of antigen present in sample. • Increased serum antigen results in reduced binding of Ag- enzyme conjugate with the antibody producing less enzyme activity & (yellow) color formation. • Used to determine small molecules like T₃ , T₄ & Progesterone.
- 31. Modified ELISA: • Enzymeinterfere with Ag-Ab interaction. • Second antibody is often labeled with a very small molecular substance, biotin (MW=244.31), and a specific binding protein for biotin, avidin is conjugated with enzyme such as HRP.
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- 33. Reading: • Measure theabsorbance at 450nm with the help of ELISA reader. • Calculate the absorbance for each sample and reference. • Ascent software for the calculation of results can be used.
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- 40. Precautions: 1) Use ofExchange type pipette: (always use new tip)
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- 44. Precautions: 4) Plate cover: •During incubation, well plate should be covered using the plate cover • Plate cover is effective only under suitable conditions i.e room temp. humidity > 50%, air steam <0.2 m/sec.
- 45. Precautions: 5) Coating ofwells: • Coating of wells should be proper with the addition of Blocking solution. • Improper coating False positive results
- 46. Advantages of ELISA: •Reagents are relatively cheap & ‘ve long shelf life. • It is highly specific & sensitive (<1pg/ml). • No radiation hazards occur during labeling or disposal of waste. • Easy to perform & quick procedures. • Equipment is widely available. • It can be used to a variety of infections. • It can be used on most type of biological samples like plasma, serum, urine, cell extracts.
- 47. Disadvantages of ELISA: •Measurement of enzyme activity can be more complex than the measurement of activity of some type of radioisotopes. • Enzyme activity may be affected by plasma constituents. • Kits are not cheap. • Very specific to particular antigen but won’t recognize other antigens. • False positive/ negative possible, especially with mutated/ altered antigen.
- 48. Limitations: • Results maynot be absolute. • Antibody must be available(poor producer, interference). • Concentration may be unclear. • False positive possible (Ab already present). • False negative possible.
- 50. References: • Gen. procedureof ELISA by DAKO A/S • Produktionsvej 42 • DK-2600 Glostrup • Denmark, www.dako.com • ENDOCRINE MANUAL FOR REPRODUCTIVE ASSESSMENT OF DOMESTIC AND NON-DOMESTIC SPECIES by Janine Brown, Ph.D , Sue Walker, M.S. • ELISA -A to Z .....from introduction to practice by Katsumi WAKABAYASHI, Ph.D , Prof. Emer. Gunma University. • www.wikipedia.com. • www.googleimages.com • www.slideshare.net • www.hhmi.org/biointeractive/immunology-virtual-lab. • www.ncbi.nlm.nih.gov/pubmed/25926946.
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