Cell recognition and the immune system Flashcards
Explain th euse of antibodies in the ELISA(Enzyme-linked Immunosorbent Assay) test to detect antigens?
- attach sample with potenial antigens to well
- add complementary monoclonal antibodies woth enzyme attached–> bind to antigens if present
- wash well–> remove unbound antibodies (to prevent false positive)
- Add substrate–> enzymes create products that cause a colour change (positive result)
Explain th euse of antibodies in the sandwich ELISA(Enzyme-linked Immunosorbent Assay) test to detect antigens?
- attach sample with potenial antigens to well
- Add sample with potential antigens,then wash well
- add complementary monoclonal antibodies with enzymes attached –>bind to antigens if present
- Wash well-Remove unbound antibodies to prevent false positives
- Add subsrate–> enzymes create products that cause a colour change (positive result)
Explain the use of antibodies in the ELISA test to detect antibodies
- attach sample with potenial antigens to well
- Add sample with potential antibodies ,wash well
- add complementary monoclonal antibodies with enzymes attached –> bind to antibodies if present
- Wash well–>remove unbound antibodies
- Add substrae-Enzymes create products that cause a colour change
Suggest the purpose of a control well in the ELISA test
Compare to test to show only enzymes cuase colour change
Compare to test to show all unbound antibodies have been washed away
Discuss some general ethical issues associated with th euse of vaccines and monoclonal antibodies
Pre clinical testing on/use of animals- potential stress/harm/mistreatment
-But animals not killed and helps produce new drugs to reduce human suffering
Clinical trials on humans-potenital harm/side effetcs
Vaccines may continue high risk activities and still develop/pass on pathogens
Use of drug- potentially dangerous sie effects
Suggest some points to consider when evaluating methodlogy relating to the use of vaccines and monoclonal antibodies
Was the sample size large enoguh to be representive
Were particpants diverse in terms of age,sex,ethnicity and health status
Were placebos /control groups used for comparison
Was the duration of the study long enought o show long term effects
Was the trial double nlind (nether doctor nor paiteint knew who was given the dyrg or placebo)to reduce bias
Suggest some points to consider when evaluating evidence and date relatong to the use of vaccines and monoclonqal antiodies
What side efects were pbserved, and how frequent did the y occur
Was a statistical test used to see if there was a sgnificant diff between start and final results
Was the standard devoation of final results large ,shjwoing there may not be a sig diff
What dosage was optimum?Does incfreasing effectiveness epugh to justify extra cost?
Was the cost of production and distrubtion low enough