Labelled Immunoassays

20 questions β€’ 1 test β€’ tap a section to begin

Welcome! 10.3 Labelled Immunoassays β€” Test 1 — 20 questions, CSIR-NET style.

What this test covers

  • Labels: enzyme, radioisotope, fluorescent, chemiluminescent
  • ELISA formats: direct, indirect, sandwich, competitive
  • Standard curves, washing, secondary-antibody amplification
  • RIA vs ELISA; ELISpot; hook effect

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10.3 Labelled Immunoassays β€” Test 1
Q1. Labelled immunoassays improve on simple precipitation/agglutination chiefly by:βœ“ Using a detectable label to greatly increase sensitivity and allow quantitation
Q2. In an enzyme immunoassay (ELISA), the signal is produced when:βœ“ The enzyme label converts a substrate into a coloured product
Q3. A direct ELISA uses:βœ“ A single labelled antibody that binds the antigen
Q4. An indirect ELISA detecting patient antibody uses, in order:βœ“ Plate-bound antigen β†’ patient antibody β†’ labelled anti-immunoglobulin
Q5. A sandwich ELISA for an antigen requires that the antigen:βœ“ Has at least two distinct epitopes for capture and detection antibodies
Q6. A competitive immunoassay is especially useful for measuring:βœ“ Small molecules (haptens) with only one epitope
Q7. Radioimmunoassay (RIA) uses which type of label?βœ“ A radioisotope
Q8. A fluoroimmunoassay uses a label that:βœ“ Emits light of a specific wavelength when excited
Q9. Chemiluminescent immunoassays generate signal by:βœ“ A light-emitting chemical reaction catalysed by the label
Q10. In a competitive ELISA, the signal is:βœ“ Inversely proportional to the amount of analyte in the sample
Q11. The washing steps in ELISA are important to:βœ“ Remove unbound reagents and reduce background signal
Q12. A key advantage of enzyme labels over radioactive labels is that they:βœ“ Avoid radiation hazards and have a long shelf life
Q13. A standard (calibration) curve in a quantitative immunoassay is used to:βœ“ Convert measured signal into analyte concentration
Q14. The 'hook effect' in a sandwich immunoassay causes falsely low results when:βœ“ Analyte is in great excess, saturating both antibodies separately
Q15. Enzyme-linked immunospot (ELISpot) is used to:βœ“ Detect and count individual cells secreting a specific cytokine or antibody
Q16. A secondary (anti-immunoglobulin) antibody is often labelled rather than the primary because it:βœ“ Amplifies the signal and allows one labelled reagent to be used for many primaries
Q17. Compared with agglutination, ELISA is generally:βœ“ More sensitive and quantitative
Q18. A capture (sandwich) ELISA improves specificity because:βœ“ Two antibodies must bind two epitopes of the same antigen
Q19. Which label type is most associated with environmental/safety concerns from radioactive waste?βœ“ Radioisotope (RIA)
Q20. Match each assay/feature with its description and select the correct option.βœ“ A-iv, B-i, C-ii, D-iii