Exam 09.01.2026

  1. Vitrification and Plunge Freezing
  2. Why is the emission wavelength longer than the wavelength of absorbed light? What is this phenomenon called? What is fluorescence timeline?
  3. What is confocal of microscopy? What are the types, advantages, and disadvantages?
  4. Gram staining. Cell wall of a gram-negative.
  5. Draw the Epifluorescence setup with the basic components
  6. Stereomicroscope. What is the advantages and disadvantages
  7. Immunofluoresence, how would you label
  8. What information can be found on the objective
  9. Brightfield microscopy
  10. Köhler illumination
  11. Label the parts of microscope