Practical

    Cards (16)

    • resolving power (d)

      wavelength/2(NA); can be increased by increasing the NA or decreasing the wavelength
    • Microscope parts
    • parfocal
      the focal point is the same for all lenses, and switching lenses requires only minor adjustments
    • plate growth characteristics

      shape (circular, irregular, rhizoid); margin (entire or smooth, undulate or wavy, lobate, filamentous, rhizoid); elevation (flat, raised, convex, umbonate); consistency; pigmentation
    • slant growth characteristics 

      abudance; pigmentation; optical characteristics; form (filiform, beaded, echinulate, spreading, arborescent, rhizoid)
    • broth growth characteristics

      turbid, pellicle, sediment, flocculent
    • gram stain
      crystal violet (basic stain), gram's iodine (mordant), 95% ethanol (decolorizer), safrinin (counterstain)
    • PRB tubes
      differential medium consisting of a durham tube, phenyl red (pH), peptones, and specific carb
    • PRB results
      acid production from carb fermentation lowers the pH and turns the medium yellow; no acid production is replaced by the degredation of peptones into amino acids, which releases ammonia raises the pH turning the medium pink
    • spectrophotometer
      first wipe down cuvette; transfer LB into cuvette and zero it; then transfer culture into cuvette and measure the OD
    • cells/ml
      # of colonies/ dilution X amount plated (ml)
    • titer (pfu/ml)
      # of plaques / dilution X virus quantity
    • litmus milk reactions
      can be alkaline (deep blue), proteolysis (brown w/ purple band), litmus reduction (white w/purple band), or lactose fermentation (pink)
    • litmus milk
      differential medium consisting of lactose (milk sugar), casein, and litmus (pH and redox indicator)
    • ELISA
      coat the wells with different antigens and detect them with an enzyme-linked antibody; the peroxidase enzyme reacts with the substrate to produce a color change to yellow
    • blocking solution
      used to block unoccupied sites to prevent nonspecific binding by the antibodies; done in between the antigen and antibody steps
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