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22 Cards in this Set

  • Front
  • Back

Compound Light Microscopy

objective lens x ocular lens


= total magnification

Ocular Lens

Remagnifies the image formed by the objective lens


At the top of the microscope, the eyepiece

Body Tube

Transmits the image from the objective lends to the ocular lens


objective > ocular

Objective Lens

Primary lenses that magnify the specimen (the one that rotates)

Stage

Holds the microscope slide in position

Condenser

Focuses light through the specimen

Diaphragm

Controls the amount of light entering the condenser

Illuminator

Light source

Stain

Colorizing a sample with a dye to view it through a microscope

Chromophore

Stains that are salt composed of a positive and a negative ion one of which is colored

Acidic Dye

Negative ions


Less common


Include negrosin, India ink


Basic Dye

Positive ions


Include, crystal violet, methylene blue, malachite green, safrinin, cobalfuchsin

Mordant

Intensifies the stain


Negative staining

Staining the background instead of the cell

Simple Stain

To view shape, size and arrangement


Single basic dye


Stain is applied, washed and dried

Differential Stains

Used to distinguish between bacteria


Gram and Acid Fast

Gram Stain

Positive or negative


Positive cells have a thick peptidogylcan cell wall


1. Primary Stain (purple)


2. Mordant (purple)


3. Decolorizing (colorless)


4. Counterstain (red)


(+) cells are purple (-) cells are red

Acid Fast Stain (Ziehl- Neelsen)

Stains cells that have mycolic acid in their cell walls (waxy)


Used to detect tuberculosis and leprosy


1. Carbolfuchsin (red) added to stain and heated


2. Treated with decolorizer


(cells that turn colorless are acid fast)


3. Counterstain, methylene blue (non acid fast cells turn blue)


Special Stains

Capsule Stain


Endospore Stain


Flagella Stain

Capsule Stain

Negative Staining


Capsule= gelatinous covering


Capsule determines cells virulance


Nigrosin added, repeled by cells but stains background


Safrinin added to stain cells, capsules remain colorless and appear as a halo

Endospore Staining (Scharffer- Fulton)

Regular dyes cannot penetrate endospore


Stain (malachite green) added and heated


Stain washed to remove dye


Safrinin added to counterstain


Result is a green cell within a red/pink cell

Flagella Staining

Difficult to stain flagella


Locomotion to small to be seen w/o staining


Mordant and carbolfuchsin to build up diameter of flagella until visible


(not iodine, potassium aluminum.. maroon color)


Shows the arrangement of flagella