Intro/Cells Flashcards

1
Q

Define: cells

A

smallest unit of living matter capable of independent existence

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2
Q

How many types of cells are there in the body

A

around 200

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3
Q

Define: tissues

A

Groups of cells and their ground substances that act together to perform a particular function

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4
Q

What is the difference between simple and compound tissues?

A

Simple tissues are made up of all the same type of cell where compound tissues are made of different cell types

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5
Q

What are the main tissue types in the body?

A

Connective, epithelial, muscle, and nerve

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6
Q

Define: organs

A

anatomically distinct groups of tissues, usually of several types, joined as structural unit to perform specific functions

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7
Q

Define: systems

A

primarily groups of organs, which have similar or related functional roles

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8
Q

When is brightfield microscopy suitable? What do the specimens tend to look like?

A

for observing the natural colours of a specimen or the observation of stained samples.
The specimen appears darker on a bright background

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9
Q

When is phase contrast microscopy useful?

A

observing unstained specimens that lack a colour

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10
Q

What is another type of microscopy used to visualized unstained samples?

A

Differential Interference Contrast microscopy

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11
Q

How is Differential Interference Contrast microscopy (DIC) similar and different to phase contrast microscopy?

A

As with Phase Contrast, DIC transforms the phase shift of light, induced by the specimen refractive index, into detectable amplitude differences. However, because DIC utilizes optical path differences within the specimen to generate contrast the 3D appearance may not represent reality

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12
Q

What are the two main groupings of dyes used to stain (mainly) colourless tissues?

A
  1. Basic (cationic) dyes - blue

2. Acidic (anionic) dyes - red

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13
Q

Name an example of a basic dye

A

hematoxylin

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14
Q

Name an example of an acidic dye

A

eosin

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15
Q

How do basic/acidic dyes work?

A

They have either positively or negatively charged colour radicals that will bing with either acidic groups (like phosphates in DNA/RNA) or basic groups (like basic proteins)

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16
Q

Hematoxylin/eosin (H&E) staining stains the nucleus and ribosomes ___, the cytoplasm ___ and collagen ____

A

blue, red, pink

17
Q

define: magnification. How do you calculate it?

A

the number of times lager the image is compared to the true size

image size/actual size

18
Q

define: resolution

A

the ability to distinguish between two points

19
Q

in brightfield microscopy, what is resolution dependent on ?

A

Wavelength

20
Q

What things can you not resolve with brightfield microscopy? why?

A

Things less than ½ the wavelength of light

won’t interfere with the light beam, so you can’t resolve them

21
Q

Why do electron microscopes have a much higher resolution than brightfield microscopes?

A

because electron wavelengths are more than 10,000’s times shorter than light wavelengths

22
Q

What determines the limit of resolution of brightfield microscopes?

A

Numerical Aperture (NA), or the ability of the lens to collect the light

23
Q

in air, the NA will typically be..?

A

less than 1

24
Q

What must be done for lenses with an NA value over 1?

A

need to use oil

25
Q

what is the typical magnification of a light microscope and the theoretical maximal resolution?

A

Typical magnification of a light microscope, assuming visible range light, is ~1000x with a theoretical resolution limit of around 0.2uM

26
Q

What formula can you use to determine resolution for a light microscope?

A

R = 0.5λ/NA

27
Q

What are 4 advantages to light microscopes?

A
  1. Can be done on live cells or dead cells
  2. Can use coloured dyes and fluorescent antibody labeling to distinguish features
  3. Inexpensive
  4. Easy to use
28
Q

What are two limitations of light microscopy?

A
  1. ~200 nm limit of resolution

2. ~1000x magnification limit

29
Q

What are two advantages to electron microscopy?

A
  1. High Resolution Images to ~50pm

2. ~100,000x magnification

30
Q

What are 4 limitations to electron microscopy?

A
  1. Samples must be fixed
  2. No possibility of colour
  3. Expensive
  4. Difficult sample preparation