C2- Cell biology Flashcards
What are the 4 main types of slide preparation?
Wet mount- Specimen submerged in water and cover slip added
Dry mount- Specimen placed onto slide directly and cover slip placed on top
Squash slides- Wet mount prepared and cover slip is used to squash the cells
Smear slides- Edge of a slide is used to create a smooth thin layer of cells over a slide.
What is magnification
the number of times larger an
image is compared with the real size of the object.
What is resolution
the ability to distinguish between
two separate points. If two points cannot be resolved
they will be seen as one point, eg. like car headlights
Light Microscope advantages (5)
Can be used to look at cells and large organelles within cells
Staining cells makes organelles clearer
Preparation quick and simple
Natural colour of material observed
Living tissues can be observed
TEM vs SEM
TEM passes a beam of electrons through the specimen
SEM fires a beam of electrons across the surface, which
are reflected, and then collected
Transition electron microscopy
2D image
Max Magnification = x 500,000
Better resolving power– 0.5nm
Scanning electron microscopy
3D image
Max Magnification =x 100, 000
Less resolving power = 3-10nm
Methylene Blue stain
Positively charged dye attracted to negatively charged molecules
Stains DNA
Differential staining
Used to distinguish between 2 types of organisms, or organelles within an organism
Positively charged stains
Crystal violet
Methylene Blue
Attracted to negatively charged materials in the cytoplasm
Dry mount
used with whole or sectioned specimens
Can see living organisms
Mounts are temporary unless you seal the coverslip
Wet Mount
Specimens suspended in liquids such as oil or water
Cover slip placed at an angle
Greater refraction due to the liquid
-> Greater magnification and resolution
Squash slide
Wet mount first prepared
Gently press down on cover slip
Good for softer samples such as roots
Smear slide
Edge of a slide is used to smear a sample creating a thin even coating
Cover slip then placed
Negatively Charged Dyes
Congo Red
Nigrosin
Repelled by negatively charged cytosol
-> Stays outside cells, makes them stand out
Differential staining
Aids distinguishing between organisms or organelles
Gram stain technique
Acid fast technique
Prepared slide types (4)
1- Fixing= formaldehyde used to preserve
2- Sectioning= Dehydrate, wax and then slice with a microtome
3- Staining
4- permanent mounting
Cytoplasm- Structure
Contains Enzymes
Fluid = Cytosol
Cytoplasm- Function (3)
Where chemical reactions for cells take place
Holds membrane bound compartments (organelles)
Metabolism
-> Catabolism+ Anabolism. Break down and building of molecules
Nucleus- Structure (4)
Dark patches= Chromatin
Double membrane= nuclear envelope
Nuclear pores -> RNA can leave though as DNA too large
Nucleolus inside
Nucleus- Function (4)
Contains genetic material
Chromatin= histones (proteins) forms complex with DNA. Coils and then condenses into chromosomes
Contains instructions to make proteins
When cells divide chromatin condenses to visible chromosomes
Nucleolus (4)
- Inside Nucleus
-Composed of proteins + RNA
-Produces ribosomes
- RNA used to produce ribosomal DNA (rRNA) combined with proteins to make ribosomes
Mitochondria- Structure (4)
- 2 membranes separated by a fluid filled space
- Inner membrane folded to cristae. The inner fluid is the Matrix
- Membrane holds respiration energy
-Own DNA (mtDNA) and own enzymes