Cells Part 1- Cell Structure And Microscopy Flashcards
Describe how a light microscopes work
Beams of light are condensed to form an image
Focused with a glass lense
What are the advantages and disadvantages of light microscope
Lower mag and reso
Alive, coloured, seen with eye
What is resolution
Minimum distance between 2 points at which can be distinguished from each other
What is magnification
How much bigger than image is than the specimen
What is the wavelength of an electron
0.01 to 0.001 nm
How to transmission electron microscopes work
Beams of electrons pass through the specimen
Parts absorb electrons appear dark
Produces a photo micrograph
What are the advantages and disadvantages of TEM
Smaller objects seen, higher resolution
In vacuum, no living, complex staining technique, extremely thin specimen, artefact, not coloured
How to scanning electron microscopes work
Beams of electrons directed on surface of specimen in a regular pattern
Builds 3D image after analysing pattern scattered electrons that gather in cathode ray tube
How to scanning electron microscopes work
Beams of electrons directed on surface of specimen in a regular pattern
Builds 3D image after analysing pattern scattered electrons that gather in cathode ray tube
What are the advantages and disadvantages of SEM
3D, high resolution, thicker
Vacuum, lower reso then TEM, complex staining, no internal structures seen
What conditions are needed for cell fractionation
Cold- reduce enzyme activity
Isotonic - Same water potential - prevent osmotic damage to organelle
Buffered- prevent denaturing
What are the stages of cell fractionation
1.) Homogenisation- cells are homogenised in a blender to beak them open. The resulting mixture is called cell homogenate (resultant fluid after homogenisation that contains the broken open cells and their components
2.) The homogenate is filtered through a gauze to separate any large cell debris, like connective tissue, from the organelle
3.) Ultracentrifugation- it is centrifuged at various speeds and durations to fractionate the cell components, forming a series of pellets. The heaviest organelles form pellet at the bottom. The supernatant is drained off and spun in a centrifuge at a high speed and the process is repeated
1.Break open cells/tissue and filter
OR
Grind/blend cells/tissue/leaves and filter;
Accept homogenise and filter
2. In cold, same water potential/concentration, pH controlled solution;
Accept for ‘same water potential/ concentration’, isotonic
Accept for ‘pH controlled’, buffered
3. Centrifuge/spin and remove nuclei/cell debris;
4. (Centrifuge/spin) at high(er) speed, chloroplasts settle out;
Why can the same organelle appear differently within the same cell
Cells are a cut/ cross section
Mitochondria are orientated differently
What is an artefact and why should they be minimised
Visible entity that resembles structural detail of specimen
Not a legitimate feature of the specimen
What are the functions of the nucleus
Ribosomal rna- assemble ribosomes
mRNA - protein synthesis
Protect dna and genetic information
Replicate dna for cell division
What is the nuclear membrane for
Outer and inner membrane
Protect and enclose dna
Pores