2A Flashcards
what is magnification
how much bigger a sample appears to be under the microscope than it is in real life
what is resolution
the ability to distinguish between two points on an image.
what are the advantages of an electron microscope
the resolution in x2000 more than LM microscope
it produces detailed images
SEM produces 3D image
what are the disadvantages of an electron microscope
Samples have to be placed in a vacuum
very expensive
need to be highly skilled to create samples
complex staining process
image may contain artefacts
what is the equation for magnification
magnification=size of image/size of the object
What do Transmission electron Microscope do
pass a beam of electrons through the sample.
What are the limitations of a Transmission electron microscope
Thin sections of specimen are needed for TEM as the electrons have to pass through the specimen for the image to be produced
flat 2D image
What do Scanning electron microscopes do
pass a beam of electrons over the surface, the electrons are then reflected off the surface of the specimen
what are the limitations of scanning electron microscope
The resolution is lower then that of the transmission electron microscope
what is cell fractionation
The process where cells are broken up and the different organelles they contain are separated
what is cell fractionation used for
Used to help us study cell structure and function
what is momogenisation
breaking up the cells
what is a centrifuge used for
separating the cell components
Before cell fractionation can begin what must happen
the tissue is placed in, cold, isotonic, buffer solution
why must the tissue be cold
to reduce enzyme activity, which may break down organelle
what is the role of isotonic solution
to prevent the organelle from bursting/ shrinking due to osmotic gain/ loss of water
what is the role of the solution being buffered
to maintain a constat PH
what is differential centrifugation and why does it happen in the experiment.
The size and density of any organelle is relatively constant so they all separate at a specific speed. Since the whole process involves centrifuging at different speeds it is called differential centrifugation.
In what order is the organelle separated during centrifugation
it happens in the order of most to least dense. Nuclei, chloroplast and mitochondria, lysosomes and endoplasmic reticulum, ribosomes
what is a graticule
a series of fine lines in the eyepiece of an optical device, such as a microscope, used as measuring scale. It enables scientists to estimate accurately the size of objects viewed under a microscopes.
does not change in size
what are the steps of cell centrifugation
1 chop up fresh tissue in ice cold, isotonic buffer solution.
2 Put the chopped tissue in a blender or homogeniser to break open the cells.
3 Filter the mixture to remove the debris, such as connective tissue and plant cell walls.
4 Pour the mixture into tubes and spin very quickly in a centrifuge.
5 The liquid layer on the top ( the supernatant ) is poured in to a fresh tube, leaving the pellet behind.
6 The supernatant may then be spun again at a faster rate to produce a sediment containing mitochondria and at an even higher speed for other organelle
what is the supernatant
The liquid layer on the top off the pellet, in centrifugation.
what is the cell membrane made out of
Phospholipids
How to prokaryotic cells differ from eukaryotic cells
Prokaryotic cells do not have a nucleus, whereas eukaryotic cells do. Prokaryotic cells also do not have a cell membrane
what are prokaryotic, plant and fungal cell walls made from
prokaryotic- peptidoglycan
fungal- chitin
plant- cellulose
what is a plasmid
a circular loop of DNA that contains their genetic material
what is a nucleoid
A space within a prokaryotic cell where DNA is found
what is the procedure for the calibration of a cell
1 put in the eyepiece
2 put on the stage micrometer
3 align them to calibrate
4 count divisions on the EPG = how many divisions on the micrometer
5 with the scale of the micrometer, find the length of each division on the EPG ( division on micrometer/divisions on EPG)
6 remove micrometer from stage
7 Put a cell slide on the stage
8 Measure EPG division that a cell accounts for
9 cell length = length of each division on EPG x number of EPG divisions of cell.
what is the structure and function of a nucleus for eukaryotic cells
structure: surrounded by a nuclear envelope (double membrane with pores), and it contains chromosomes (genetic material) and a dense solid structure called a nucleolus which is involved in ribosome synthesis.
Function: It contains the genetic information for the cells (including chemical reactions and cell division). It also controls when mRNA is produced, and hence controls protein production.
What is the structure and function of the different types of endoplasmic reticulum in a eukaryotic cell
structure: surrounds the nucleus, rough ER has ribosomes, smooth ER doesn’t
function of rough ER: site of protein synthesis
function of smooth ER: site of lipid and carbohydrate metabolism including hormone synthesis.