topic 1 cell structure Flashcards
light microscope resolution and magnification max
-resolution- 0.2um
- mag - x1500
nucleus and mitochondria can be seen
methods for sample prep
-dry mount - specimen placed directly
- squash slides - wet mount is prepared and cover slip is pressed to squash cells
- smear slides- edge if slide is used to smear sample to create thin even coating
- wet mount- small drop of water in centre of glass slide, forceps is used to place thin layer of specimen onto water, few drops of stain, cover slip
what is differntial staining
using more than one chemical stain
using light microscope
-clip microscope slide onto stage
- select objective lens to lowest power
- use coarse focus to bring the stage just below the objective lens
- look down eyepiece and use the coarse focus to move stage downwards until image is roughly in focus
- use fine focus to make image clearer
- if a higher magnification is needed swap to a more powerful objective and refocus
what to include in biological drawings and what not to
✅title
✅magnification or scale
✅sharp pencil
✅smooth continuous lines
✅include labels
✅include accurate sizes of observable structures
❌shading or colouring
❌arrowhead for labels
❌lines overlapping
magnification
how many times larger an image is than the object
resolution
the ability to distinguish between two separate points
image size
how large the object appears when you view it through a microscope
magnification formula
image size/ object size
cm to mm
mm to um
um to nm
x10
x1000
x1000
nm to um
um to mm
mm to cm
➗1000
➗1000
➗10
eyepiece graticule
small scale placed within the eyepiece used to measure length or width of a specimen
a stage micrometer
used to calibrate the eyepiece graticule and is a glass slide with a scale measured in um
how to graticule is calibrated
- fix the stage micrometer into place on the stage
- look through the eyepiece to line up the micrometer and the graticule
- count the number of graticuke divisions that fit into one micrometer divison
- use the formula to calculate the size of each graticule division at that magnification
graticule division = size of one micrometer division / number of graticule divisons
2 types of electron microscope
- transmission electron microscope (TEM)
- scanning electron microscope (SEM)
TEMs
-use electromagnets to transmit electrons through a specimen. the denser parts absorb more electrons so appear darker in the image formed
- specimen must be viewed in a vaccum
- specimen must be thin
- resolution - max of around 0.5um
- magnification- max of around x1 500 000
SEMs
-scan a beam of electrons across the surface of a specimen. reflected electrons are used to form an image
- produce 3D images of the surface of specimen
- only view non living or dead specimen
- can view thicker specimen
- requires specimen to be coated in a metal ( leads to artifacts)
- max resolution 5nm
-max mag 1500 000
laser confocal microscopy
-a type of fluorescence microscopy
-uses a laser bean to scan a specimen that has been tagged with a fluorescent dye. the dyed components give off light which is focused through a pinhole and onto a detector.the detector is connected to a computer which generates an image. it can be 3D
- less resolution than electron but more than light
- can be used to look at different depths within a specimen and living
nucleus
-contains genetic info in the form of chromosomes
-contains structure known as a nucleolus surrounded by nuclear envelope containing pores
-controls cells activities
-synthesis of ribosomes
-exchange between nucleus and cytoplasm
cell surface membrane
- found on the surface of animal cells
- mainly made up of lipids and proteins
- controls movement of substances into and out of the cell
- partially permeable
- cell signalling
mitochondria
double membraned organele where aerobic respiration takes place and ATP is produced
mitochondria is made up of
-outer membrane - controls the entry and exit of materials
-inner membrane - folded into cristae to increase surface area for respiration enzymes.Cistae project into liquid matrix.It is coated with enzymes which catalyse aerobic respiration reactions to produe ATP.
-matrix- the central space containing enzymes for the Krebs cycle, mitochondrial DNA, and ribosomes.
ribosmes
-ribosomes are the site of protein synthesis and is involved in the process of translation.They are composed of rRNA and proteins and are found either free in the cytoplasm or attached to the rough endoplasmic reticulum.
-ribosomes consist of 2 subunits (large and small) that come together during protein synthesis
-ribosomes read the mRNA sequence during translation to assemble amino acids into a polypeptide chain, creating proteins
-free ribosomes synthesize proteins used within the cell
ribosomes on the RER synthesize proteins for secretion or for use in membranes
-not surrounded by a membrane
golgi apparatus
the golgi apparatus is composed of fluid filled, flattened membrane bound sacs (cisternae).Also contains smaller vesicles
-modifies proteins and lipids recieved from the endoplasmic reticulum, sorts them and packages them into vesicles for transport
-essential for secretion of hormones, enzymes and other molecules
rough endoplasmic reticulum
-The RER is contains a network of membranous sacs called cisternae and tubules and have ribosomes attached to the outer surface enabling protein synthesis
-synthesizes proteins
-proteins enter the RER lumen for folding and initial modifications
- packages proteins into vesicles for transport to the Golgi apparatus