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Modern Cell Theory
energy flow occurs w/in cells
herditary info is passed from cell to cell
all cells have same basic chem composition
Cristae
inner mitochondrial matrix
nucleolus
where ribosomes are made
ER
lipid synthesis
golgi
complex involved in modifying, sorting, and packaging proteins or lipids for secretion or delivery to other organelles.
lysosome
special enzymes to break down macromolecules to be used in other parts of cell
peroxisome
oxidative breakdown of toxic molecules
compartmentalization
allows for increased rxn speed and protection
Bacteria (E. coli)
proteins similar to euk
short generation time
fungal models (yeast)
cell cycle regulation - similar to humans
plants model organisms
arabidopsis thaliana
zea mays - jumping genes
algae model organism
chlamydomonas
Roundworms (c. elegans)
trnasparent, not a lot of tools available, cell death
Fruit flies (drosophila)
multicellular, short regeneration time, immune system, have almsot all genes in humans
-cant freeze, can lose mutation if they die
zebrafish (danio rerio)
embryonic development - develops outside, see through, easy to breed
-vertebrates - more rules
Mice (mus musculus)
best for human learning, longer gen. time, not many marker chromosomes
western blot
detect specific proteins in a sample through gel electrophoresis and transfer to a membrane, followed by antibody binding.
co-immunoprecipitation
a technique used to isolate and study protein-protein interactions by using an antibody to capture a specific protein along with its binding partners.
colocalization
tells if proteins are in same general area - NOT if they interact or close enough to interact - CELLS DEAD (using anit-bodies)
FRET - fluorescence resonance energy transfer
tells if protein comes close enough to interact - 2 proteins w/ two fluorophores, shine light to excite one, lets out color, if theyre close the energy is accepted by other fluorophore and it emits different color
FRAP - fluorescence recovery after photobleaching
overwhelm protein with laser, eliminates fluorescence, observe over time and see if fluorescence returns, if it recovers it means it moves a lot
photoactivation fluorescence microscopy
see where group of proteins that are illuminated move