bio paper 1 Flashcards
1st step of microscopy prac
add drop of water to clean slide
step 2 of microscopy prac after adding drop of water to clean slide
add onion epidermal/human cheek cells on slide in water
3rd step of microscopy prac after adding cells onto slide
highlight cells using iodine stain for onion
methylene blue for cheek
4th step of microscopy prac after stain
Put cover slip on top of specimen
1st step of viewing cells micro prac
place slide onto stage and clip into place
2nd step of viewing cells micro prac after placing s/clipping slide on stage
select lowest power objective lens so lowest magnification
3rd step of viewing cells micro prac after choosing lowest power objective lens
looking in eyepiece move stage up/down using coarse adjustment knob till image becomes more focused
4th step of viewing cells micro prac after adjusting coarse adjustment knob
use fine adjustment to further focus until clear
5th step of viewing cells micro prac after using fine-adjustment knob
change to higher power objective lens and refocus if higher magnification needed
1st step on aseptic bacteria prac
pour hot agar into sterile petri dish and let set and cool
2nd step of aseptic prac after pouring hot agar into sterile petri dish
use sterile dropping pippete to evenly spread bacteria
3rd step of aseptic prac after using sterile dropping pippete
soak paper discs in diff conc of antibiotics/septics for same time and place on agar plate covered by bacteria
4th step of asep prac after adding paper antibiotic discs to agar
place disk soaked in sterile water as a control
5th step of asep prac after setting up water control disc
tape lid lightly on petri dish and incubate upside down on 48 hrs
1st step of osmosis prac
set up test tubes w 10cm3 diff conc sucrose solution with 1 pure water as control/ one 1mol/dm3
2nd step of osmosis prac after setting up test tubes
cut potato into cylinders and measure/record masses using balance
3rd step of osmosis prac after cutting potato into cylinders
put a cylinder in each beaker noting which went into which tube for 24hrs
step 4 of osmosis prac after putting cylinders into test tubes for 24 hrs
take cylinders out and dry with paper towels then rerecord mass
1st step of amylase prac
place drop of iodine solution in each cavity of a spotting tile
2nd step of amylase prac after dropping iodine in cavity
place test tube with 2cm3 amylase and 1cm3 of known ph buffer solution in 35 deg water bath
3rd step of amylase prac after putting buffer/enzyme in 35 dg water bath
place another test tube with 2cm3 starch solution in water bath
4th step of amylase prac
pour starch into amylase and buffer solution and start timer while all are in water bath
5th step of amylase prac after mixing all solutions in water bath
every 10s add 1 drop of solution to iodine on spotting tile
colour observation in amylase prac
blue black if starch is present
orange -brown if starch is digested to maltose
what indicates faster rate of reaction in amylase prac
quicker it takes for spot to remain orange-brown
6th step of amylase prac
repeat using diff ph buffers to see effect rate of starch breakdown
how to prepare food test
crush food using pestle and mortar
dissolve some in distilled water
filter out any remaining solid using filter paper lined funnel
reducing sugars step 1
add few drops of benedicts to test tube with food sample
2nd step of reducing sugars test after adding benedick to sample
put test tube in water bath at 80 deg for 5 mins
colour change in benedicks
blue—->green/yellow/brick red
starch test
add few drops of iodine to sample and gently shake
colour change in starch test
browny orange——>blue black
protein test
add biuret solution to sample and shake
colour change in protein test
blue—–>purple
lipid test
add few drops of ethanol and distilled water to sample and shake
colour change for lipid emulsion test
colourless—->cloudy white emulsion
1st step of pondweed prac
add piece of fresh cut pondweed in boiling tube with sodium hydrogen carbonate solution
2nd step of pondweed prac after adding it to boiling tube
place tube 10cm away from lamo
3rd step of pondweed prac after placing tube 10cm away from lamp
switch on lamp and leave on 5 mins and count bubbles per min
4th step in pondweed prac after switch on lamp for 5mins
repeat count 2x more to find mean bubbles per min
6th step of pondweed prac after finding mean bub per min
repeat with boiling tube at diff distances to lamp
how can you control temp gain from lamp in pondweed prac
-use led bulb
-put glass tank with water in between
how do you get more accurate results in pondweed prac
collect o2 bubbles using inverted funnel and vol of gas using syringe