Experiments Flashcards
To test a food for starch
IODINE
- turns yellow/red to blue/black
Note : use test tube of water as control
To test a food for fat
BROWN PAPER
Fat is present if a permanent translucent stain is present
To test for reducing sugar (glucose)
BENEDICTS SOLUTION
- add sucrose to water +dissolve
- apply HEAT but do not boil
Blue to brick red
To test a food for protein
BIURET TEST
sodium hydroxide
+ copper sulphate
- blue to purple
To prepare a plant cell (onion)
- forceps: thin, transparent epidermis
- add iodine stain
- drop water : prevent drying out
- coverslip at 45^ angle to eliminate air bubbles
To prepare an animal cell (cheek cell)
- cotton bud: collect cheek cells
- spread on glass slide
Methylene blue: stains nucleus deep blue - water: prevents drying out
- lower coverslip at angle to avoid bubbles
Steps involved in using a microscope
1: slide on stage + clip in place
2: switch on light source
3: use COARSE FOCUS KNOB to bring LOW POWER OBJECTIVE LENS into focus
4 use FINE FOCUS KNOB for HIGH POWER OBJECTIVE LENS
To demonstrate action of osmosis
VISKING TUBING: selectively permeable membrane
- sucrose and water gained in mass and fullness. Water entered visking tubing due to osmosis
Enzyme activity experiments
Enzyme
Substrate
Product
Catalase (liver and celery)
Hydrogen peroxide
Water and oxygen
To investigate the effects of pH on the rate of Catalase activity
- pH buffer and washing up liquid (traps oxygen released-forms foam)
- blend celery + add water + filter solution
- hydrogen peroxide (substrate) to beaker
- water bath at 25^ C
- add HP to catalase solution
- note and record volume of foam after 2 mins
pH 9 was OPTIMUM
To investigate the effect of temperature on the rate of catalase activity (enzyme activity)
- ph buffer 9, blended celery
- hydrogen peroxide (substrate) in different temp water bath
- pour in together
- add washing up liquid - shows foam
- note and record level of foam after 2 mins
20-30^C is OPTIMUM TEMPERATURE
Effect of heat denaturation on catalase activity
- pH buffer 9, blended celery
- boil 1/2 solution for 10 mins
- unboiled catalase = control
- hydrogen peroxide to beaker
- water bath of 25^ C
- add washing up liquid
BOILED = NO FROTH as DENATURED
unboiled = froth
To investigate the influence of light intensity on the rate of photosynthesis
- ELODEA: water plant : can see bubbles of O2 from photosynthesis
- SODIUM BICARBONATE in excess: constant supply of CO2
- water bath - temperature stays constant
- cut elodea at angle
- buffer solution pH 7 - maintains pH
- allow to stabilise , then count O2 bubbles
- move lamp closer - increase light intensity - bubble production increases
Prepare and examine a transverse section of a dicot stem
BEGONIA: non woody herbaceous- easier to cut
- use scalpel to cut section of stem
- wet blade (reduces friction) thin section (allows light through) , cut at right angle
- store on clock glass w water - hydration
- cover slip at angle - no bubbles
Iodine if need more visible
Why use a coverslip ?
To protect lens