Practical Techniques Flashcards
Why does use of a colorimeter improve repeatability of results
It is quantitative and standardises the method
What’s one way a student could ensure a sample is kept at the same temperature the whole way through the experiment
Measure the temperature at intervals and use appropriate corrective measure
What’s the purpose of boiling the agar in the aseptic practical
So no contamination
What’s the purpose of transferring the same volume of liquid culture onto each agar plate in the aseptic practical
So same number of bacteria transferred to allow comparison
Describe how a student could make up a dilution series in bacteria practical
- Add 1 part bacteria culture to 9 parts sterile liquid
- Mix
- Repeat using 9 parts fresh sterile liquid and 1 part of 10^-1 and 10^-2 dilutions to make 10^-3 dilutions
Why does a student not use his preliminary dilution (aseptic practical)
- count is unlikely to be reliable
- because there’s too many cells
Describe method for potato osmosis practical
1) weight first and then put each cut cube in a test tube of sucrose and dilute water solution that you have made up.
2) at room temperature
3) dry the cubes with paper towel to remove excess water before measuring
4) measure mass of cubes every 10 mins
5) calculate percentage change in mass
In chromatography why is pencil used to mark and not ink
The ink and leaf pigments would mix
Describe the method to separate leaf pigments in chromatography
- level of solvent below line
- stop before solvent reaches the top
What is the purpose of incubating the root tip with HCl
- stops cell division from occurring
- hydrolyses the middle of the lamella so that the cells can be separated easily
How do you carry out a serial dilution?
1) Take original solution of known concentration
2) fill additional test tubes with the same volume of distilled water
3) transfer the same volume of solution from one test tube to the next and mix
Describe how to produce and use a calibration curve eg for concentration of protein in urine
- use water and your protein solution to produce a dilution series of known concentrations protein
- measure absorbance of each concentration using a colorimeter
- plot a graph of absorbance on Y axis against concentration on X axis and draw a curve
- use absorbance of samples to find protein conc from the curve
Why must a eyepiece graticule be calibrated when switching to a higher magnification
The stage micrometer will appear larger and so each eyepiece division will be a different value
Suggest why a stage micrometer and an eyepiece graticule are needed
- the size of the units of the eyepiece graticule change depending on the magnification being used
- a stage micrometer can be used to calibrate the graticule
Describe how a student could use an eyepiece graticule to determine the mean diameter eg of stomata
- measure each stoma using eyepiece graticule
- calibrate eyepiece graticule against stage micrometer
- take a number of measurements to calculate a mean