Unit 1.1 - Laboratory techniques for biologists Flashcards
What is a hazard?
A hazard is anything which could cause harm
what is risk?
Risk is the likelihood of harm arising from exposure to a hazard
What is a linear dilution?
Range of dilutions that differ by equal intervals
what is a log dilution?
Range of dilutions that differ by a constant proportion
What is a standard curve?
A method used to determine concentration of a solution
What are buffers?
solutions that very little change to ph occurs when a small volume of acid or base is added. This allows the ph of a reaction mixture to be kept constant
What is a colorimeter?
Equipment used to measure the concentration of a coloured solution or the turbidity (cloudiness).
How does a colorimeter work?
It passes a light beam, at a specific wavelength through a cuvette containing a sample
How does a centrifuge separate substances?
By density
What are the 3 types of chromatography?
Thin Layer chromatography
paper chromatography
affinity chromatography
What is chromatography used for?
It allows scientists to identify and or purify the components of a mixture e.g. mixture of amino acids or sugars
Paper and thin layer chromatography process
- A sample of the mixture to be separated is placed on a dot near the bottom of a strip of chromatography paper which is placed in a solvent
- The solvent moves up through the paper and carries components of the mixture
- The more soluble components travel the furthest
- the less soluble travel the least distance
How is the process of thin layer chromatography different from paper?
TLC is carried out the same except it is performed on a sheet of glass or plastic which is coated with a thin layer of adsorbent material, usually silica or cellulose
What is affinity chromatography used for?
It is used to separate target proteins from a mixture
What is the process of Affinity chromatography?
- A solid matrix or gel column is created with specific molecules bound to the matrix or gel
- Soluble target proteins with a high affinity for said molecules become attached to them as the mixture passes down the column
- Other non-target proteins are washed out due to a weak affinity to the molecules
- The column is washed with specific molecules, due to the high affinity the target proteins will bind and be removed from the column
Why can tumour cell lines be maintained in a culture for a long time?
Tumour cell lines can perform unlimited divisions