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