key area 1 Flashcards

1
Q

linear dilution

A

Concentrations of each solution are separated by an equal interval e.g. 0.1, 0.2, 0.3 (does not have to be a factor of 10

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2
Q

log dilution

A

Dilutions in a log dilution series differ by a constant proportion, for example 10-1, 10-2, 10-3

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3
Q

standard curve

A

Method that is used to determine the concentration of a solution by using known concentrations which are measured and graphed

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4
Q

buffers

A

Sterile solutions which control pH.

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5
Q

colorimeter

A

Device that is used to measure the absorbance of a specific wavelength of light by a solution.

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6
Q

absorbance

A

How much light has been absorbed by the sample.

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7
Q

transmission

A

How much light passed through the sample without being absorbed. % transmission can calculate the turbidity of a substance

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8
Q

centrifugation

A

A process which uses centrifugal forces to separate components of a mixture.

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9
Q

pellet

A

Forms at the bottom (higher density materials) after centrifugation.

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10
Q

supernatant

A

liquid at the top (lower density materials) after centrifugation.

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11
Q

chromatography

A

A set of techniques which separates the components of a mixture.

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12
Q

thin layer chromatography

A

Used for separating amino acids and sugars, a strip of absorbent material on a non reactive binding, the amount they travel depends on the solubility and how much they bind to the stationary phase

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13
Q

affinity chromatography

A

Relies on the binding interactions between a protein and an immobilised ligand. Use to separate proteins.

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14
Q

paper chromatography

A

uses pigments in a leaf, polar components will bind to cellulose fibres quickly and don’t travel up the paper

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15
Q

electrophoresis

A

A process which applies an electric current across a gel to separate components of a mixture.

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16
Q

native gel electrophoresis

A

Type of electrophoresis which separates proteins by their shape, size and charge.

17
Q

SDS page electrophoresis

A

Type of electrophoresis which separates proteins by size alone.

18
Q

isoelectric point

A

The pH at which a soluble protein has no net charge and will precipitate out of solution.

19
Q

bright field microscopy

A

Commonly used to observe whole organisms, parts of organisms, thin sections of dissected tissue or individual cells. uses stains to improve clarity

20
Q

fluorescent microscopy

A

Specific fluorescent labels to bind to and visualise certain molecules or structures within cells or tissues.

21
Q

haemocytometer

A

A device which allows an estimation of the concentration of cells in a sample to be made.

22
Q

aseptic techniques

A

Used to eliminate unwanted microbial contaminants when culturing micro-organisms or cells.

23
Q

examples of aseptic techniques

A

blue flame on the loop, chemicals to clean work surface, flame the glass neck of bottles

24
Q

microbial culture

A

Can be started using an inoculum of microbial cells on an agar medium, or in a liquid broth with suitable nutrients.

25
Q

primary cell line

A

A culture which will only divide a limited number of times and then die

26
Q

tumour cell line

A

A culture which does not have limitation, and will grow and divide indefinitely in cell culture.

27
Q

typical cell culture

A

Contains water, salts (Murashige and Skoog salts for plants), amino acids, vitamins and glucose.

28
Q

complex cell culture

A

Contains growth factors (proteins) from serum to promote cell growth and division (proliferation)

29
Q

vital staining

A

Estimates of cell counts can be made can be made using trypan blue dye, which is absorbed by dead cells. Required to identify and count viable cells.

30
Q

immunoassay

A

Techniques which use antibodies linked to reporter enzymes to cause a colour change in the presence of a specific antigen.

31
Q

monoclonal

A

Type of antibodies can be used to detect both the presence and concentration of a protein within a solution.

32
Q

western blotting

A

Allows scientists to identify specific proteins which are present in a cell sample. Technique used after SDS-PAGE electrophoresis where the membrane is then probed for the protein of interest using a specific antibody that is linked to a detectable label.