1.1: Laboratory techniques Flashcards

1
Q

Stepwise method of diluting a sample where each dilution is by a factor of 10 e.g. 10^0, 10^-1,10^-2 etc.

A

Log dilution series

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2
Q

A stepwise method of diluting a sample where each dilution is by an equal amount, e.g. 0, 0.2, 0.4, 0.6, 0.8, 1.0 M.

A

Linear dilution series

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3
Q

Graph produced from a number of samples of known concentration. Can be used to determine the concentration of an unknown.

A

Standard curve

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4
Q

Solution used to keep the pH constant during a reaction.

A

Buffer

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5
Q

Apparatus used to estimate the concentration of a solution by measuring the light absorbed by or transmitted through it.

A

Colorimeter

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6
Q

Apparatus used to separate large and small components of a sample due to differences in density.

A

Centrifuge

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7
Q

What is the name for the more dense component in a centrifuge tube and the name for the less dense components in a centrifuge tube

A

Less dense= Supernatant
More dense= Pellet

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8
Q

Technique used to separate proteins or amino acids due to their differential solubility in the solvent and absorption to paper, or other stationary phase.

A

Chromatography

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9
Q

Types of chromatography

A
  • Thin layer
    -Paper
  • Affinity
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10
Q

Charged macromolecules move through an electric field applied to a gel matrix.

A

Gel electrophoresis

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11
Q

What substances can paper and thin layer chromatography be used to separate?

A

Different substances such as amino acids and sugar.

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12
Q

The speed that each solute travels along a chromatogram depends on its what?

A

Its solubility in the solvent used

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13
Q

A separation technique in which soluble target proteins with a high affinity in a mixture become attached to specific molecules as the mixture passes down a column. Non-target molecules with a weaker affinity are washed out.

A

Affinity chromatography.

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14
Q

Electrophoresis gel used to separate molecules by shape, size and charge

A

Native

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15
Q

Electrophoresis gel used to separate molecules by size alone. It does this by giving all molecules an equally negative charge and denaturing them.

A

SDS-page

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16
Q

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

A

Isoelectric point or IEP

17
Q

Technique which uses
antibodies linked to reporter enzymes to cause a colour change in the presence of a specific protein antigen.

A

Immunoassay

18
Q

Antibodies that are all specific for a particular protein

A

Monoclonal antibodies

19
Q

“Labels” used to detect an antibody joined to a protein antigen

A

Reporter enzyme OR Fluorescence OR Chemiluminescence.

20
Q

Technique in which labelled antibodies joined to specific proteins are immobilised on a membrane.

A

Western blotting

21
Q

Microscopy technique used to examine whole organisms, parts of organisms or thin sections of stained tissue.

A

Bright field

22
Q

Microscopy technique that allows protein structures to be seen by using a light emitting stain.

A

Fluorescence

23
Q

Cell culture technique that is designed to prevent contamination by micro-organisms.

A

Aseptic technique

24
Q

Ways to sterilise equipment and culture media

A

Heat OR chemicals

25
Microbes or cells used to start a new culture.
Inoculum
26
Slide with microscopic grid used to estimate the number of cells in a sample.
Haemocytometer
27
A stain used to identify viable (living) cells.
Vital stain
28
Stepwise method of diluting a microbial sample to achieve a suitable colony count where each dilution is by a factor of 10. е.g. 10°, 10^-1,10^-2 etc.
Serial dilution
29
Serum proteins essential for an animal cell culture to survive and multiply.
Growth factors
30
Visible mass of microbial cells all derived from one.
Colony
31
Term for animal cell cultures that have a short lifetime as they can only divide a limited number of times.
Primary cell line
32
Animal cell cultures that have a limitless lifetime (immortal) as they can divide indefinitely.
Tumour cell line