AH BIOLOGY UNIT ONE Flashcards

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1
Q

Hazard

A

Something that upon exposure can cause harm

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2
Q

Risk

A

The likelihood of harm caused by exposure to the hazard

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3
Q

Hazards in the lab can include…

A

Toxic/corrosive chemicals, heat or flammable substances, pathogenic organisms and mechanical equipment

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4
Q

A risk assessment involves identifying…

A

Hazards, risks and control measures to minimise the risk

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5
Q

Control measures can include…

A

PPE, appropriate handling techniques and aseptic technique

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6
Q

Log dilution series

A

All dilutions differ by a constant proportion in the series

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7
Q

Linear dilution series

A

All dilutions in the series differ by an equal interval.

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8
Q

How is a linear dilution series made?

A

Combining equal volumes of the same stock with different volumes of a suitable solvent

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9
Q

How is a log dilution series made?

A

Using successive dilutions as the new stock solution

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10
Q

What’s a standard curve’s function?

A

Determining unknown concentration values.

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11
Q

How to make a standard curve

A

Plot measured values for known concentrations and draw a line/curve to connect them all. Then determine your unknowns

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12
Q

What’s the function of a buffer?

A

Reduces the effect of pH as a confounding variable

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13
Q

How does a colorimeter quantify concentration?

A

Determining how much light has been absorbed by a coloured solution by using suitable wavelength filters.

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14
Q

How does a colorimeter quantify turbidity?

A

By determining % transmission of light

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15
Q

A centrifuge separates substances based on what?

A

Density

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16
Q

How does a centrifuge separate substances based on density

A

More dense substances settle in the pellet. Less dense substances stay in the supernatent

17
Q

Paper and thin layer chromatography can separate substances like…

A

Amino acids and sugars

18
Q

The speed that each solute travels along the chromatogram depends on…

A

Its differing solubility in the solvent used

19
Q

In affinity chromatography, a specific matrix or gel column is made with what binding to it?

A

Specific molecules

20
Q

What happens to the soluble, target molecules during affinity chromatography?

A

They stay attached to their matrix/gel column

21
Q

What happens to the weaker, non target molecules in affinity chromatography?

A

They are washed out

22
Q

What is the principle of gel electrophoresis?

A

Separating proteins based on their size/shape

23
Q

In gel electrophoresis, charged macromolecules move through what?

A

An electric field attached to a gel matrix

24
Q

SDS page electrophoresis separates proteins based on what alone?

A

Size

25
Q

What happens surfing SDS page electrophoresis?

A

All molecules are given an equally negative charge and denatured