Unit 1.1 - Laboratory techniques for biologists Flashcards

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1
Q

What is a hazard?

A

A hazard is anything which could cause harm

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2
Q

what is risk?

A

Risk is the likelihood of harm arising from exposure to a hazard

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3
Q

What is a linear dilution?

A

Range of dilutions that differ by equal intervals

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4
Q

what is a log dilution?

A

Range of dilutions that differ by a constant proportion

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5
Q

What is a standard curve?

A

A method used to determine concentration of a solution

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6
Q

What are buffers?

A

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

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7
Q

What is a colorimeter?

A

Equipment used to measure the concentration of a coloured solution or the turbidity (cloudiness).

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8
Q

How does a colorimeter work?

A

It passes a light beam, at a specific wavelength through a cuvette containing a sample

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9
Q

How does a centrifuge separate substances?

A

By density

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10
Q

What are the 3 types of chromatography?

A

Thin Layer chromatography
paper chromatography
affinity chromatography

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11
Q

What is chromatography used for?

A

It allows scientists to identify and or purify the components of a mixture e.g. mixture of amino acids or sugars

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12
Q

Paper and thin layer chromatography process

A
  1. 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
  2. The solvent moves up through the paper and carries components of the mixture
  3. The more soluble components travel the furthest
  4. the less soluble travel the least distance
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13
Q

How is the process of thin layer chromatography different from paper?

A

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

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14
Q

What is affinity chromatography used for?

A

It is used to separate target proteins from a mixture

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15
Q

What is the process of Affinity chromatography?

A
  1. A solid matrix or gel column is created with specific molecules bound to the matrix or gel
  2. Soluble target proteins with a high affinity for said molecules become attached to them as the mixture passes down the column
  3. Other non-target proteins are washed out due to a weak affinity to the molecules
  4. The column is washed with specific molecules, due to the high affinity the target proteins will bind and be removed from the column
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16
Q

Why can tumour cell lines be maintained in a culture for a long time?

A

Tumour cell lines can perform unlimited divisions