1.1 Laboratory Techniques Flashcards

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1
Q

What is a hazard

A

Anything that poses a potential threat to an individual or the environment

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2
Q

What is a risk

A

The likelihood of harm arising from exposure to a hazard

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3
Q

What is a risk assessment

A

A full consideration of all the hazards and the potential risk with controls that can be taken to minimise the risk

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4
Q

What is a linear dilution

A

When a series of dilutions differ by an equal interval

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5
Q

What is a serial dilution

A

When a series of dilutions differ by a constant proportion

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6
Q

What is a standard curve used for

A

To determine the concentration of a solution

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7
Q

What do buffers do

A

Allow the pH of a reaction mixture to be kept constant

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8
Q

What is centrifugation used for

A

To separate substances of differing density

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9
Q

What are the 2 different types of chromatography

A

TLC and Affinity

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10
Q

What is TLC used for

A

Separating substances based on thing such as amino acids and sugars

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11
Q

What is affinity chromatography used for

A

Used for separating proteins

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12
Q

Name the 2 types of gel electrophoresis

A

Native gel and SDS page

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13
Q

What is gel electrophoresis used for

A

Separating proteins and nucleic acids

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14
Q

What is native gal electrophoresis used for

A

Separating proteins based of off their shape, size and charge and does not denature the molecule

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15
Q

What is SDS Page gel electrophoresis used for

A

Separating proteins based on size alone

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16
Q

How does SDS page gel electrophoresis work

A

All proteins are denatured and given a uniformly negative charge

17
Q

What is the iso electric point

A

The pH at which a soluble protein has no net charge/neutral

18
Q

What happens at the IEP

A

They precipitate out of solution

19
Q

What are Immunoassay techniques used for

A

To detect and identify specific proteins

20
Q

What do immunoassays use

A

Stocks of antibodies with the same specificity

21
Q

What are monoclonal antibodies

A

Antibodies that are derived from a single clone of cells and recognise and bind to a single part of an antigen

22
Q

What can bright field microscopy be used to view

A

Whole or parts of an organism, thin sections of dissected tissue or individual cells

23
Q

How does fluorescent microscopy work

A

Uses specific fluorescent labels to bind to certain molecules within cells or tissue. By tagging a particular part of a sample even specific proteins can show up.

24
Q

What is aseptic technique

A

All the systems that are used to eliminate unwanted contaminants when culturing micro-organisms

25
Q

How can a microbial culture be started

A

Using an inoculum of cells on an agar medium

26
Q

Name a benefit of growing cells in a culture

A

They are much more easily manipulated

27
Q

What does a medium that promotes the growth of animals cells contain

A

Growth factors from serum

28
Q

What is a primary cell line

A

Can divide a limited number of times & derived from normal tissue

29
Q

What is a tumour cell line

A

Can perform unlimited division & derived from tumors

30
Q

What is vita staining used for

A

To identify and count viable cells

31
Q

What is a haemocytometer

A

Used to estimate cell numbers in a liquid culture. (Direct cell count can then be used to calculate cell density)

32
Q

Give 2 disadvantages of a haemocytometer

A

Dead cells are not distinguished from live cells, and it is time consuming