Monoclonal Antibodies Flashcards

1
Q

What are monoclonal antibodies?

A

Antibodies produced from a single clone of cells

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2
Q

What is the first step of producing monoclonal antibodies?

A
  1. Mice are injected -> stimulate production of lymphocytes to make antibodies

Lymphocytes make antibodies but cannot divide to make clones

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3
Q

What is the second step of producing monoclonal antibodies?

A

Tumour cells are cultured.

They can divide to form clones.

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4
Q

What is the third step of producing monoclonal antibodies?

A

Lymphocytes are fused with the tumours cells to create hybridoma cells

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5
Q

What is special about these hybridoma cells?

A

They can divide to make a large number of clones as well as produce antibodies.

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6
Q

What is the fourth step of producing monoclonal antibodies?

A

Monoclonal antibodies produced, collected, purified for use.

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7
Q

What can monoclonal antibodies be used for?

A

Research, treatment, diagnostic testing

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8
Q

How can specific molecules be found using monoclonal antibodies?

A

Monoclonal antibodies used to bind them to a fluorescent dye

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9
Q

How can monoclonal antibodies be used for treatment?

A

Can deliver toxic chemicals and drugs -> harm harmful cells. (e.g to cancer cells)

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10
Q

What is the hormone produced by pregnant women?

A

HCG

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11
Q

What can monoclonal antibodies be used to measure?

A
  1. The levels of a particular chemical in the blood
  2. Pathogens
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12
Q

How can monoclonal antibodies be used to detect HCG?

A

Used to detect HCG in a pregnant woman’s urine

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13
Q

Describe how monoclonal antibodies can be used to detect HCG levels in a pregnant woman’s urine.

A
  1. Urine applied to stick
  2. Stick contains monoclonal antibodies specific to HCG, attached to a dye
  3. If HCG present, monoclonal antibodies cause line of dye to appear.
  4. A second line appears in control zone - shows test is valid, even if result is negative.
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14
Q

Why are monoclonal antibodies not widely used?

A

They produce many side effects

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15
Q

How do bacteria multiply?

A

Binary fission

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16
Q

Under the optimum temperature and nutrient levels, how fast can bacteria divide?

A

Double every 20 mins

17
Q

What 2 ways can bacteria be grown?

A
  1. In nutrient broth (solution)
  2. As colonies in agar gel plate
18
Q

What is important for growing uncontaminated cultures of bacteria?

A

Aseptic technique

19
Q

What 3 steps should be done before culturing?

A
  1. Sterilise culture media, agar plate
  2. Disinfect table
  3. Pass inoculating loop through blue Bunsen flame, allow to cool slightly
20
Q

Name the steps of culturing microorganisms.

A
  1. Sterilisation
  2. Dip inoculating loop into culture
  3. Inoculate agar plate by streaming inoculating loop across surface
  4. Tape lid shut, place in incubator
  5. Sterilisation
21
Q

What is good aseptic technique for the incubation of agar plates during culturing?

A
  1. Do not create airtight seal
  2. Do not incubate above 25°C
  3. Incubate plates with agar surface downward
22
Q

What is the optimum temperature of pathogen growth?

23
Q

What should be done during sterilisation during culturing of microbes?

A
  1. Inoculating loop passed through blue Bunsen flame, left to cool
  2. Bench disinfected