Lab Exam 2 Flashcards

(26 cards)

1
Q

What does PCR stand for

A

Polymerase chain reaction

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2
Q

What are the functions of primers?

A

To determine what region of DNA will be amplified

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3
Q

What is the function of taq polymerase

A

Automates the repetitive step of amplifying specific DNA sequences

5’———->3’

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4
Q

What is the function of buffer in PCR

A

Keeps polymerase “happy”

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5
Q

What are free bases

A

DNA nucleotides to make the new DNA

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6
Q

What is gel electrophoresis

A

Used to separate DNA, RNA, macromolecules and protein fragments based on size and charge

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7
Q

What is an agrose gel made from

A

Polysaccharide extract from seaweed

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8
Q

What dictates how fast DNA moves through an agarose gel?

A

Size of DNA
Small= faster large = slower

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9
Q

Do high percentage agarose gels have smaller or larger holes

A

Smaller holes

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10
Q

What does ELISA stand for

A

Enzyme- Linked Immunosorbent Assay

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11
Q

Give a real world example of an ELISA test

A

Diagnosing HIV or Lymes

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12
Q

What color is bromocresol green in acidic conditions

A

Yellow

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13
Q

What are the four key components of MacConkey Agar?

A

Peptones, lactose, bile salts, and crystal violet

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14
Q

Do you expect gram + or gram - bacteria to grow on MacConkey Agar

A

Gram -

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15
Q

What is prevalence

A

% of population with disease

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16
Q

What is incidence

A

Total number of cases

17
Q

What is CFU

A

Colony forming unit

18
Q

Why are calculating CFUs important in understanding infections

A

Calculates number of viable bacteria or fungi in sample, indicates severity of disease

19
Q

What is 16SrRNA

A

Part of a small ribosome

20
Q

What is the 16SrRNA gene used for sequencing and identifying species of bacteria?

A

Each species has a unique 16s RNA sequence

21
Q

What is alpha hemolytic activity

A

Partial RBC lysis

22
Q

What is the beta hemolytic activity

A

Complete RBC lysis

23
Q

What is gamma hemolytic activity

24
Q

Why and how is Snyder media selective and differential

A

Selective because media is acidic which kills non-acidophile bacteria

Differential because bromocreasal green turns yellow is very acidic conditions

25
26
What are the steps of PCR
1)melting 90-95 •c - melts DNA strands apart 2) annealing (aka primer binding) 50-60•C primers anneal to single stranded DNA 3) elongation 72•C - Taq polymerase makes new DNA