PCR Flashcards

1
Q

enumerate the steps of PCR

A
  1. denaturation
  2. annealing
  3. extension
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2
Q

this step involves heating the reaction mixture to — the DNA, separating the double-stranded into single strand. what is the temp for this step?

A

DENATURATION
94-98C

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3
Q

the temperature is lowered around — to allow primers to anneal (bind) to their complementary sequences on the single stranded DNA template.

A

50 - 65 C

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4
Q

the temperature is raised to —, and the DNA polymerase extends the primers by adding nucleotides, thus — new DNA strands

A

72-75 C
synthesizing new DNA strands

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5
Q

the steps of PCR are repeated for — to achieve a significant amplification of the target DNA

A

20-40 cycles

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6
Q

maxter mix iincludes all the reagents required for PCR such as — enumerate!

A
  • DNA template
  • primers
  • DNA polymerase
  • nucleotides
  • buffer
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7
Q

enumerate the key condiserations in preparation of PCR master mix

A
  • reagent concentrations
  • total reaction volume
  • mix preparation
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8
Q

total volume of PCR is typically —

A

20-50 uL

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9
Q

enumerate the principles in primer design (6)

A
  • primer length
  • GC content
  • melting temp
  • avoiding self complementarity
  • specificity
  • GC clamp
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10
Q

primer length

A

18-24 nucleotides

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11
Q

GC content

A

40-60%

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12
Q

melting temperature

A

2C each other

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13
Q

adding a GC-rich region at the 3’ end can enhance?

A

primer stability

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14
Q

factors needed to be considered in PCR reaction (6)

A
  • template DNA
  • cycling conditions
  • positive and negative controls
  • reaction volume
  • thermal cyclers
  • data analysis
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15
Q

preferred template DNA

A

purified DNA with minimal contaminants

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16
Q

purpose of positive and negative control

A
  1. to check contamination
  2. ensure the reaction is working
17
Q

after PCR, the amplified products can be analyzed by?

A
  1. gel electrophoresis
  2. real-time PCR
  3. sequencing

to verify the presence of the target DNA

18
Q

materials needed for PCR

A
  • PCR reagents (DNA pol, dNTPs, buffer)
  • microcentrifuge tube
  • electrophoresis equipment
  • agarose gel and buffer
  • DNA ladder marker
  • Gel electrophoresis staining solution
  • pipettes and tips
  • safety equipments
  • DNA template
  • forward and reverse primers
19
Q

portion of DNA to make several copies

A

amplification