GEL ELECTROPHORESIS LAB Flashcards

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1
Q

PCR

A

Polymerase Chain Reaction

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2
Q

What does PCR do?

A

PCR isolates small DNA fragments

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3
Q

How does PCR isolate small DNA fragments

A

it uses restriction enzymes and then amplifies the fragments to make large volumes of repeats for clearer study

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4
Q

How many steps are there in PCR?

A

3, denaturing, annealing, and DNA synthesis

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5
Q

What is denaturing

A

Step one in PCR , addition of HEAT to separate the double strands of DNA

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6
Q

What is annealing

A

DNA is rapidly cooled and jpind by PRIMERS to direct which segments are wanting to be amplified

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7
Q

WHat is DNA synthesis

A

DNA replication occursthrough DNA POlymerase on both os the exposed strandsand copies are made until the volume is large enough

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8
Q

Gel Electrophoresis/DNA Fingerprinting

A

Separates fragments of DNA based on SIZE

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9
Q

what is DNA Size?

A

Fragment length= the number of base pairs

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10
Q

what decides the movement?

A

polarity/ electrical charge determines movement

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11
Q

Which fragment travel further and faster?

A

the smaller DNA fragments travel faster and farther in the gel.

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12
Q

which way does DNA run to?

A

THe positive end as DNA is negatively charged

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13
Q

How are fragments separated?

A

in bands

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14
Q

What is a ladder?

A

It sets the fragment size standard

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15
Q

How are samples loaded into the gel?

A

through the use of wells and the current applied over top of the gel

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16
Q

How many controls are there?

A

2, and positive and a negative

17
Q

WHat is the purpose of the negative control

A

to ensure you performed the lab correctly as there should not be any bands in the negative control

18
Q
A