chapter work Flashcards

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1
Q

Gel electrophorisis

A

separates DNA fragments by size, using electric currents, to compare to other DNA

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2
Q

Polymerase Chain reaction

A

replicates DNA in 3 steps. Denaturation, Annealing and Elongation

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3
Q

Denaturation

A

part of PCR heat DNA to 94 degrees so the hydrogen bonds brake separating the DNA into 2 strands

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4
Q

annealing

A

Part of PCR reduces temperature to 55 degrees so the primers can attach

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5
Q

Elongation

A

part of PCR temperature increase to 72 degrees so the Taq polimerase works at it ideal temp so it most efficient

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6
Q

what you need for PCR

A
  1. DNA
  2. Primers
  3. Necleotides
  4. Taq polimerase
  5. mix buffer
  6. PCR tube
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7
Q

What charge is DNA

A

Negative (-)

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8
Q

what charge does DNA move to

A

positive terminal

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9
Q

what “glues” the DNA backbone together after it has been cut

A

Ligases

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10
Q

whats responsible for “cutting” DNA

A

restriction enzymes

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11
Q

standard ladder

A

use in gel electrophoresis to compare to the unknown sample

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12
Q

polimerse

A

add complimentry nucleotides to a sequence.

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13
Q

CRISPR cas-9 in Bacteria

A

Cause viral DNA to become non functioning

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14
Q

CRISPR Cas-9 in genetic engineering

A

causes a chosen gene thats already been created to go in the cut site

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15
Q

cleaves

A

CRISPER Cas-9 cuts DNA

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16
Q

Exposure

A

bacteria is exposed to viral DNA it takes a sample of the DNA and put it in the PAM sequence.

17
Q

Expression

A

cas-9 and guide RNA (from PAM sequence) combine making a CRISPR cas-9 complex, which scan the DNA for a complimentary to gRNA

18
Q

Extermination

A

If complimentry bases to guide RNA are found the cas-9 cleaves (cuts) it and random necleotides make the viral DNA non-functional

19
Q

what type or RNA is in a CRISPR Cas-9 complex?

A

guide RNA, gRNA