Molecular Biology Techniques

Descripción

Test sobre Molecular Biology Techniques , creado por MPusey el 29/12/2014.
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Resumen del Recurso

Pregunta 1

Pregunta
What monomer units make up the DNA molecule?
Respuesta
  • Nucleotides
  • Monosaccharides
  • Amino acids
  • Phospholipids

Pregunta 2

Pregunta
Which of the four nucleotide bases are purine bases?
Respuesta
  • Adenine
  • Guanine
  • Cytosine
  • Thymine

Pregunta 3

Pregunta
How many carbon rings do purine bases have?
Respuesta
  • One
  • Two

Pregunta 4

Pregunta
Which of the four bases are pyramidine bases?
Respuesta
  • Adenine
  • Guanine
  • Cytosine
  • Thymine

Pregunta 5

Pregunta
How many carbon rings do pyramidine bases have?
Respuesta
  • One
  • Two

Pregunta 6

Pregunta
In which direction do the nucleotide chains run in?
Respuesta
  • 5' to 3'
  • 3' to 5'

Pregunta 7

Pregunta
What type of sequences do restriction enzymes recognize?
Respuesta
  • Palindromic sequences
  • Repetitive sequences
  • Sequences that only occur once in the whole of our genome

Pregunta 8

Pregunta
All restriction enzymes recognize the same sequence. True or false?
Respuesta
  • True
  • False

Pregunta 9

Pregunta
Restriction enzymes that cut in the middle of the palindrome leave....
Respuesta
  • Blunt ends
  • Sticky ends

Pregunta 10

Pregunta
Restriction enzymes that cut at the end of the palindrome leave......
Respuesta
  • Sticky ends
  • Blunt ends

Pregunta 11

Pregunta
What enzyme could be considered the opposite to a restriction enzyme?
Respuesta
  • RNA polymerase
  • DNA ligase
  • DNA polymerase

Pregunta 12

Pregunta
How do restriction enzymes cut DNA?
Respuesta
  • They hydrolyse the phosphdiester backbone
  • They perform a condensation reaction on the phosphodiester backbone
  • They hydrolyse the hydrogen bonds between DNA bases

Pregunta 13

Pregunta
What type of bonds does DNA ligase form in DNA?
Respuesta
  • Phosphodiester bonds
  • Hydrogen bonds
  • Peptide bonds
  • Triple carbon bonds

Pregunta 14

Pregunta
What is the main piece of equipment required for gel electrophoresis?
Respuesta
  • Agrose gel plate
  • Test tube
  • Restriction enzyme
  • DNA primers
  • Free nucleotides

Pregunta 15

Pregunta
What is gel electrophoresis used for?
Respuesta
  • To determine the size of DNA fragments
  • To map out plasmids
  • To replicate large amounts of DNA

Pregunta 16

Pregunta
Are DNA fragments positively or negatively charged?
Respuesta
  • Positively
  • Negatively

Pregunta 17

Pregunta
Which end of the agrose gel plate will the DNA samples move towards?
Respuesta
  • The positive end
  • The negative end

Pregunta 18

Pregunta
Which fragments will move further during gel electrophoresis?
Respuesta
  • Smaller ones
  • Larger ones

Pregunta 19

Pregunta
What are restriction maps used for?
Respuesta
  • To map out plasmids
  • To determine the size of fragments of DNA
  • To replicate large amounts of DNA
  • To discover new restriction enzymes
  • To isolate restriction enzymes for later use

Pregunta 20

Pregunta
If a restriction enzyme cuts a plasmid in one place only, how many fragments of the plasmid will there be in total?
Respuesta
  • One
  • Two
  • Three
  • Not enough information

Pregunta 21

Pregunta
If a restriction enzyme cuts a plasmid in two places only, how many plasmid fragments will there be?
Respuesta
  • One
  • Two
  • Three
  • Not enough information

Pregunta 22

Pregunta
What is Polyermerase Chain Reaction (PCR) used for?
Respuesta
  • Replicating known sequences of DNA
  • Replicating unknown sequences of DNA
  • Mapping out DNA sequence on a plasmid
  • Cutting DNA at a particular sequence

Pregunta 23

Pregunta
What is missing from this list of what is required to complete PCR? Template, 2 primers, free nucleotides, buffer.
Respuesta
  • DNA polymerase
  • RNA polymerase
  • More primers
  • DNA ligase

Pregunta 24

Pregunta
What are the three stages of PCR?
Respuesta
  • Denaturation
  • Annealing
  • Extension
  • Replication
  • Repetition

Pregunta 25

Pregunta
What temperature should denauration take place at in PCR?
Respuesta
  • 95 degrees
  • 50-65 degrees
  • 72 degrees

Pregunta 26

Pregunta
At what temperature should the annealing stage of PCR take place at?
Respuesta
  • 95 degrees
  • 50-65 degrees
  • 72 degrees

Pregunta 27

Pregunta
At what temperature should the extension stage of PCR taken place at?
Respuesta
  • 90 degrees
  • 50-65 degrees
  • 72 degrees

Pregunta 28

Pregunta
If there were four strands of DNA in the PCR before one cycle, how many would there be after the cycle has completed?
Respuesta
  • Four
  • Eight
  • Sixteen

Pregunta 29

Pregunta
What is the purpose of the denaturation stage of PCR?
Respuesta
  • To separate the strands of DNA
  • To damage the DNA so that it cannot replicate as it would do in the cell
  • To heat the DNA until it is no longer able to code for specific proteins

Pregunta 30

Pregunta
What enzyme extends the DNA strand during the extension phase of PCR?
Respuesta
  • DNA polymerase
  • RNA polymerase
  • DNA ligase

Pregunta 31

Pregunta
When would you use cloning instead of PCR to replicate DNA?
Respuesta
  • When there are more than 1000 base pairs in the sequence
  • When the base sequence is unknown
  • When the base sequence in known
  • When the base sequence contains too many repetitions

Pregunta 32

Pregunta
Why is E. coli often used in the cloning process?
Respuesta
  • Because it grows rapidly in cheap material
  • Because it is the easiest bacteria to make safe for human use
  • Because it is easy to extract the DNA from
  • Because it is easy to re-insert the plasmid into
  • Because it is a very common bacteria
  • Because it has no cell membranes
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