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Manipulating DNA
Author :
Tre Briercliffe
1.
DNA is negatively charged
A.
B.
2.
DNA is positively charged
A.
B.
3.
Hydrogen bonds hold DNA strands together
A.
B.
4.
PCR amplifies DNA (makes multiple copies)
A.
B.
5.
electrophoresis amplifies DNA (makes multiple copies)
A.
B.
6.
Sanger Sequencing uses fluorescent tags
A.
B.
7.
In PCR the temperature needs to be raised to allow the primers to anneal
A.
B.
8.
Restriction enzymes cut DNA into equal sized pieces
A.
B.
9.
Sanger sequencing uses a mix of normal and terminator nucleotides
A.
B.
10.
Sanger sequencing uses elements of PCR and electrophoresis
A.
B.
11.
DNA is separated by size in electrophoresis
A.
B.
12.
The enzyme used in PCR is RNA polymerase
A.
B.