Worksheets1.3 HBS
Total questions: 48
Worksheet time: 33mins
This laboratory procedure is known as
CLONING
gel electrophoresis
chromatography
use of a dichotomous key
In preparation for an electrophoresis procedure, enzymes are added to DNA in order to
convert the DNA into gel
cut the DNA into fragments
change the color of the DNA
produce longer sections of DNA
A student performed a gel electrophoresis experiment. The results are represented in the diagram
below. Compared to the fragments at the top of the gel, the fragments at the lower end are
larger, and move slower
larger, and move faster
smaller, and move faster
smaller, and move slower
This technique used to analyze DNA involves the
synthesis of new DNA strands from subunits
separation of DNA fragments based on size
production of genetically engineered DNA molecules
removal of defective genes from DNA
micropipette
transfer pipette
pipette pump
serological pipette
Micropipettes are very accurate tools of measurement, but they are only as accurate as the person using it.
true
false
Always change out the micropipette tip when changing reagents.
true
false
This is a p20 micropipette.
How many microliters will this micropipette take up?
500 uL
50 uL
5.0 uL
0.5 uL
This is a p200 micropipette.
How many microliters will this micropipette take up?
500 uL
50 uL
5.0 uL
0.5 uL
What is the denaturation step?
mutating RNA polymerase
Cooling DNA to allow primers to form
separating DNA helix in a cold environment
separating DNA helix with using heat
What happens after you have denatured your DNA?
It denatures again.
Primers attach to the gene of interest.
The gene elongates
PCR is over
Who commited the crime?
Suspect 1
Suspect 2
Suspect 3
Who is the father?
Man 1
Man 2
Man 3
Who is the father?
Dad 1
Dad 2
Dad 3
How are buffers used in Electrophoresis?
Conduct electricity
Remove salts
Add extension energy
Dissolve excess DNA
1. If the recognition sequence of the restriction enzyme HindIII is AAGCTT, then how many covalent bonds will be broken by the enzyme in the following DNA molecule?
1
2
3
4
1. The DNA base sequences recognized by Endonuclease are called
a).Restriction Site
b). Recognition Site
c).Fragmentation Site
d).cutting Site
How do we name restriction Enzymes ?
a).First letter in Cap for Genus, next two letter in small for species, next one letter for strain and roman numeral for order of discovery
b). First two letter in Cap for Genus, next one letter in small for species, next one letter for strain and English numeral for order of discovery
c). First two letter in Cap for Genus, next one letter in capital for species, next one letter for strain and roman numeral for order of discovery
d). First two letter in Cap for Genus, next one letter in small for species, next one letter for strain and roman numeral for order of discovery
The recognition sites for restriction enzymes are :
a).Tautomer
b). Pallindrome
c).Metamere
d).Acronym
Restriction Enzymes are isolated from :
a).Protozoa
b). Bacteria
c).Virus
d).Fungi
Restriction Enzymes were primarily used as :
a).Defence by Protozoa against antibiotics
b).Tool by Virus to cleave Bacterial genome
c)Defence by Bacteria against bacteriophages viruses
d).All of the above
How many RFLPs (fragements) would form if the following DNA was cut by HaeIII. The restriction site for HaeII GG^CC.
1
2
3
4
How long is the shortest RFLP when DNA was cut by HaeIII. The restriction site for HaeII GG^CC.
14
18
6
4
The enzyme EcoRI cuts at GAATTC. How many RFLPS will form?
1
2
3
4
When the following bacterial plasmid DNA is cut with a restriction enzyme, how many bands will appear on the gel?
1
2
3
4
