

DNA technology
Presentation
•
Biology
•
12th Grade
•
Practice Problem
•
Easy
Sara Alattar
Used 4+ times
FREE Resource
16 Slides • 24 Questions
1
DNA Technology
2
• An organism’s genome is the total DNA present in the nucleus of
each cell.
• The gene is considered the basic unit of inheritance.
• Genes are passed from parents to offspring and contain the
information needed to specify physical and biological traits
Introduction: The Role of DNA
Explain the impact of genetic engineering on the function and significance of DNA
3
Multiple Choice
The ______________ is considered the basic unit of inheritance.
4
Multiple Choice
An organism’s__________ is the total DNA present in the nucleus of each cell.
5
Multiple Choice
____________ contain the information needed to specify physical and biological traits
6
The Role of DNA
DNA replication
7
Multiple Choice
Cells use instructions from DNA to produce enzymes that make the purple pigment, this is an example of DNA__________
Expression
copying
storage
8
Multiple Choice
DNA can make copies of itself is known as __________
9
Multiple Choice
DNA can replicate but it cannot store any information.
10
Central Dogma of Molecular Biology
In the cells, information flows from DNA to RNA to proteins.
11
Multiple Choice
What is the Central Dogma of molecular biology?
DNA replication, transcription, and translation
The process of protein folding.
12
In order to study DNA, various tools are implemented to
copy and separate different DNA fragments:
• Gel Electrophoresis
Used to separate DNA fragments
• Polymerase Chain Reaction (PCR)
Used to copy DNA fragments
DNA Tools
13
Multiple Choice
Gel Electrophoresis is used to ___________
14
Multiple Choice
Polymerase Chain Reaction (PCR) is used to _________
copy DNA fragments and amplify it
15
Gel Electrophoresis
•In gel electrophoresis, an electric current is
used to separate DNA fragments according to
the size of the fragments.
DNA Tools: Electrophoresis
16
Multiple Choice
In gel electrophoresis, an electric current is used to separate DNA fragments according to the___________ of the fragments.
17
Gel Electrophoresis
• DNA is a negatively charged molecule
• When an electric current is
applied, the DNA fragments
move toward the positive
end of the gel.
DNA Tools: Electrophoresis
Describe the methodologies of PCR, Gel electrophoresis, and DNA sequencing
18
Multiple Choice
DNA is a __________ charged molecule
19
Multiple Choice
In gel electrophoresis technique, the gel is ____________ charged
20
Gel Electrophoresis
•The unique pattern created
based on the size of the DNA
fragments can be compared to
known DNA fragments for
identification.
DNA Tools: Electrophoresis
Describe the methodologies of PCR, Gel electrophoresis, and DNA sequencing
21
Multiple Choice
In_________________ the unique pattern created based on the size of the DNA fragments can be compared to known DNA fragments for identification.
Gel Electrophoresis
22
DNA Tools:
Electrophoresis
1- Adding the DNA samples into the gel
2-Running the samples
4- Results obtained: DNA
Bands can be identified
3- The DNA fragments will migrate
and then separate
23
1000 bp
700 bp
600 bp
500 bp
400 bp
300 bp
200 bp
100 bp
800 bp
900 bp
Larger
Fragments
Smaller
Fragments
DNA Samples are
separated based on size.
The smaller fragments
travel farther than the
larger fragments.
The size of the band
indicates how many DNA
fragments exist at that
size.
For example:
More Fragments
Less Fragments
Sample
1
Sample
2
Sample
3
DNA
Ladder
DNA Tools: Electrophoresis
24
Multiple Choice
In gel electrophoresis, the smaller fragments travel__________ than the larger fragments.
25
Multiple Choice
In gel electrophoresis, the size of the band indicates __________
weight of each band
electric charge of the fragments
how many DNA fragments exist at that size.
26
Gel electrophoresis is a method for separating and analyzing DNA fragments. The molecules are
separated based on size and charge
Gel Electrophoresis can be used to get DNA fingerprints for crime scenes/Forensics.
Gel Electrophoresis can be used to determine evolutionary relatedness.
Electrophoresis Uses
27
Open Ended
What applications can gel electrophoresis be used for?
28
DNA Tools: PCR
Polymerase Chain Reaction
•technique that is used to make millions of
copies of a specific region of a DNA fragment.
•PCR can copy or amplify a single DNA molecule
numerous times for use in analysis.
29
Open Ended
What is the purpose of the PCR?
30
Components of PCR
Nucleotides: Basic units of DNA, consisting of adenine (A), cytosine (C), guanine (G), and thymine (T), which are assembled during the amplification process to build the new DNA strands.
PCR machine: Instrument that performs
the PCR reaction.
31
Multiple Select
What are the four types of DNA nucleotides? choose four answers
Adenine (A)
Thymine (T)
Guanine (G)
Cytosine (C)
Uracil(U)
32
Components of PCR
Primers: Specific molecules that target and identify the DNA sequence to be amplified, starting the amplification process.
Polymerase: Enzyme responsible for replicating and amplifying the DNA sequence targeted by the primers.
33
Multiple Choice
______________ Specific molecules that target and identify the DNA sequence to be amplified
34
Multiple Choice
DNA______________Enzyme responsible for replicating and amplifying the DNA sequence targeted by the primers.
Polymerase
35
DNA Tools: PCR
• PCR is a biological version of a copy machine.
• During each PCR cycle, the reaction mixture is heated to separate the DNA strands and then cooled to allow primers to bind to
complementary sequences.
• The DNA polymerase then adds nucleotides to form new DNA molecules.
36
1. DNA is heated to
separate strands.
2. The mixture is cooled and
primers bind to the strands.
3. DNA polymerase
adds nucleotides to
strands, producing
two complementary
strands.
4. The process repeats and the
section of DNA is copied again.
Each cycle doubles the amount
of DNA.
DNA Tools: PCR
37
Multiple Choice
First step of PCR is________
DNA polymerase
adds nucleotides to
strands, producing
two complementary
strands.
DNA is heated to
separate strands.
The mixture is cooled and
primers bind to the strands.
The process repeats and the
section of DNA is copied again.
Each cycle doubles the amount
of DNA.
38
Multiple Choice
3rd step of PCR is________
DNA polymerase
adds nucleotides to
strands, producing
two complementary
strands.
DNA is heated to
separate strands.
The mixture is cooled and
primers bind to the strands.
The process repeats and the
section of DNA is copied again.
Each cycle doubles the amount
of DNA.
39
Multiple Choice
2nd step of PCR is________
DNA polymerase
adds nucleotides to
strands, producing
two complementary
strands.
DNA is heated to
separate strands.
The mixture is cooled and
primers bind to the strands.
The process repeats and the
section of DNA is copied again.
Each cycle doubles the amount
of DNA.
40
Multiple Choice
4th step of PCR is________
DNA polymerase
adds nucleotides to
strands, producing
two complementary
strands.
DNA is heated to
separate strands.
The mixture is cooled and
primers bind to the strands.
The process repeats and the
section of DNA is copied again.
Each cycle doubles the amount
of DNA.
DNA Technology
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