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Basics of genetic engineering and diagnosticsLaajuus (5 cr)

Code: 5021169

Credits

5 op

Objective

The participants are able to describe the essentials of diagnostics and basic concepts and methods of diagnostics and genetic engineering. The participants know the basic principles and methods of genetic engineering.

Content

- basics and basic techniques of genetic engineering

- essentials, concepts and methods of diagnostics

Enrollment

02.12.2024 - 13.01.2025

Timing

13.01.2025 - 09.03.2025

Number of ECTS credits allocated

5 op

Mode of delivery

Contact teaching

Campus

Lemminkäisenkatu

Teaching languages
  • Finnish
  • English
Seats

10 - 25

Degree programmes
  • Degree Programme in Biotechnology and Chemical Engineering
Teachers
  • Jani Pelkonen
Groups
  • PBIOKES22Bio
    PBIOKES22Bio
  • PBIOKES22

Objective

The participants are able to describe the essentials of diagnostics and basic concepts and methods of diagnostics and genetic engineering. The participants know the basic principles and methods of genetic engineering.

Content

- basics and basic techniques of genetic engineering

- essentials, concepts and methods of diagnostics

Materials

Suominen I., Pärssinen, R., Haajanen, K. ja Pelkonen, J. Geenitekniikka (finnish)
Brown: Gene Cloning & DNA Analysis (english)
Lecture notes on Its-platform

Teaching methods

Group and individual assignments
Laboratory experiments, Lab reports

Exam schedules

Will be updated beginning of the course

International connections

Flipped learning, Contact teaching

Completion alternatives

Conducting research in a research group. For further information contact Jani Pelkonen (jani.pelkonen@turkuamk.fi).

Student workload

Theoretical part:
Lectures, presentations, assignments and self-studying (approx. 78 h)

Laboratory experiments:
24 h laboratory works (3 weeks, 8 h / week)
29 h self-studying and reporting of laboratory works

Content scheduling

The student should understand the essential principles of genetic engineering and diagnostic practices, and know the basic terminology and methods. The course consist of theoretical part (3 cr) and laboratory woks (2 cr).

Spesific topics include:

-Nucleic acids & molecular biology
-Requirements of gene technology, Isolation and analysis of nucleic acids
-Cloning vectors, Regulation of gene activity, expression, autoinduction
-Nucleic acids modifying enzymes. Ligation., Introducing DNA into host cells, PCR
-DNA sequencing, Antibodies, basics of immunology
-Immunoassays
-Immunodiagnostics

Laboratory works:
* Amplification of egfp gene by PCR
* Restriction enzymes and agarose gel electrophoresis
* Gel extraction of the DNA from agarose gel electrophoresis
* Cloning of PCR amplified DNA fragment and transformation
* Characterization of transformants

Evaluation scale

H-5

Assessment methods and criteria

The course consist of theory part and laboratory part. The theory part and its tasks emphasis 60% and labworking and reporting emphasis 40% of the final grade.
The course grading is composed of four tasks and each of them need to be approved:
* Group presentation task, max. 3 points (teacher + peer evaluation)
* Reflection report (individual), max. 4 points
* Multiple choice task (individual), max. 3 points
* Laboratory report as a presentation/video, max 5 points
Total points are converted to course grade:
<5p=0, 5-6p=1, 7-8p=2, 9-11p=3, 12-13p=4, 14-15p=5

Enrollment

01.12.2023 - 15.01.2024

Timing

15.01.2024 - 08.03.2024

Number of ECTS credits allocated

5 op

Mode of delivery

Contact teaching

Campus

Lemminkäisenkatu

Teaching languages
  • English
Degree programmes
  • Degree Programme in Biotechnology and Chemical Engineering
Teachers
  • Jani Pelkonen
Groups
  • PBIOKES21
  • PBIOKES21Bio
    PBIOKES21Bio

Objective

The participants are able to describe the essentials of diagnostics and basic concepts and methods of diagnostics and genetic engineering. The participants know the basic principles and methods of genetic engineering.

Content

- basics and basic techniques of genetic engineering

- essentials, concepts and methods of diagnostics

Materials

Suominen I., Pärssinen, R., Haajanen, K. ja Pelkonen, J. Geenitekniikka (finnish)
Brown: Gene Cloning & DNA Analysis (english)
Lecture notes on Its-platform

Teaching methods

Group and individual assignments
Laboratory experiments, Lab reports

Exam schedules

will be updated beginning of the course

International connections

Flipped learning, Contact teaching

Completion alternatives

Conducting research in a research group. For further information contact Jani Pelkonen (jani.pelkonen@turkuamk.fi).

Student workload

Theoretical part:
Lectures, presentations, assignments and self-studying (approx. 78 h)

Laboratory experiments:
24 h laboratory works (3 weeks, 8 h / week)
29 h self-studying and reporting of laboratory works

Content scheduling

The student should understand the essential principles of genetic engineering and diagnostic practices, and know the basic terminology and methods. The course consist of theoretical part (3 cr) and laboratory woks (2 cr).

Spesific topics include:

-Nucleic acids & molecular biology
-Requirements of gene technology, Isolation and analysis of nucleic acids
-Cloning vectors, Regulation of gene activity, expression, autoinduction
-Nucleic acids modifying enzymes. Ligation., Introducing DNA into host cells, PCR
-DNA sequencing, Antibodies, basics of immunology
-Immunoassays
-Immunodiagnostics

Laboratory works:
* Amplification of egfp gene by PCR
* Restriction enzymes and agarose gel electrophoresis
* Gel extraction of the DNA from agarose gel electrophoresis
* Cloning of PCR amplified DNA fragment and transformation
* Characterization of transformants

Evaluation scale

H-5

Assessment methods and criteria

The course consist of theory part and laboratory part. The theory part and its tasks emphasis 60% and labworking and reporting emphasis 40% of the final grade.
The course grading is composed of four tasks and each of them need to be approved:
* Group presentation task, max. 3 points (teacher + peer evaluation)
* Reflection report (individual), max. 4 points
* Multiple choice task (individual), max. 3 points
* Laboratory report as a presentation/video, max 5 points
Total points are converted to course grade:
<5p=0, 5-6p=1, 7-8p=2, 9-11p=3, 12-13p=4, 14-15p=5

Enrollment

10.12.2022 - 15.01.2023

Timing

09.01.2023 - 10.03.2023

Number of ECTS credits allocated

5 op

Mode of delivery

Contact teaching

Unit

Engineering and Business

Campus

Kupittaa Campus

Teaching languages
  • English
Seats

0 - 20

Degree programmes
  • Degree Programme in Biotechnology and Chemical Engineering
Teachers
  • Jani Pelkonen
Groups
  • PBIOKES20
  • PBIOKES20bio
    PBIOKES20bio

Objective

The participants are able to describe the essentials of diagnostics and basic concepts and methods of diagnostics and genetic engineering. The participants know the basic principles and methods of genetic engineering.

Content

- basics and basic techniques of genetic engineering

- essentials, concepts and methods of diagnostics

Materials

Suominen I., Pärssinen, R., Haajanen, K. ja Pelkonen, J. Geenitekniikka (finnish)
Brown: Gene Cloning & DNA Analysis (english)
Lecture notes on Its-platform

Teaching methods

Group and individual assignments
Laboratory experiments, Lab reports

Exam schedules

will be updated beginning of the course

International connections

Flipped learning, Contact teaching

Completion alternatives

Conducting research in a research group. For further information contact Jani Pelkonen (jani.pelkonen@turkuamk.fi).

Student workload

Theoretical part:
Lectures, presentations, assignments and self-studying (approx. 78 h)

Laboratory experiments:
24 h laboratory works (3 weeks, 8 h / week)
29 h self-studying and reporting of laboratory works

Content scheduling

The student should understand the essential principles of genetic engineering and diagnostic practices, and know the basic terminology and methods. The course consist of theoretical part (3 cr) and laboratory woks (2 cr).

Spesific topics include:

-Nucleic acids & molecular biology
-Requirements of gene technology, Isolation and analysis of nucleic acids
-Cloning vectors, Regulation of gene activity, expression, autoinduction
-Nucleic acids modifying enzymes. Ligation., Introducing DNA into host cells, PCR
-DNA sequencing, Antibodies, basics of immunology
-Immuno assays
-Immuno diagnostics

Laboratory works:
* AMPLIFICATION OF EGFP GENE BY PCR
* RESTRICTION ENZYMES AND AGAROSE GEL ELECTROPHORESIS
* GEL EXTRACTION OF THE DNA FROM AGAROSE GEL ELECTROPHORESIS
* CLONING OF PCR AMPLIFIED DNA FRAGMENT AND TRANSFORMATION
* CHARACTERIZATION OF TRANSFORMANTS

Evaluation scale

H-5

Assessment methods and criteria

Theory part (60%) and Laboratory part (40%).

Enrollment

01.12.2021 - 09.01.2022

Timing

13.01.2022 - 24.03.2022

Number of ECTS credits allocated

5 op

Mode of delivery

Contact teaching

Unit

Engineering and Business

Teaching languages
  • Finnish
  • English
Teachers
  • Jani Pelkonen
Groups
  • PBIOKES19
  • PBIOKES19bio
    PBIOKES19bio

Objective

The participants are able to describe the essentials of diagnostics and basic concepts and methods of diagnostics and genetic engineering. The participants know the basic principles and methods of genetic engineering.

Content

- basics and basic techniques of genetic engineering

- essentials, concepts and methods of diagnostics

Materials

Suominen I., Pärssinen, R., Haajanen, K. ja Pelkonen, J. Geenitekniikka (finnish)
Brown: Gene Cloning & DNA Analysis (english)

Teaching methods

Group and individual assignments
Laboratory experiments, Lab reports

Exam schedules

will be updated beginning of the course

International connections

Flipped learning, Contact teaching

Completion alternatives

Conducting research in a research group. For further information contact Mika Jokinen (mika.jokinen@turkuamk.fi).

Student workload

Theoretical part:
Lectures, presentations, assignments and self-studying (approx. 78 h)

Laboratory experiments:
24 h laboratory works (3 weeks, 8 h / week)
29 h self-studying and reporting of laboratory works

Content scheduling

The student should understand the essential principles of genetic engineering and diagnostic practices, and know the basic terminology and methods. The course consist of theoretical part (3 cr) and laboratory woks (2 cr).

Spesific topics include:

-Nucleic acids & molecular biology
-Requirements of gene technology, Isolation and analysis of nucleic acids
-Cloning vectors, Regulation of gene activity, expression, autoinduction
-Nucleic acids modifying enzymes. Ligation., Introducing DNA into host cells, PCR
-DNA sequencing, Antibodies, basics of immunology
-Immuno assays
-Immuno diagnostics

Laboratory works:
week 7: AMPLIFICATION OF EGFP GENE BY PCR
week 7: RESTRICTION ENZYMES AND AGAROSE GEL ELECTROPHORESIS
week 9: GEL EXTRACTION OF THE DNA FROM AGAROSE GEL ELECTROPHORESIS
week 9: CLONING OF PCR AMPLIFIED DNA FRAGMENT AND TRANSFORMATION
week 10: CHARACTERIZATION OF TRANSFORMANTS

Evaluation scale

H-5

Assessment methods and criteria

Theory part (60%) and Laboratory part (40%).