1 |
Course Title: |
MOLECULAR BIOLOGY TECHNIQUES |
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Course Code: |
MBG2006 |
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Type of Course: |
Compulsory |
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Level of Course: |
First Cycle |
5 |
Year of Study: |
2 |
6 |
Semester: |
4 |
7 |
ECTS Credits Allocated: |
6 |
8 |
Theoretical (hour/week): |
2 |
9 |
Practice (hour/week) : |
2 |
10 |
Laboratory (hour/week) : |
0 |
11 |
Prerequisites: |
None |
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Recommended optional programme components: |
None |
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Language: |
Turkish |
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Mode of Delivery: |
Face to face |
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Course Coordinator: |
Dr. Ögr. Üyesi ELİF UZ |
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Course Lecturers: |
Araştırma Görevlileri |
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Contactinformation of the Course Coordinator: |
Dr. Öğr. Üyesi Elif UZ YILDIRIM Bursa Uludağ Üniversitesi Fen-Edebiyat Fak., Moleküler Biyoloji ve Genetik Bölümü elifuz@uludag.edu.tr 902242941776 |
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Website: |
|
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Objective of the Course: |
To comprehend the basic logic of the techniques used in molecular biology and genetics studies. |
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Contribution of the Course to Professional Development |
To gain the capacity of choosing the right method during experimental studies. Moreover, to choose the right techiques, since the students learn the similarities and differences among methods. |
Week |
Theoretical |
Practical |
1 |
Basic concepts of techniques used in molecular biology: A general overview I |
Laboratory rules and safety (Groups A1-B1) |
2 |
Basic concepts of techniques used in molecular biology: A general overview II |
Laboratory rules and safety (Groups A2-B2) |
3 |
Isolation techniques (DNA, RNA and protein) |
Laboratory equipments (Groups A1-B1) |
4 |
cDNA synthesis, library preparation |
Laboratory equipments (Groups A2-B2) |
5 |
Conepts of PCR |
Laboratory consumables (Groups A1-B1) |
6 |
Types of PCR and concepts of RT-PCR |
Laboratory consumables (Groups A2-B2) |
7 |
Electrophoretic techniques (Agarose and PAGE) |
Solution Preparation (Groups A1-B1) |
8 |
Principles of hybridization techniques (Southern and Northern blot) |
Solution Preparation (Groups A2-B2) |
9 |
Principles of hybridization techniques (Western blot) |
DNA Isolation (Groups A1-B1) |
10 |
DNA sequencing techniques |
DNA Isolation (Groups A2-B2) |
11 |
siRNA/miRNA, Microarray |
Spectrophotometric measurements of DNA and Agarose Gel (Groups A1-B1) |
12 |
Genome editing using nucleases (ZFNs, TALENs and CRISPR-Cas) |
Spectrophotometric measurements of DNA and Agarose Gel (Groups A2-B2) |
13 |
ChIP, ELISA, protein sequencing |
PCR and gel electrophoresis (Groups A1-B1) |
14 |
Yeast complementation: Yeast one hybrid, yeast two hybrid and yeast three hybrid |
PCR and gel electrophoresis (Groups A2-B2) |