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GRADUATE INSTITUTE of HEALTH SCIENCES / DEPARTMENT of MEDICAL BIOLOGY
Doctorate
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SABE
GRADUATE INSTITUTE of HEALTH SCIENCES / DEPARTMENT of MEDICAL BIOLOGY / Doctorate
Katalog Ana Sayfa
  Katalog Ana Sayfa  KTÜ Ana Sayfa   Katalog Ana Sayfa
 
 

TBI 625Recombinant DNA Technology2+0+2ECTS:7.5
Year / SemesterFall Semester
Level of CourseThird Cycle
Status Compulsory
DepartmentDEPARTMENT of MEDICAL BIOLOGY
Prerequisites and co-requisitesNone
Mode of DeliveryFace to face, Group study
Contact Hours14 weeks - 2 hours of lectures and 2 hours of laboratory per week
Lecturer--
Co-Lecturer
Language of instructionTurkish
Professional practise ( internship ) None
 
The aim of the course:
Aim of this course is; understanding the theory and applications of recombinant DNA technology by students.
 
Programme OutcomesCTPOTOA
Upon successful completion of the course, the students will be able to :
PO - 1 : Student defines biochemical reagents used in recombinant DNA technology.
PO - 2 : Student defines vectors used in recombinant DNA technology and can compare them.
PO - 3 : Student knows in vitro and in vivo cloning
PO - 4 : Student explains different cloning methods
PO - 5 : Student knows the theory of techniques to change, over express, knock-down and knock-out genes
PO - 6 : Student knows about the theory of techniques used in DNA and RNA quantitation.
PO - 7 : Student knows about the theory of approaches used for protein expression, purification and interaction.
PO - 8 : Student has a general idea about the computer programmes used in recombinant DNA technology
PO - 9 : Student defines area of usage of recombinant DNA technology
CTPO : Contribution to programme outcomes, TOA :Type of assessment (1: written exam, 2: Oral exam, 3: Homework assignment, 4: Laboratory exercise/exam, 5: Seminar / presentation, 6: Term paper), PO : Learning Outcome

 
Contents of the Course
This course contains the topics such as; introduction to gene manipulation, biochemical reagents used for manipulation of DNA molecules (restriction enzymes, ligases, phosphotases ..etc.), and their functions, biology of vectors used in cloning (plasmid, cosmid, phasmid ..etc.), gen cloning strategies, model organisms applied for cloning, transformation and transfection of vectors into host organisms, site directed mutagenesis, quantitation of mRNA (REAL Time PCR), gene knock-out and knock-down strategies, protein expression and purification approaches, protein interactions methods, bioinformatics, applications of recombinant DNA technology.
 
Course Syllabus
 WeekSubjectRelated Notes / Files
 Week 1Introduction to Recombinant DNA Technology
 Week 2Biochemical reagents used for manipulation of DNA molecules and their functions.
 Week 3Biology of vectors used in cloning and their applications.
 Week 4Model organisms used in recombinant DNA technology and their comparisons.
 Week 5Gene cloning Strategies
 Week 6DNA Transfection and transformation methods for model organisms.
 Week 7Site-Directed Mutagenesis, gene knock-down and knock-out strategies
 Week 8Midterm
 Week 9Gene quantitation methods
 Week 10Protein expression and purification approaches
 Week 11Approaches to analyse protein interactions
 Week 12Bioinformatics
 Week 13Common use areas of recombinant DNA technology
 Week 14Student presentations
 Week 15Student presentations
 Week 16Endf of Term exam
 
Textbook / Material
1S.B. Primrose ve R.M. Twyman, Principles of Gene Manipulation and Genomics,Blackwell yayınevi,2006,1-4051-3544-1
 
Recommended Reading
 
Method of Assessment
Type of assessmentWeek NoDate

Duration (hours)Weight (%)
Mid-term exam 1 2 30
Presentation 1 1 20
Homework/Assignment/Term-paper 1 1 10
End-of-term exam 1 2 40
 
Student Work Load and its Distribution
Type of workDuration (hours pw)

No of weeks / Number of activity

Hours in total per term
Yüz yüze eğitim 3 12 36
Sınıf dışı çalışma 3 3 9
Arasınav için hazırlık 4 5 20
Arasınav 1 2 2
Ödev 5 2 10
Dönem sonu sınavı için hazırlık 4 5 20
Dönem sonu sınavı 1 2 2
Diğer 1 5 2 10
Total work load109