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Curricular information is subject to change
On completion of this module, students are expected to be able to:
1. Describe the basic principles of gene transcription and PCR-based analysis of gene expression. These include, but are not limited to, the following:
a. Regulation of gene expression
i. Gene promoters and enhancers
ii. Transcription start sites
iii. Transcription factors and polymerase recruitment
iv. RNA splicing
b. Methods for assessing gene expression
i. End point PCR
ii. Sybr green based QPCR
iii. Taqman based QPCR
c. RNA isolation
i. Cultured cells vs Tissues
ii. RNA stability
iii. RNA quantification
d. cDNA synthesis
i. Selection of reverse transcriptase and primers
e. Design of gene-specific primers
f. Normalisation of QPCR data
i. Selecting suitable “House keeping” genes
2. Demonstrate laboratory competence in performing tasks relating to Learning Outcome 1.
Student Effort Type | Hours |
---|---|
Tutorial | 12 |
Laboratories | 60 |
Autonomous Student Learning | 40 |
Total | 112 |
Not applicable to this module.
Remediation Type | Remediation Timing |
---|---|
Repeat | Within Two Trimesters |
• Feedback individually to students, post-assessment
Feedback will be provided on graded laboratory reports.