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Module Specifications.

Current Academic Year 2024 - 2025

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Date posted: September 2024

Module Title Gene Cloning, Protein Expression & Purification
Module Code BE380 (ITS) / GCB1012 (Banner)
Faculty Science & Health School Biotechnology
Module Co-ordinatorJiafu Wang
Module TeachersDenise Harold, Emma Finlay, Paul Cahill, Paula Meleady
NFQ level 8 Credit Rating 5
Pre-requisite Not Available
Co-requisite Not Available
Compatibles Not Available
Incompatibles Not Available
Repeat the module
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Description

To introduce students to applications of Web based bioinformatic analyses To train students in the basic practical techniques of recombinant DNA technology and to develop their understanding of strategies used in the construction, mapping and expression and purification of recombinant molecules.

Learning Outcomes

1. Apply computational skills to analyse DNA sequences using bioinformatics tools
2. Construct recombinant DNA molecules using the techniques of gene cloning
3. Analyse DNA structure and gene expression using restriction digestion and phenotypic detection
4. Purify a recombinant protein using affinity chromatography
5. Record laboratory research results through the maintenance of a laboratory notebook, accurately reporting experimental results and conclusions.
6. Effectively engage in safe laboratory practices, encompassing proper conduct, attire, risk mitigation, and disposal procedures.



Workload Full-time hours per semester
Type Hours Description
Laboratory36Molecular Biology Laboratory
Independent Study71Preparation before lab, data analysis, literature review, and studying.
Directed learning18Laboratory report preparation
Total Workload: 125

All module information is indicative and subject to change. For further information,students are advised to refer to the University's Marks and Standards and Programme Specific Regulations at: http://www.dcu.ie/registry/examinations/index.shtml

Indicative Content and Learning Activities

Overview
Overview of bioinformatics and nucleotide and protein databases. Derivation and format of nucleotide and protein sequences e.g. FASTA. Using web resources e.g. NCBI to access and retrieve sequences. Comparing DNA and protein sequences with appropriate databases using BLAST. Displaying similarities using alignments and multiple alignmentsIdentification of coding regions and consensus sequences. Translating nucleotide sequences and searching for open reading frames. Analysis of nucleotide sequences for restriction enzyme sites. Primer design for the PCR. Application of PCR for the amplification of target genes. Analysis of DNA by agarose gel electrophoresis. DNA restriction and restriction mappingCloning in plasmid vectorsLigation. Transformation and electroporation. Extraction of plasmid DNA from transformants and its analysis by restriction and gel electrophoresis. Site directed mutagenesis. Purification of a recombinant protein using a one step affinity chromatography.

Assessment Breakdown
Continuous Assessment100% Examination Weight0%
Course Work Breakdown
TypeDescription% of totalAssessment Date
AssignmentBioinformatics tasks.20%n/a
In Class TestInclude questions on bioinformatics and the recombinant DNA practical.30%n/a
Report(s)Laboratory reports50%n/a
Reassessment Requirement Type
Resit arrangements are explained by the following categories:
Resit category 1: A resit is available for both* components of the module.
Resit category 2: No resit is available for a 100% continuous assessment module.
Resit category 3: No resit is available for the continuous assessment component where there is a continuous assessment and examination element.
* ‘Both’ is used in the context of the module having a Continuous Assessment/Examination split; where the module is 100% continuous assessment, there will also be a resit of the assessment
This module is category 2
Indicative Reading List

    Other Resources

    None

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