Abstract
Type 1 Diabetes Mellitus is a condition in which the p cells that produce insulin undergo autoimmune destruction. It is associated with susceptibility gene of HLA region as well as non-MHC loci for example CTLA4 gene. NG transition at position 49 of exon 1 of the CTLA4 gene results in threonine to alanine substitution and was reported to have association with Type 1 Diabetes Mellitus. Objective of this study is to develop genotyping method for polymorphism detection of CTLA4 gene with Type 1 Diabetes Mellitus. Primers were designed and conditions for PCR were manipulated to obtain the most optimized PCR condition. 151 PCR was run at annealing temperature of 55°C and the intensity of the bands is higher as compared to annealing temperature of 58°C. Both wild type and mutant type bands appeared at different densities during the 2°d PCR analysis for all the five samples. More studies on association of CTLA4 gene with Type 1 Diabetes Mellitus are needed especially on Malaysian population as early detection is able to slow down or even stop disease progression and hence improve their quality of life.
Metadata
Item Type: | Thesis (Degree) |
---|---|
Creators: | Creators Email / ID Num. Rosu, Soraya UNSPECIFIED |
Contributors: | Contribution Name Email / ID Num. Thesis advisor Fauzi, Hamid UNSPECIFIED |
Subjects: | R Medicine > RC Internal Medicine > Diabetes Mellitus R Medicine > RS Pharmacy and materia medica > Pharmacopoeias |
Divisions: | Universiti Teknologi MARA, Selangor > Puncak Alam Campus > Faculty of Pharmacy |
Programme: | Bachelor of Pharmacy |
Keywords: | PCR method, polymorphism of cytotoxic t-lymphocyte-associated protein 4 (CTLA4), type 1 diabetes mellitus (TIDM) |
Date: | 2014 |
URI: | https://ir.uitm.edu.my/id/eprint/111122 |
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