Publication: Genotyping of α-thalassemias by the colorimetric nanogold probes
1
Issued Date
2014-11-01
Resource Type
ISSN
18733492
00098981
00098981
Other identifier(s)
2-s2.0-84907334513
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Clinica Chimica Acta. Vol.437, (2014), 197-202
Suggested Citation
Sirinart Chomean, Nantawan Wangmaung, Pornpimol Sritongkham, Chamras Promptmas, Wanida Ittarat Genotyping of α-thalassemias by the colorimetric nanogold probes. Clinica Chimica Acta. Vol.437, (2014), 197-202. doi:10.1016/j.cca.2014.07.033 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/33210
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Genotyping of α-thalassemias by the colorimetric nanogold probes
Other Contributor(s)
Abstract
Background: The novel colorimetric nanogold probe was created to genotype subgroups of the mostly found α-thalassemias. They are α-thalassemia 1 (SEA and THAI deletion) and α-thalassemia 2 (3.7-kb and 4.2-kb deletion). Methods: The genotyping was performed by two-steps hybridizations. First step was hybridization of target DNA with the nanogold mixed probes of either α-thalassemia 1 or α-thalassemia 2. No hybridization in both reactions showing blue color indicated absence of abnormal genes causing these α-thalassemias. Positive reaction showing either red or purple color was further analyzed in second hybridization with the nanogold single probe. Positive of α-thalassemia 1 was genotyped with the single probes of both SEA and THAI deletion while those of α-thalassemia 2 were genotyped with both 3.7-kb and 4.2-kb deletion. Results: Genotypic potency of the nanogold mixed and single probes was evaluated using both known diagnosed and suspected clinical samples. The results by naked eye were consistence with those analyzed by standard agarose gel electrophoresis. Conclusions: Potency of the colorimetric nanogold α-thalassemia probes was accurate, precise, sensitive, specific, simple, cheap and field applicable. Color reaction was simply visualized by naked eye. This development is an example of colorimetric molecular diagnosis which can be applied in any genetic detection. © 2014 Elsevier B.V.
