Detection of β-thalassemia and hemoglobin E genes in Thai by a DNA amplification technique
✍ Scribed by Pranee Winichagoon; Jiraporn Kownkon; Pathai Yenchitsomanus; Varaporn Thonglairoam; Nopadol Siritanaratkul; Suthat Fucharoen
- Publisher
- Springer
- Year
- 1989
- Tongue
- English
- Weight
- 222 KB
- Volume
- 82
- Category
- Article
- ISSN
- 0340-6717
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✦ Synopsis
Enzymatic DNA amplification and polyacrylamide gel electrophoresis, which demonstrate different sizes of DNA fragments, were used to detect the common mutations causing beta-thalassemia and hemoglobin (Hb) E in Thai people. The 4-bp deletion at codons 41 and 42 can be detected directly by polyacrylamide gel electrophoresis and ethidium bromide staining. Whereas the nonsense mutations at codon 17 (AAG----TAG) and Hb E (GAG----AAG at codon 26) were detected after digestion of the amplified DNA with the enzymes MaeI and MnlI, respectively.
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