The polymorphism of human GOTM was investigated in red blood cells by means of routine starch gel electrophoresis. The formal model of two common alleles, GOTM1 and GOTM2, at an autosomal locus GOTM was confirmed by examination of 640 mother-child pairs. The frequency of GOTM1 in this sample from so
Genetic polymorphism of mitochondrial glutamate-oxaloacetate transaminase in Japanese
β Scribed by Tasuku Toyomasu; Shigeki Sakakibara; Hiroyuki Kagamiyama; Hideo Matsumoto
- Publisher
- Springer
- Year
- 1984
- Tongue
- English
- Weight
- 207 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0340-6717
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Glutamate oxaloacetic transaminase (L-aspertate: 2-oxoglutarate aminotransferase, E.C. 2.6.1.1; GOT) was found to occur in five distinct electrophoretic forms in different tissue extracts from a number of highly inbred strains of Zea mays L. No major qualitative differences were detected in the vari
Malaysians of Malay, Chinese, and Indian ancestries were electrophoretically phenotyped for Amy1 and saliva esterase region 1 (Set-1) from saliva, Amy2 from plasma, soluble and mitochondrial GOT and PGM3 from leukocyte and placenta. Kadazans and Bajaus, the indigenous people of Sabah, East Malaysia