Abe A, Takashima M
Department of Clinical Chemistry, Gifu College of Medical Technology.
Rinsho Byori. 1998 Mar;46(3):283-8.
Serum apo(a) isoform sizes were determined by SDS-polyacryl amide gel electrophoretic (PAGE) method, followed by a high sensitive immunoblotting. The relation between the number of apo(a) kringle IV encoding sequences in the apo(a) gene, as assessed by pulsed field gel electrophoresis and genomic blotting (genotype), and the apo(a) isoforms (phenotype) in SDS-PAGE was evaluated in 78 individuals. The correlation of apo(a) allele number between phenotype and genotype method was high (r = 0.513) in 178 expressed apo(a) alleles. This nomenclature is achieved by using standard serum of kringle IV repeats. We conclude that this method is an approach to genotyping to designate the phenotypes by kringle IV repeats.
血清载脂蛋白(a)异构体大小通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)法测定,随后进行高灵敏度免疫印迹分析。通过脉冲场凝胶电泳和基因组印迹法(基因型)评估载脂蛋白(a)基因中载脂蛋白(a)kringle IV编码序列的数量与SDS-PAGE中载脂蛋白(a)异构体(表型)之间的关系,对78名个体进行了研究。在178个表达的载脂蛋白(a)等位基因中,表型和基因型方法之间的载脂蛋白(a)等位基因数量相关性很高(r = 0.513)。这种命名法是通过使用kringle IV重复序列的标准血清来实现的。我们得出结论,该方法是一种通过kringle IV重复序列对表型进行基因分型的方法。