釉原蛋白
分子生物学
琼脂糖凝胶电泳
聚合酶链反应
打字
Y染色体
生物
凝胶电泳
温度梯度凝胶电泳
核酸凝胶电泳
电泳
琼脂糖
染色体
遗传学
底漆(化妆品)
DNA
聚丙烯酰胺凝胶电泳
基因
化学
生物化学
酶
有机化学
16S核糖体RNA
作者
Barry Eng,Peter Ainsworth,John S. Waye
摘要
Sex-typing of biological samples can be accomplished using the polymerase chain reaction (PCR) to amplify DNA sequences that are specific for the Y-chromosome. One such system is based on PCR amplification of the X-chromosome amelogenin gene and the amelogenin-like sequences located near the centromere of the Y-chromosome. The X and Y PCR products can be distinguished from each other on the basis of a 177 basepair (bp) insertion in the X relative to the Y. In this report, we demonstrate that the amelogenin PCR products migrate anomalously using non-denaturing polyacrylamide gel electrophoresis (ND-PAGE) as opposed to agarose gel electrophoresis or denaturing PAGE. These results may be relevant to the choice of electrophoretic system used to analyze highly polymorphic loci for individual identification.
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