PCR fragments were analyzed on gel

PCR fragments were analyzed on gel electrophoresis carried out by applying 5 lL of sample to 1.5%
agarose gels. Gels were run for about 45 min at 110 V in TAE 1X buffer (0.04 M Tris/acetate, EDTA 1 mM) to check the quality and size of PCR products before DGGE or sequencing.

結果 (中文) 1:

PCR 片段进行分析凝胶电泳进行应用 5 将样品至 1.5%琼脂糖凝胶。凝胶是运行约 45 分钟在 110 V 中泰 1 X 缓冲区 （0.04 M 三/乙酸酯，EDTA 1 毫米） 前，必须核对的质量和大小的 PCR 产物 DGGE 或测序。

結果 (中文) 3:

聚合酶链反应的片段进行了分析，通过施加5的样品的凝胶电泳1.5%琼脂糖凝胶。凝胶在110 V在TAE 1X缓冲运行约45分钟（0.04米三/乙酸、EDTA 1毫米）在DGGE测序质量检查和PCR产物的大小。