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Detection of genetically modified coho salmon using polymerase chain reaction (PCR) amplification

机译:使用聚合酶链反应(PCR)扩增检测转基因银大麻哈鱼

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A PCR-based protocol for the identification of genetically modified salmon carrying a growth hormone transgene was developed. Several primer pairs were examined, and the primers that gave consistent results were selected to conduct routine testing. Comparison among several DNA extraction procedures, as well as different buffer compositions, led to the adoption of TriZol as the method of choice. Low potassium and high magnesium chloride concentrations were very important in the overall success of the PCR reaction, whereas buffer pH, ranging from 8.3 to 9.2, had little impact on the amplification reaction. The optimal primer annealing temperature was 52 degreesC. Although fish muscle tissues were the. primary source for DNA samples, detection of the transgene was also possible in bones, skin, fins, and other organs. No benefits were achieved by the addition of additives such as dimethyl sulfoxide and betaine to the PCR reaction. This optimized PCR method was used to identify all samples tested (61 samples and 17 controls) with 100% accuracy. [References: 17]
机译:开发了一种基于PCR的方案,用于鉴定带有生长激素转基因的转基因鲑鱼。检查了几个引物对,并选择了给出一致结果的引物进行常规测试。几种DNA提取程序以及不同缓冲液组成之间的比较导致采用TriZol作为选择方法。低钾和高氯化镁浓度对于PCR反应的总体成功非常重要,而缓冲液的pH值(范围从8.3至9.2)对扩增反应影响很小。最佳的底漆退火温度为52摄氏度。虽然是鱼的肌肉组织。作为DNA样品的主要来源,转基因的检测也可能在骨骼,皮肤,鳍和其他器官中进行。通过向PCR反应中添加二甲基亚砜和甜菜碱等添加剂无法获得任何好处。这种优化的PCR方法用于以100%的准确性鉴定所有测试样品(61个样品和17个对照)。 [参考:17]

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