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Development of the Micro-Silk Through the Breeding of Transgenic Silkworm

机译:通过转基因蚕的繁殖开发微丝

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The purpose of this research is to develop the micro-silk through the breeding of the transgenic silkworm. First of all, to construct transformation vector system of silkworm, we did cloning the sericin promoter in silkworm and sorting the selection marker gene (in order that sorting the transformation silkworm) and then cloning again. Second, we analyzed the fibroin gene of silkworm and IGF-1 gene of human After cloning. Then, we made and analyzed transformants of silkworm which gene expression as IGF-1 of human and the fibroin of silkworm. We inserted the protein expression vector which IGF-1 of human and the fibroin of silkworm into silkworm eggs using the microinjection. Using PCR and Southern blot methods, we analyzed expression vector in DNA level. In addition, we analyzed it using the RT-PCR methods in order to confirm gene expression in RNA level. The protein expression was analyzed in protein level through the western blot and ELISA methods. Through transformation on two separate occasions on spring and summer, we determined growth and ecology between Uzbekistan silkworm and Korean transformation silkworm. Lastly, we compared fabric of Uzbekistan silk, Chinese silk and Japanese 6A which we developed. Also we analyzed sericin content, strength and elongation and thickness of transformation silk single yarn.
机译:本研究的目的是通过转基因蚕的繁殖来发展微丝。首先,为了构建家蚕的转化传染媒介系统,我们确实克隆了蚕的丝氨酸启动子并将选择标记基因分类(按顺序排序转化蚕),然后再次克隆。其次,我们分析了克隆后蚕的纤维素基因和人IGF-1基因。然后,我们制造和分析了蚕的转化体,其基因表达为人类和蚕素蛋白的IGF-1。我们将蛋白质表达载体插入使用微注射的IGF-1的IGF-1和蚕丝蛋白进入蚕卵。使用PCR和Southern印迹方法,我们分析了DNA水平中的表达载体。此外,我们使用RT-PCR方法分析了它,以确认RNA水平中的基因表达。通过Western印迹和ELISA方法在蛋白质水平中分析蛋白质表达。通过在春夏的两个独立场合转变,我们确定了乌兹别克斯坦蚕和韩国转型家蚕之间的增长和生态。最后,我们比较了我们开发的乌兹别克斯坦丝绸,中国丝绸和日本6A的面料。我们还分析了转化丝单纱的胺含量,强度和伸长率和厚度。

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