In this paper, a new progress in scattering measurement of ocean surface wind vector using a space borne scanning scatterometer (CNSCAT) has been described. The CNSCAT developed during the past five years in the labor...In this paper, a new progress in scattering measurement of ocean surface wind vector using a space borne scanning scatterometer (CNSCAT) has been described. The CNSCAT developed during the past five years in the laboratory for Microwave Remote Sensing and Information Technology (MIRIT), CSSAR,The Chinese Academy of Sciences, will be launched in early next decade. This paper also discussed CNSCAT system design, system calibration and some theoretical analysis.展开更多
为深入研究山羊AP1M1(adaptor related protein complex 1 subunit mu 1)在机体生长和繁殖中的作用,采用RT-PCR方法克隆了山羊AP1M1基因,并对其序列和编码蛋白进行分析;构建了pET-30α-AP1M1原核表达载体,免疫实验兔,制备AP1M1基因多克...为深入研究山羊AP1M1(adaptor related protein complex 1 subunit mu 1)在机体生长和繁殖中的作用,采用RT-PCR方法克隆了山羊AP1M1基因,并对其序列和编码蛋白进行分析;构建了pET-30α-AP1M1原核表达载体,免疫实验兔,制备AP1M1基因多克隆抗体;采用qPCR和Western blot检测比较AP1M1在山羊不同组织及睾丸不同发育时期的表达特征。结果显示,山羊AP1M1基因CDS为1 272 bp,编码423个氨基酸,具有1个Clat-adaptor结构域、1个Adap-comp结构域和5个蛋白质-蛋白质结合位点,在哺乳动物中极为保守。间接ELISA和Western blot结果表明,制备的兔抗pET-30α-AP1M1多克隆抗体效价为1∶128 000,可以与重组蛋白特异性结合。表达模式检测结果显示,AP1M1在成年山羊各组织中均有不同程度的表达,其中在肾脏的表达量最高,其次是睾丸,均极显著高于其他组织(P<0.01);此外,AP1M1在山羊不同发育时期睾丸组织中均有表达,但在性成熟时显著增加(P<0.01),体成熟时达到最高。本试验为进一步探索该基因在山羊睾丸中的功能奠定基础。展开更多
文摘In this paper, a new progress in scattering measurement of ocean surface wind vector using a space borne scanning scatterometer (CNSCAT) has been described. The CNSCAT developed during the past five years in the laboratory for Microwave Remote Sensing and Information Technology (MIRIT), CSSAR,The Chinese Academy of Sciences, will be launched in early next decade. This paper also discussed CNSCAT system design, system calibration and some theoretical analysis.
文摘为深入研究山羊AP1M1(adaptor related protein complex 1 subunit mu 1)在机体生长和繁殖中的作用,采用RT-PCR方法克隆了山羊AP1M1基因,并对其序列和编码蛋白进行分析;构建了pET-30α-AP1M1原核表达载体,免疫实验兔,制备AP1M1基因多克隆抗体;采用qPCR和Western blot检测比较AP1M1在山羊不同组织及睾丸不同发育时期的表达特征。结果显示,山羊AP1M1基因CDS为1 272 bp,编码423个氨基酸,具有1个Clat-adaptor结构域、1个Adap-comp结构域和5个蛋白质-蛋白质结合位点,在哺乳动物中极为保守。间接ELISA和Western blot结果表明,制备的兔抗pET-30α-AP1M1多克隆抗体效价为1∶128 000,可以与重组蛋白特异性结合。表达模式检测结果显示,AP1M1在成年山羊各组织中均有不同程度的表达,其中在肾脏的表达量最高,其次是睾丸,均极显著高于其他组织(P<0.01);此外,AP1M1在山羊不同发育时期睾丸组织中均有表达,但在性成熟时显著增加(P<0.01),体成熟时达到最高。本试验为进一步探索该基因在山羊睾丸中的功能奠定基础。