Abstract:
PURPOSE: A single PCR primer amplifying the potato specific DNA and a duplex PCR method for screening genetically modified potato(GMP) using the same are provided, thereby increasing the accuracy of GMP screening and reducing screening costs. CONSTITUTION: A single PCR primer amplifying the potato specific DNA has the nucleotide sequence set forth in SEQ ID NO: 2, wherein the potato specific DNA has the nucleotide sequence set forth in SEQ ID NO: 1. A duplex PCR method for screening genetically modified potato is characterized by using the single PCR primer, wherein the primer may be any one selected from single PCR primer having the nucleotide sequence set forth in SEQ ID NO: 2, CaMV 35S promoter or primer amplifying NOS terminator gene region.
Abstract translation:目的:提供扩增马铃薯特异性DNA的单一PCR引物和使用该方法筛选遗传修饰马铃薯(GMP)的双重PCR方法,从而提高GMP筛选的准确性并降低筛选成本。 构成:扩增马铃薯特异性DNA的单一PCR引物具有SEQ ID NO:2所示的核苷酸序列,其中马铃薯特异性DNA具有SEQ ID NO:1所示的核苷酸序列。用于筛选遗传修饰的双重PCR方法 马铃薯的特征在于使用单一PCR引物,其中引物可以是选自具有SEQ ID NO:2所示核苷酸序列的单一PCR引物,CaMV 35S启动子或扩增NOS终止子基因区的引物中的任一种。
Abstract:
PURPOSE: A portable structure for the cultivation of edible plants is provided to improve cultivation efficiency by including a control system providing a preset condition to cultivate the edible plants under an optimized condition. CONSTITUTION: A container box(10) comprises an incubator(11) in which selected edible plants grow. A control system(20) is installed in the container box, and controls the inner condition of the incubator. The control system provides a preset condition by the kind of the edible plants and a cultivation method. The container box is an export container which corresponds to the standard specification recommended by the international standardization organization. A solar power generation system(30) is installed on the container box, and provides necessary electric power. The container box further includes a laboratory(12) equipped with facilities for the research of the edible plants. [Reference numerals] (20) Control system; (30) Solar power generation system
Abstract:
본 발명은 식용작물 재배용 이동식 구조물에 관한 것으로서, 더욱 상세하게는 선택된 식용작물을 생장시키는 성장실을 구비하는 육면체 형상의 컨테이너 박스와, 상기 컨테이너 박스에 설치되어 상기 성장실 내부 조건을 조절하는 제어 시스템;을 포함하여 구성되고, 상기 제어 시스템이 상기 식용작물의 종류 및 재배방식에 따라 미리 셋팅된 조건을 제공함으로써, 용이하게 이동시킬 수 있어 어느 곳에나 제약없이 설치가 가능하고, 예산 및 시간을 절약하면서도 최적화된 조건 하에서 식용작물 재배가 가능해 효율을 극대화시킬 수 있다.
Abstract:
PURPOSE: A single PCR primer amplifying the potato specific DNA and a duplex PCR method for screening genetically modified potato(GMP) using the same are provided, thereby increasing the accuracy of GMP screening and reducing screening costs. CONSTITUTION: A single PCR primer amplifying the potato specific DNA has the nucleotide sequence set forth in SEQ ID NO: 2, wherein the potato specific DNA has the nucleotide sequence set forth in SEQ ID NO: 1. A duplex PCR method for screening genetically modified potato is characterized by using the single PCR primer, wherein the primer may be any one selected from single PCR primer having the nucleotide sequence set forth in SEQ ID NO: 2, CaMV 35S promoter or primer amplifying NOS terminator gene region.
Abstract translation:目的:提供扩增马铃薯特异性DNA的单一PCR引物和使用该方法筛选转基因马铃薯(GMP)的双链PCR方法,从而提高GMP筛选的准确性并降低筛选成本。 构成:扩增马铃薯特异性DNA的单个PCR引物具有SEQ ID NO:2所示的核苷酸序列,其中马铃薯特异性DNA具有SEQ ID NO:1所示的核苷酸序列。用于筛选遗传修饰的双链PCR方法 马铃薯的特征在于使用单一PCR引物,其中引物可以是选自具有SEQ ID NO:2所示核苷酸序列,CaMV 35S启动子或引物扩增NOS终止子基因区的单一PCR引物中的任一种。