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141.
  • Overexpression of a Domain ... Overexpression of a Domain of Unknown Function 266-containing protein results in high cellulose content, reduced recalcitrance, and enhanced plant growth in the bioenergy crop Populus
    Yang, Yongil; Yoo, Chang Geun; Guo, Hao-Bo ... Biotechnology for biofuels, 03/2017, Letnik: 10, Številka: 1
    Journal Article

    Domain of Unknown Function 266 (DUF266) is a plant-specific domain. DUF266-containing proteins (DUF266 proteins) have been categorized as ‘not classified glycosyltransferases (GTnc)’ due to amino ...
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142.
  • Thermal Oxidation of WSe2 Nano-sheets Adhered on SiO2/Si Substrates
    Liu, Yingnan; Tan, Cheng; Chou, Harry ... arXiv.org, 07/2015
    Paper, Journal Article
    Odprti dostop

    Due to the drastically different intralayer versus interlayer bonding strengths, the mechanical, thermal, and electrical properties of two-dimensional (2D) materials are highly anisotropic between ...
Celotno besedilo
143.
Celotno besedilo
144.
  • Construction of maize unive... Construction of maize universal expression vector PGM-35Sbar and maize transformation
    Wang Xiaohan, Capital Normal University, Beijing (China), College of Life Science; Luo Chang, Beijing Academy of Agriculture and Forestry Sciences, Beijing ( China), Beijing Agro-Biotechnology Research Center; Cheng Xi, Beijing Academy of Agriculture and Forestry Sciences, Beijing ( China), Beijing Agro-Biotechnology Research Center Hunan agricultural science & technology newsletter : HASTN, Aug. 2012, Letnik: 13, Številka: 8
    Journal Article

    目的构建玉米通用表达载体,以期为利用转基因手段提高玉米对非生物胁迫的耐受性奠定基础。方法通过对现有的pGreen0229植物表达载体进行改造,构建含有CaMv35S启动子驱动的抗草胺膦筛选基因bar、可用于连接目的基因的玉米表达载体PGM-35Sbar,并通过花粉管通道法转化吉444玉米自交系。结果PGM-35Sbar玉米通用载体构建成功,转化玉米植株后,得到抗性植株14棵,经PCR检测其中有12棵为阳性植株。结论该研究为快速构建含有特定目的基因的玉米表达载体奠定了基础。 Objective The paper was to construct maize universal expression vector, in order to provide basis for using transgenic methods to improve abiotic stress tolerance of maize. Method Based on the transformation of existing pGreen0229 plant expression vector, phosphinothricin-resistant selectable marker-bar gene driving by CaMv35S promoter was constructed, which could be used to connect target gene of maize expression vector PGM-35Sbar, and transform Ji444 maize inbred lines by pollen tube pathway. Result The universal expression vector for PGM- 35Sbar maize had been successfully constructed. When the maize plants were transformed, 14 resistant plants were obtained, and 12 plants were identified to be positive plants by PCR detection. Conclusion The study provide
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