19 research outputs found
The Wallach Rearrangement of p-Nitroazoxybenzenes and the Reaction with Chlorosulfonic Acid
departmental bulletin pape
昆虫の変態・休眠の分子機構
平成8年度から平成11年度までの4年間に実施された特定領域研究(A)(1)「昆虫の変態・休眠の分子機構(略称:変態・休眠機構)」は,昆虫の有する旺盛な生存,生活戦略を変態と休眠という高次の生命現象に焦点を合わせ,この分子機構を多面的に解明することを目的として,延べ62名の研究者の参加を得て進められ,多くの研究成果を挙げてきた.「変態・休眠を支配するホルモン分子の動態と環境応答」に関する研究では,脳神経ペプチドホルモンの遺伝子の同定,合成分泌とその調節機構,ホルモンの血中動態及びホルモン受容体の解析を進め,新たな知見を得た.また「変態における自己・非自己の認識転換と形作りの分子機構」に関する研究では,幼虫組織の識別と排除機構,成虫組織の分化発生機構,ミツバチの社会性分化をもたらす遺伝子の同定とその発現機構を解明した.これらの成果の一端は平成12年12月神戸市にいて開催された平成12年度文部省主催の「大学と科学」公開シンポジウム「昆虫から学ぶ生きる知恵」において,研究者のみならず一般市民約500名に対し,公表された.一方,総括班員を中心とした研究成果の最終まとめに関する検討をもとにして,学術審議会科学研究費分科会審査第一部会生物系小委員会による特定領域研究研究終了ヒアリングを受け,その結果,Aの評価を得た.また,本研究の成果は,研究目的や研究経過に加え,本研究参加者の研究結果と発表論文リストを編集した研究成果報告書として発刊し,関連機関や研究者等に配布した.科学研究費補助金 研究種目:特定領域研究(A)(1) 課題番号:08276103 研究代表者:山下 興亜 研究期間:1996-2000年度research repor
Elucidation of photoinduced structural modification in oxide semiconductors for fully solution-processed thin-film transistors
奈良先端科学技術大学院大学博士(工学)doctoral thesi
Analysis and consideration on results of long term mortar strength test
application/pdfIn this research, the strength of mortar specimens made during construction of Otaru port were analyzed. The experiment was planned and initiated by Dr.Isami HIROl in the 19th century. The purpose of this study is to research the long-term strength and durability of mortar specimens. The results of these long-term experiments carried out with various internal factors(type of cement, type of fine aggregate, type of volcanic ash, water cement ratio)and external factors (age and exposure conditions such as in water, in air,and in sea water)are analyzed. The long-term mortar strength test can be summarized as follows : ?tensile strength is affected by water-binder ratio, water-cement ratio, cement proportion, and volcanic ash proportion. ?the reliability of not declining the tensile strength of age 28 days was 52 %,that of 3 months ; 5 %,and that of 1 year ; nearly 0 % at the age 80 years.departmental bulletin pape
a. Agarose gel of RTPCR products to show the effects of RNAi depletion of MCM5 and MCM8 and MCM 5 plus 8 on the MCM5 and 8 levels.
<p>b. FACS profiles of cells targeted with dsRNA against MCM8, and MCM5 plus MCM8. The data presented is one complete representative data set from multiple repetitions.</p
Day 5 growth profiles of MCM targeted cells compared to a control cell line.
<p>The data presented shows combined data from seven independent experiments. The data is expressed as a percentage of the control. Lane 1 is the control and lanes 2-8 are MCM 2-8 resepectively.</p
Quantitation of cell cycle parameters of Drosophila MCM mutants.
<p>Quantitation of cell cycle parameters of Drosophila MCM mutants.</p
a. Schematic detailing the regions of each MCM targeted for dsRNA.
<p>Base positions are quoted relative to the start AUG. Shaded arrows designate the 2<sup>nd</sup> dsRNA made from MCM6/7. b. Agarose gel of RT-PCR products showing the effects of RNAi depletion of individual MCMs on MCM mRNA expression levels. Horizontal numbers designate the MCM targeted by RNAi. Vertical numbers show the RT PCR target. The data presented is one complete representative data set from multiple repetitions. c. Western blot to show the effect of RNAi depletion of individual MCMs on MCM protein expression levels in total cell extracts. Horizontal numbers designate the MCM targeted by RNAi. Vertical numbers show the antibody used for western blotting. Tubulin expression is included as a loading control. The data presented is one complete representative data set from multiple repetitions.</p
FACS analysis profiles of cells targeted with dsRNA against MCM2-7 proteins as compared to control targeted cells.
<p>The data presented is one complete representative data set from multiple repetitions.</p
