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Copyright of Polymer Materials Science & Engineering is the property of Sichuan University, Polymer Research Institute and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

以聚己内酯二元醇(PCL)为软段,二羟甲基丙酸(DMPA)为扩链剂,异佛尔酮二异氰 酸酯(IPDI)为硬段,合成了水性聚氨酯预聚体.通过进一步添加双酚芴(BPFL)反应合成一系 列含 Cardo环水性聚氨酯(WPUS).利用傅里叶变换红外光谱、粒径、热重、力学、X灢射线衍射、 水接触角测定和纸张表面施胶等方法对制备的 WPUS的结构和性能进行表征.结果表明,当 WPUS的 BPFL含量为3%时,WPUS乳液的粒径增大至95.21nm;膜的耐热性最大提高 31.36%;水接触角提升32.13%.不同乳液对纸张表面施胶后与未施胶纸张相比,WPUS3纸 张水接触角提升887.6%;抗张强度最大可达57.1N/mm2,提升46.41%;纸张耐折度最大可 达74次,比未施胶原纸高出60次. [ABSTRACT FROM AUTHOR]

Copyright of Transactions of the Chinese Society of Agricultural Engineering is the property of Chinese Society of Agricultural Engineering and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Objective·To construct inducible CRISPR/Cas9 system for studying gene function in mouse immune cells, combining Dox-inducible single guide RNA (sgRNA) expression vector with Cas9 transgenic mice. Methods·U6-TetO-sgRNA and EF1α -T2A-Puro-BFP-T2A-TetR fragments were obtained by gene synthesis. The two synthetic fragments were assembled into the retroviral vector backbone by using homologous recombination. sgRNA targeting protein coding region of F4/80 and non-targeting control (NC) were designed. Bone marrow cells were isolated from Cas9 transgenic mice and transfected with retrovirus expressing sgRNA. The experimental conditions were divided into Dox-added group (Dox +) and non Dox-added group (Dox-). The knockout effect was tested by flow cytometry and T7 endonuclease I (T7EI) experiments. Results·①Dox-inducible sgRNA retroviral vector and Cas9 transgenic mice were successfully constructed. ② The result of flow cytometry showed that F4/80 was only knocked out in the F4/80 Dox+ population, but not in NC Dox-, NC Dox+ and F4/80 Dox- populations. ③ T7E I results showed that the DNA was cut into two bands in the F4/80 Dox+ group, while the DNA band was intact in the F4/80 Dox-group. Conclusion·An inducible CRISPR/Cas9 system combining Dox-inducible sgRNA retroviral vector with Cas9 transgenic mice are successfully constructed. With this system, inducible gene knockout in mouse immune cells are successfully achieved. [ABSTRACT FROM AUTHOR]

Copyright of China Mechanical Engineering is the property of Editorial Board of China Mechanical Engineering and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of China Pulp & Paper is the property of China Pulp & Paper Magazines Publisher and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)