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rSac3, a novel Sac domain phosphoinositide phosphatase, promotes neurite outgrowth in PC12 cells 被引量:1
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作者 Yiyuan Yuan Xiang Gao +6 位作者 Ning Guo Hui Zhang zhiqin xie Meilei Jin Baoming Li LeiYu Naihe Jing 《Cell Research》 SCIE CAS CSCD 2007年第11期919-932,共14页
囊包含域的蛋白质属于 phosphoinositide 磷酸酶(PIPPase 家庭) 的一个最新识别的家庭。尽管有描绘得好的酶的活动,这个哺乳动物的囊领域 PIPPase 家庭的生物功能仍然保持大部分未知。我们识别了新奇的囊包含域的蛋白质,老鼠 Sac3 (rS... 囊包含域的蛋白质属于 phosphoinositide 磷酸酶(PIPPase 家庭) 的一个最新识别的家庭。尽管有描绘得好的酶的活动,这个哺乳动物的囊领域 PIPPase 家庭的生物功能仍然保持大部分未知。我们识别了新奇的囊包含域的蛋白质,老鼠 Sac3 (rSac3 ) 它是广泛地在各种各样的纸巾表示了并且对 endoplasmic 蜂窝胃局部性, Golgi 复杂、再循环的内涵体。rSac3 在 vitro 作为底层与 PI (3 ) P, PI (4 ) P 和 PI (3,5 ) P (2 ) 显示 PIPPase 活动,并且在囊域的催化核心的一个变化废除它的酶的活动。rSac3 的表示起来在刺激的神经生长因素(NGF ) 期间调整了 PC12 细胞 neuronal 区别,并且在这的表示上,蛋白质在 PC12 细胞支持神经突长出。相反地,由反感觉 oligonucleotides 的 rSac3 表示的抑制减少刺激 NGF 的 PC12 房间的神经突长出,并且 rSac3 的活跃地点变化消除它的 neurite-outgrowth-promoting 活动。这些结果显示 rSac3 在通过它的 PIPPase 活动区分神经原支持神经突长出,建议囊领域 PIPPase 蛋白质可以参予从到血浆膜的 endoplasmic 蜂窝胃和 Golgi 建筑群的前面的膜交通国王,并且可以作为 neuronal 房间生长和区别的这个关键过程的管理者工作。 展开更多
关键词 细胞内薄膜 神经突 PC12细胞 磷酸肌醇
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Development of H5 subtype-specific monoclonal antibodies (MAb) and MAb-based assays for rapid detection of H5 avian influenza
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作者 Huaguang Lu Lin Lin +6 位作者 Ronghui Wang Yanbin Li Yanbin Li Bill Scheuchenzuber Jiabo Liu zhiqin xie Joseph A. Rosebrock 《Health》 2012年第10期923-926,共4页
Avian influenza (AI) virology surveillance is the most important method to monitor AI virus (AIV) in poultry so as to effectively prevent and control AI outbreaks. Monoclonal antibodies (MAb)-based assays are highly s... Avian influenza (AI) virology surveillance is the most important method to monitor AI virus (AIV) in poultry so as to effectively prevent and control AI outbreaks. Monoclonal antibodies (MAb)-based assays are highly sensitive and specific for AIV detection, and much practical and economic for test-in-field or onsite. Many such assays have been developed and are still in developing since the H5N1 highly pathogenic AI (HPAI) outbreaks occurred in South East Asia in 2003. A MAb-based dot-enzyme-linked immunosorbent assay (ELISA) has been developed in our lab during late 1990s and early 2000s. Meanwhile, AIV H7 and H5 subtype specific-MAbs have been successfully developed in our laboratory to enhance the Dot-ELISA and other MAb-based assays for AIV detection. Production and purification of the H7 and H5 MAbs were made to provide essential reagents for Dot-ELISA and other immunoassays, and the current development of a novel Biosensor technique for rapid detection of AIV from clinical and field specimens. 展开更多
关键词 Avian Influenza Virus HEMAGGLUTININ HYBRIDOMA Cell Line MONOCLONAL ANTIBODIES DOT-ELISA Biosensor
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