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    • 3. 发明授权
    • Phage bonded to a nuclear location signal
    • 噬菌体与核定位信号
    • US06235521B1
    • 2001-05-22
    • US09242131
    • 1999-09-10
    • Mahito NakanishiEmi NagoshiTeruo AkutaKatsuo TakedaMamoru Hasegawa
    • Mahito NakanishiEmi NagoshiTeruo AkutaKatsuo TakedaMamoru Hasegawa
    • C12N700
    • C12N15/1037C12N15/85C12N15/86C12N15/87C12N2795/10343
    • A &lgr; phage with a nuclear localization signal has been obtained by constructing a vector capable of expressing a fused protein between a gpD protein constituting the head of a &lgr; phage and a nuclear localization signal sequence, transforming Escherichia coli with this vector, and propagating a mutant &lgr; phage which cannot express the gpD protein in E. coli in this transformant. It has been confirmed that the resulting &lgr; phage is capable of packaging &lgr; phage DNAs of 80% and 100% genome sizes. After further confirming that the nuclear localization signal exposed on the outside of the head of this phage, this phage has been microinjected into cells to analyze its nuclear localization activity. Thus, it has been clarified that this phage has a nuclear localization activity.
    • 通过构建能够在构成羔羊噬菌体的头部的gpD蛋白质和核定​​位信号序列之间表达融合蛋白的载体,通过该载体转化大肠杆菌并扩增突变体,获得具有核定位信号的羔羊噬菌体 在该转化体中不能在大肠杆菌中表达gpD蛋白的羔羊噬菌体。 已经证实,所得的羔羊噬菌体能够包装80%和100%基因组大小的羔羊噬菌体DNA。 在进一步证实核定位信号暴露在该噬菌体头部的外部时,该噬菌体已被微量注入细胞以分析其核定位活性。 因此,已经澄清这种噬菌体具有核定位活动。
    • 4. 发明授权
    • Phage with nuclear localization signal
    • 噬菌体与核定位信号
    • US06759231B2
    • 2004-07-06
    • US09844813
    • 2001-04-27
    • Mahito NakanishiEmi NagoshiTeruo AkutaKatsuo TakedaMamoru Hasegawa
    • Mahito NakanishiEmi NagoshiTeruo AkutaKatsuo TakedaMamoru Hasegawa
    • C12N120
    • C12N15/1037C12N15/85C12N15/86C12N15/87C12N2795/10343
    • A &lgr; phage with a nuclear localization signal has been obtained by constructing a vector capable of expressing a fused protein between a gpD protein constituting the head of a &lgr; phage and a nuclear localization signal sequence, transforming Escherichia coli with this vector, and propagating a mutant &lgr; phage which cannot express the gpD protein in E. coli in this transformant. It has been confirmed that the resulting &lgr; phage is capable of packaging &lgr; phage DNAs of 80% and 100% genome sizes. After further confirming that the nuclear localization signal exposed on the outside of the head of this phage, this phage has been microinjected into cells to analyze its nuclear localization activity. Thus, it has been clarified that this phage has a nuclear localization activity.
    • 已经通过构建能够在构成λ噬菌体的头部的gpD蛋白质和核定​​位信号序列之间表达融合蛋白质的载体,用该载体转化大肠杆菌并扩增突变体来获得具有核定位信号的λ噬菌体 λ噬菌体在该转化体中不能在大肠杆菌中表达gpD蛋白。 已经证实所得的λ噬菌体能够包装80%和100%基因组大小的λ噬菌体DNA。 在进一步证实核定位信号暴露在该噬菌体头部的外部时,该噬菌体已被微量注入细胞以分析其核定位活性。 因此,已经澄清这种噬菌体具有核定位活动。
    • 6. 发明申请
    • AQUEOUS PREPARATION COMPRISING eMIP AS ACTIVE INGREDIENT
    • 包含eMIP作为主动成分的水质准备
    • US20100316592A1
    • 2010-12-16
    • US12502959
    • 2009-07-14
    • Teruo AKUTAYoshiko Aoki
    • Teruo AKUTAYoshiko Aoki
    • A61K38/16
    • A61K38/195A61K9/0019A61K9/08A61K47/02A61K47/183
    • An objective of the present invention is to provide aqueous preparations comprising eMIP, a derivative of macrophage inflammatory protein 1α (MIP-1α) which has an immunopotentiation activity, and stabilizer(s). The present inventors conducted dedicated studies to achieve the above-described objective. As a result, the present inventors discovered that eMIP degradation is suppressed by addition of at least one or more additives selected from sodium chloride, L-histidine, L-arginine, L-arginine hydrochloride, L-lysine hydrochloride, citric acid, and sodium edetate (EDTA). Furthermore, the present inventors demonstrated that phosphate buffer of pH 5 to pH 7 is a preferable pH adjuster for the aqueous eMIP preparations of the present invention.
    • 本发明的目的是提供包含eMIP,具有免疫增强活性的巨噬细胞炎症蛋白1α(MIP-1α)的衍生物和稳定剂的含水制剂。 本发明人进行了专门的研究以实现上述目的。 结果,本发明人发现通过添加选自氯化钠,L-组氨酸,L-精氨酸,L-精氨酸盐酸盐,L-赖氨酸盐酸盐,柠檬酸和钠中的至少一种或多种添加剂,可以抑制eMIP降解 乙二胺四乙酸(EDTA)。 此外,本发明人证明,pH5〜pH7的磷酸盐缓冲液是本发明的含水eMIP制剂的优选的pH调节剂。