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未成熟裂殖体
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  “未成熟裂殖体”译为未确定词的双语例句
     The electron-microscopical observation showed that the 185kDa protein recognized by McAb F6-D3 was located on the surface of free and intracellular merozoites as well as the cytoplasm, plasma membrane, and parasitophorous vaccuole membrane of immature schizonts.
     结果表明单克隆抗体F6-D3识别的185kDa蛋白定位于游离的和细胞内的裂殖子表面以及未成熟裂殖体的细胞质、质膜及带虫泡膜。
短句来源
     The 82/41 kDa proteins identified by McAb F6-C2 was located within the rhoptries of immature schizonts and mature merozoites.
     而单克隆抗体F6-C2识别的82/41 kDa蛋白则定位于未成熟裂殖体及成熟裂殖子的棒状体中。
短句来源
     By indirect immnoperoxidase staining,different forms of exoerythrocytic(EE)stage of Plasmodium vivax (Southern China isolates)are revealed in d8 cultured material. The mature schizonts are elongated in shape measuring 42-48 μm in diameter,immature schizonts 14-28 μm and hypnozoites 4 7 μm.
     以免疫酶染色法,观察到HepG2-A16体外培养8d的间日疟原虫(华南分离株)红外期发育为大小不等的几种类型:直径42-48μm的成熟裂殖体、14-28μm的未成熟裂殖体以及4-7μm的休眠体。
短句来源
  相似匹配句对
     FORMATION OF NON-MATURE GAS AND OIL
     未成熟油气的生成
短句来源
     Immature macroschizont, mature macroschizont and free large merozoites in haemolymph of engorged females were discovered.
     在血淋巴中发现了未成熟裂殖体、我熟大裂殖体和游离大裂殖子。
短句来源
     Study on removal of immature fiber
     未成熟纤维去除的研究
短句来源
     The 82/41 kDa proteins identified by McAb F6-C2 was located within the rhoptries of immature schizonts and mature merozoites.
     而单克隆抗体F6-C2识别的82/41 kDa蛋白则定位于未成熟裂殖体及成熟裂殖子的棒状体中。
短句来源
     2. against late tro-phozoites and schizonts;
     2.针对晚期滋养体及裂殖体;
短句来源
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  immature schizont
Both proteins colocalized with Bodipy-ceramide in trophozoite and immature schizont-infected erythrocytes, but not in segmenters.
      


According to Jensen and Trager's candle jar method, five continuous cultivation, in vitro experiments were conducted with Plasmodium berghei. In all of the experiments, the parasites could be seen to go through their erythrocytic cycle, but only a few of merozoites were able to enter the other red blood cells to complete their intra-erythrocytic cycle. These experiments showed 1~2 schizogony of the parasites ia vitro. Parasites in the fractional blood of the 7th day's culture (parasitemia 0.1%) were determined...

According to Jensen and Trager's candle jar method, five continuous cultivation, in vitro experiments were conducted with Plasmodium berghei. In all of the experiments, the parasites could be seen to go through their erythrocytic cycle, but only a few of merozoites were able to enter the other red blood cells to complete their intra-erythrocytic cycle. These experiments showed 1~2 schizogony of the parasites ia vitro. Parasites in the fractional blood of the 7th day's culture (parasitemia 0.1%) were determined by aseptical intraperitoneal injection into the clean mice. The blood parasitemia was mo-nitored after maintaing 7 days. The results were as fellows: (1) The parasitemia went upgrade over 5%. (2) In the blood slide, a few of male and female gametocytes could be seen. (3) The experimental mice died about 7 days after artificial infections. what has been said above, shows that though the erythrocytic stages of plasmodium berghei had been cultivated in vitro for continuous 7 days, the parasites still maintained infectivity and pathogenicity to the host.

按烛缸法对柏氏疟原虫(Plasmodium berghei)红内期进行了体外培养的初步研究。先后5次,每次连续培养7天。除培养的第2天,其原虫率稍有增长外,随后便逐日下降;与此同时,培养的第4天,环状体有增多外,其后也逐日减少,而未成熟裂殖体及成熟裂殖体相对地逐日增加。培养结果提示有1~2个周期的裂体增殖。另将第7天的培养物无菌注入健康正常小白鼠腹腔内,7天后血检,原虫率明显上升(>5%),各红内期形态均可见到,还偶见到配子体,鼠间继续人工传代,原虫活力不减,实验鼠均于1周左右自然致死,反映原虫经体外培养7天后对宿主仍具有很强的毒力。

Plasmodium falciparum FCCl/HN-infected human erythrocytes were embedded with LR White resin at low temperature. The 185 kDa and 82/41 kDa proteins in erythrocytic stages of P. falciparum were then immuno-labeled by using the protective monoclonal antibodies (McAb)F6-D3 and F6-C2 with protein A-colloidal gold probe. The electron-microscopical observation showed that the 185kDa protein recognized by McAb F6-D3 was located on the surface of free and intracellular merozoites as well as the cytoplasm, plasma membrane,...

Plasmodium falciparum FCCl/HN-infected human erythrocytes were embedded with LR White resin at low temperature. The 185 kDa and 82/41 kDa proteins in erythrocytic stages of P. falciparum were then immuno-labeled by using the protective monoclonal antibodies (McAb)F6-D3 and F6-C2 with protein A-colloidal gold probe. The electron-microscopical observation showed that the 185kDa protein recognized by McAb F6-D3 was located on the surface of free and intracellular merozoites as well as the cytoplasm, plasma membrane, and parasitophorous vaccuole membrane of immature schizonts. The 82/41 kDa proteins identified by McAb F6-C2 was located within the rhoptries of immature schizonts and mature merozoites. These results demonstrated ultrastructurally that the 185 kDa and 82/41 kDa protective antigens were merozoite surface antigen and merozoite rhoptry antigens of P. falciparum FCC1/HN, respectively.

用LR White树脂低温包埋感染人恶性疟原虫FCC1/HN株的红细胞,用保护性单克隆抗体F6-D3和F6-C2并结合蛋白A-胶体金探针免疫标记恶性疟原虫红内期185kDa和82/41kDa蛋白。结果表明单克隆抗体F6-D3识别的185kDa蛋白定位于游离的和细胞内的裂殖子表面以及未成熟裂殖体的细胞质、质膜及带虫泡膜。而单克隆抗体F6-C2识别的82/41 kDa蛋白则定位于未成熟裂殖体及成熟裂殖子的棒状体中。从超微结构上表明185 kDa和82/41 kDa保护性抗原分别为恶性疟原虫FCC1/HN株的裂殖子表面抗原和裂殖子棒状体抗原。

By indirect immnoperoxidase staining,different forms of exoerythrocytic(EE)stage of Plasmodium vivax (Southern China isolates)are revealed in d8 cultured material.The mature schizonts are elongated in shape measuring 42-48 μm in diameter,immature schizonts 14-28 μm and hypnozoites 4 7 μm.EE schizonts are stained dark brown only after conjugated by monoclonal antibody(McAb) 4B2 specific against erythrocytic stages of P. vivax while hypnozoites are...

By indirect immnoperoxidase staining,different forms of exoerythrocytic(EE)stage of Plasmodium vivax (Southern China isolates)are revealed in d8 cultured material.The mature schizonts are elongated in shape measuring 42-48 μm in diameter,immature schizonts 14-28 μm and hypnozoites 4 7 μm.EE schizonts are stained dark brown only after conjugated by monoclonal antibody(McAb) 4B2 specific against erythrocytic stages of P. vivax while hypnozoites are only stained after conjugated by McAb 2F2 against sporozoite.These results show that the antigenic components of these two forms of EE plasmodia are quite different.The ratio of EE schizont and hypnozoite found within hepatoma cells (HepG2-A16) is 1.5 to 1. Referred to the clinical manifestations of the isolate,among 5 volunteers not radically cured,two had long incubation period (283 d and 304 d, respectively)and three relapsed 235 260 and 365 days after the primary attack.These data are unanimous with the comparatively large ratio of hypnozoites in the cultured material.

以免疫酶染色法,观察到HepG2-A16体外培养8d的间日疟原虫(华南分离株)红外期发育为大小不等的几种类型:直径42-48μm的成熟裂殖体、14-28μm的未成熟裂殖体以及4-7μm的休眠体。EE裂殖体仅与抗间日疟子孢子结合后才染成棕黄色,提示两者的抗原性有显著差异。在HepG2-A16细胞内,EE裂殖体与休眠体的数量比约为1.5∶1。参看经蚊叮咬感染的11名志愿者中除6人服足量伯氨喹根治外,2人为长潜伏期,潜伏期分别为283d和304d。3名因服伯氨喹剂量不足而复发,潜隐期各为235、260及365d。这些临床表现与体外培养物中休眠体占相当大的比例是一致的。

 
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