处死
- 与 处死 相关的网络例句 [注:此内容来源于网络,仅供参考]
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He executed his plans with sureness of insight, firmness of resolution, and tenacity of purpose.
他处死了他的计划的确定与顿悟的,坚挺的决议,以及不屈不挠的目的。
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Cerebral hemorrhage rat models were established via injection of autologous arterial blood in caudate nucleus. Two days after modeling, 5 μL BrdU-labeled human embryonic NSCs suspension was transplanted at four points surrounding hematoma cavity in the rats. After 1 and 2 weeks, rats were sacrificed. Adjacent sections were doubly stained by BrdU/microtubule-associated protein 2 (MAP-2) and BrdU/glial fibrillary acidic protein.
通过注射自体动脉血到尾状核制作大鼠脑出血模型,出血后2 d将标有5'-溴脱氧尿嘧啶的人胚神经干细胞悬液移植到血肿腔周围的4点,1,2周后处死大鼠,相邻脑组织切片行5'-溴脱氧尿嘧啶/微管相关蛋白2和5'-溴脱氧尿嘧啶/胶质纤维酸性蛋白免疫组织化学双染。
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METHODS: Cerebral cortex cells of 8-week aborted human fetus were harvested and cultured in vitro to obtain human embryonic NSCs. Cerebral hemorrhage rat models were established via injection of autologous arterial blood in caudate nucleus. Two days after modeling, 5 μL BrdU-labeled human embryonic NSCs suspension was transplanted at four points surrounding hematoma cavity in the rats.
通过注射自体动脉血到尾状核制作大鼠脑出血模型,出血后2 d将标有5'-溴脱氧尿嘧啶的人胚神经干细胞悬液移植到血肿腔周围的4 点,1,2周后处死大鼠,相邻脑组织切片行5'-溴脱氧尿嘧啶/微管相关蛋白2和5'-溴脱氧尿嘧啶/胶质纤维酸性蛋白免疫组织化学双染。
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All data were analyzed by SPSS 10.0 statistical software package. Test of normality and one-way ANOVA were performed among groups.
每组动物在行最后一次扫描后立即过量麻醉处死,断头取脑,标本送常规病理及免疫组化检查,光镜观察。
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INTERVENTIONS: 4 vessel occlusion(4VO) brain ischemic models in rats stained with thionine staining and GFAP immunohistochemistry staining. were used. Sixty-four rats, of which bilateral vertebral arteries were occluded permanently by electrocautery, were divided into the following 8groups: sham operation group, cerebral ischemic preconditioninggroup, ischemic insult group; BIT group; MTPG + sham operation group;MTPG+BIT group; MTPG+ischemia group and -4C3HPG+BIT coup. All the rats were killed 7 days after the operation or the final ischemic treatment. Cerebral sections were selected and stained with thionine staining and GFAP immunohistochemistry staining.
干预:采用大鼠四血管闭塞全脑缺血模型,应用硫堇染色和胶质纤维酸性蛋白免疫组化法。64只大鼠椎动脉凝闭后分为假手术组、单纯预处理组、单纯缺血组、脑缺血耐受组,MTPG+假手术组、MTPG+脑缺血耐受组、MTPG+缺血组和-4C3HPG+脑缺血耐受组,所有动物均在手术后或末次缺血后7 d处死取材,行脑组织切片,硫堇染色和胶质纤维酸性蛋白免疫组化染色。
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Fabrication of tissue section:after spinal cord injury ld,3d,5d,8d,14d,21d,we sacrificed rats in batch.4% formaldehydum polymerisatum were pured into the cardiac muscle and fixed for 24h.Then obtain the specimen of spinal cord from T_5 to T_(13).Establishing slices,HE dyeing,bcl-2 dectation,terminal doxynucleotidyl transferase-mediated dUTP nick end labeling.On the fourteenth day after spinal cord injury,we detect Gale grading score and tiltboard experiment.
组织切片的制备:脊髓损伤后1d,3d,5d,8d,14d,21d共6个时间段分批处死动物。4%多聚甲醛心肌灌注固定24h,切取每只大鼠T_5~T_(13)节段脊髓组织,常规制成切片,给于HE染色,Bcl-2检测,TUNEL原位末端标记以及伤后第14天检测Gale评分和斜板实验,检测大鼠脊髓损伤后细胞凋亡和脊髓神经功能恢复情况。
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Four rats in each group were re-anesthetized. They were killed and their brain was gained. Survival neurons were detected with toluidine blue staining.
然后每组取4只大鼠,采用相应的麻醉剂进行麻醉后处死取脑,甲苯胺蓝染色检测半暗带内的存活神经元。
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The density of bone mineral substance and femoral geometry size and polar moment of inertia and torsional section modulus and rectangular moment of intertia and rectangular section modulus and biomechanics capabilities were determined.
连续给药90 d后处死大鼠,测定股骨的几何尺寸、极惯性矩、抗扭截面模数、截面惯性矩、抗弯截面模数、骨矿密度和股骨的生物力学试验。
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BTW, China also executed a Japanese drug trafficker a couple years ago. Do you think the U.K.
顺便说一声,中国在两年前也处死了一个日本毒犯。
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Methods Male SD rats were selected, 5 for each group. Trichloroethylene at the doses of 1500 and 3000 mg/kg were poured into rats stomach through mouth, then they were killed after 48 hours.
选用雄性SD大鼠,每组5只,用1500和3000mg/kg的三氯乙烯经口灌胃染毒,48h处死动物。
- 推荐网络例句
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This one mode pays close attention to network credence foundation of the businessman very much.
这一模式非常关注商人的网络信用基础。
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Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.
扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。
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There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.
双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。