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双语推荐:免疫电镜

采用氯化铯平衡密度梯度离心获得较为纯净的病毒粒子后,经过免疫电镜技术(液相免疫电镜法和免疫胶体金标记法)对P1病毒进行了观察鉴定。结果表明,P1病毒呈球形、无囊膜、直径约为25 nm。
The results of porcine circovirus-like agent P1 morphology were reported here .Relatively pure viral particles were obtained by CsCl equilibrium density-gradient centrifugation ,and then detected by immune electron microscopy ( Both liquid phase immune electron microscopy and immunogold labeling electron microscopy ) .The re-sults showed that P1 is spherical in shape ,non-enveloped and about 25 nm in diameter.

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免疫胶体金技术是一种新型固相标记免疫检测技术,因其独特的性质在许多领域得到广泛应用和快速发展。简述了免疫胶体金技术在电镜、光快速检测诊断中的发展以及在生物医学、免疫组织化学和细胞生物学等领域的研究和应用。未来免疫胶体金技术在提高胶体金制备质量的同时将实现定量和多元化检测。
Immune colloidal gold technique is a new kind of solid phase marked immune detection technology,it is widely applied in many fields and developed rapidly owe to its unique characteristics. The research and application of the immune colloidal gold technique in the rapid diagnosis with electron microscope,light microscope,and the field of biomedical,immunohistochemical and cell biology were briefly discussed. In the future,the technique of immune colloidal gold will improve the quality of colloid gold and achieve quantitative and diversity detection at the same time.

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探究2型猪链球菌(S.suis2)强毒株05ZYH33的srtF基因簇编码的菌毛结构亚蛋白SSU0473的细菌定位及其免疫保护效能。方法:原核表达截短的SSU0473(tSSU0473),并以亲和层析法纯化目的蛋白,Western印迹检测tSSU0473蛋白的免疫原性,ELISA法检测多抗血清的效价及IgG亚型,小鼠试验测试重组蛋白的免疫保护效能,免疫电镜观测tSSU0473蛋白的细菌定位。结果:在原核系统中表达了tSSU0473蛋白;ELISA结果显示重组蛋白能够刺激小鼠产生高效价的免疫抗体;动物试验表明tSSU0473蛋白免疫小鼠可抵御致死剂量病原体的攻击,显示出较好的免疫保护作用;免疫电镜检测显示tSSU0473蛋白定位于细菌表面。结论:菌毛亚蛋白tSSU0473是S.suis2膜表面蛋白,具有良好的免疫原性和免疫保护性,可作为S.suis2亚单位疫苗的候选分子。研究结果为系统揭示S.suis2的菌毛生物学结构与功能奠定了基础。
Objective: To elucidate the inmmunoprotection of pilus subunit SSU0473 encoded by the srtF pilus is-land in the Chinese strain 05ZYH33 of Streptococcus suis serotype 2(S.suis2). Methods: The truncated protein tSSU0473 was expressed in prokaryotic cells and was purified by affinity chromatography. Then recombinant pro-tein was analyzed by Western blotting, and the anti-SSU0473 serum was prepared by immunizing mice with recom-binant tSSU0473 protein and analyzed by ELISA. The location site of tSSU0447 protein in bacterium was detected by immune electron microscopy. Results: The tSSU0473 protein was expressed successfully in prokaryotic system. The high titer of the serum was obtained, ELISA result indicated that the recombinant protein can react with mice anti-SSU0473 serum. Animal test showed that vaccinating mice with recombinant tSSU0473 protein conferred a significant protection. The tSSU0473 protein was detected on bacterial surface by immune electron microscopy. Conclusion: Protein

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探讨毛细胞白血病(HCL)特征性诊断及鉴别诊断方法。方法:对4例HCL患者的临床特征及骨髓病理、组织细胞化学、白血病免疫分型、电镜等实验室检查结果进行分析。结果与结论:骨髓病理、组织细胞化学、白血病免疫分型、电镜在HCL的诊断中具有重要意义,HCL的鉴别诊断须结合患者临床特征及实验室检查。
Objective: To investigate characteristic diagnosis and differential diagnosis methods of hairy cell leukemia ( HCL) .Methods:Clinical features and bone marrow pathology , tissue chemistry , leukemia immunoph-enotyping , electron microscopy and other laboratory findings of four patients with HCL were analyzed .Results and Conclusion:Bone marrow pathology , histochemical and cytochemical , immunophenotyping of leukemia , electro microscopy play an important role in the diagnosis of HCL .The differential diagnosis of HCL should combine the clinical characteristic of and laboratory tests .

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通过免疫亲和层析对类猪圆环病毒因子P1纯化进行了研究。采用环氧活化及NHS活化的琼脂糖凝胶,与兔抗P1表位肽抗体偶联,对P1进行了免疫亲和吸附,通过电镜技术证实获得了纯化病毒。结果表明,免疫亲和层析是有效的P1病毒纯化方法。
This study deals mainly with porcine circovirus-like agnet P1 antigen purified by immuno-affinity chromatography .The purified P1 virus, which came from elution buffers from adsorption column coupled anti-P1 epitope-containing peptide antibody to either Epoxy-activated agarose or NHS-activated agarose , was confirmed by transmission electron microscopic observations .The study suggests that purified P 1 antigen by immuno-affinity chro-matography is an effective way .

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目的:建立脑组织生长锥提取的方法。方法:采用梯度蔗糖离心的方法提取生长锥,透射电镜和扫描电镜观察分离物的形态,免疫荧光和免疫印迹检测GAP.43的表达。结果:梯度浓度蔗糖离心把脑组织悬液分离为3层,上层密度小,浓度位于上清至0.75mol/L蔗糖之间,中层密度较大,浓度位于0.75~1.00mol/L蔗糖之间,下层密度最大,浓度位于1.00—2.66mol/L蔗糖之间;透射电镜见上层分离物为大量着色浅的空泡状结构,颗粒大小较均匀,中、下层分离物为大量着色深的致密颗粒及不规则形态的细胞碎片,颗粒大小不均匀;扫描电镜见分离物颗粒均为白色、大小不一、形状不规则的颗粒,上层较中、下层颗粒体积大;免疫荧光及免疫印迹证实分离物中均有大量GAP-43表达,上层分离物几乎无GFAP表达,中、下层有少量GFAP表达。结论:梯度蔗糖离心的方法可以依据颗粒的大小分离脑组织,分离物最上层内的组分为生长锥。
Aim:To establish a method to extract growth cone from brain tissue.Methods:Using gra-dient sucrose centrifugation to extract growth cone,transmission electron microscopy and scanning elec-tron microscopy to observe the morphology of the isolate,immunofluorescence and immunoblotting to de-tect the express of GAP-43 protein.Results:Gradient sucrose centrifugation isolated the brain tissue into three layers,the upper layer with low density,located between the supernatant and 0.75 sucrose,the middle layer with higher density sucrose,located between 0.75 to 1.0 mmol/L,the lower layer with the highest density sucrose,located between 1.00 to 2.66 mmol/L.Observed by transmission electron mi-croscopy,the results showed that the upper layer contained a number of shallow-coloured vacuoles,and the particle size was uniform.The middle and lower layer contained a number of deep-coloured dense particles and irregular shaped cell debris,and the particle size was not uniform.The scanning electron micro

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目的 研究登革2型病毒(Dengue virus type 2,DENV-2)病毒样颗粒(virus-Like particles,VLPs)的免疫原性.方法 利用已构建的DENV-2 ZS01/01株病毒样颗粒的表达质粒转染293T细胞,对分泌型VLPs进行大量培养并通过蔗糖密度梯度离心法对其进行纯化.纯化的VLPs经Western Blot及透射电镜观察等方法鉴定后免疫BALB/c小鼠.利用ELISA及中和试验等方法对体液免疫反应进行检测,ELISPOT法测定细胞免疫水平.结果 登革2型病毒样颗粒表达质粒转染哺乳动物细胞所得上清经蔗糖密度梯度离心后,电镜下可观察到类似于天然登革病毒的大小在45~55nm之间的病毒样颗粒.体液及细胞免疫检测结果显示登革2型VLPs可以刺激小鼠产生较高水平的登革E蛋白特异性抗体及一定水平的中和抗体,免疫小鼠脾淋巴细胞经体外刺激后IFN-γ水平显著升高.结论 登革2型病毒病毒样颗粒免疫BALB/c小鼠后可引起一定水平的细胞免疫及体液免疫反应,该研究结果为四价登革病毒样颗粒疫苗的研制奠定了基础.
Objective To study the immunogenicity of virus-like particles (VLPs) of dengue virus type 2 (DENV-2) ZS01/01 strain.Methods Secreted VLPs of DENV-2 ZS01/01 strain were purified by ultracentrifugation from 293T cells transfected with plasmid which was established previously in our lab.After identified by Western Blot analysis and transmission electron microscope (TEM),the immunogenicity of DENV-2 VLPs was evaluated in BALB/c mice.Humoral immune responses were identified by ELISA and CPE-based neutralization analysis while cellular immune responses were detected by ELISPOT.Results The analysis of humoral immune responses revealed that DENV-2 VLPs induced high levels of dengue rEIII-specific IgG antibodies and elicited homotypic neutralizing antibodies against DENV-2 NGC strain.Furthermore,spleen cells from mice vaccinated with DENV-2 VLPs and virions produced comparable levels of IFN-γ.Conclusion Monovalent DENV-2 VLPs produced by mammalian cells were capable to induce dengue-

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通过免疫电镜技术的应用,探讨微波辐射致大鼠海马突触结构损伤的机制。方法:采用30mW/cm2微波辐射Wistar大鼠,通过电镜观察辐射后6h海马突触结构改变;采用不同实验条件摸索胶体金标记的免疫电镜染色方法,并检测磷酸化突触素I和囊泡氨基酸递质转运体的改变。结果:30mW/cm2微波辐射后大鼠海马突触前囊泡堆积,活性区延长、突触后致密物增加、突触曲率增加,GABA囊泡转运体和磷酸化突触素I(Ser-553)在海马堆积囊泡中表达增加。结论:胶体金标记的免疫电镜染色操作过程中,固定液中戊二醛浓度和处理时间对其结果影响至关重要;微波辐射可引起突触结构损伤,Ser-553位点突触素I磷酸化参与微波辐射所致GABA能囊泡的堆积。
Objective:To investigate the mechanism of synaptic structure injury after microwave radia-tion in hippocampus of rats by application of immunoelectron microscopy .Methods:Wistar rats were ex-posed to microwave radiation .Electron telescope was used to study the change of the synaptic structure at 6h after radiation .The different experiment conditions were used in colloidal gold immunoelectron micros-copy and to study the change of phosphorylated synapsin I and vesicular amino acids neurotransmitter transporters .Results:The average power density which was set at 30mW/cm2 ,0 .1% glutaraldehyde in fixative fluid and short time of sucrose dehydration were better for maintenance of ultraculture and anti-gens activity .It resulted in deposits of synapse vesicle ,elongation of active zone ,the increase of thickness of postsynaptic density and perforation of synapse ;the expressions of vesicular GABA transporter and phosphorylation of synapsin I at Ser-553 were increased in cumulated synapse

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目的 观察猴脑边缘区甲硫氨酸-脑啡肽(MET-ENK)阳性免疫反应神经终末突触的超微结构,为进一步探索其学习记忆功能提供超微结构基础. 方法 选取健康成年雄性恒河猴6只,常规灌注固定和取脑,冰冻切片后行免疫组织化学染色检测纹状体MET-ENK的表达,取边缘区内免疫组化染色阳性反应区进行超微切片,电镜下观察边缘区MET-ENK阳性反应神经终末突触的超微结构. 结果 免疫组织化学染色显示在壳核和苍白球之间有一条密集排列的MET-ENK免疫反应阳性细胞带,即纹状体边缘区;电镜下可见边缘区神经元为长梭形或纺锤形,细胞器较少.MET-ENK阳性反应神经终末突触主要有5个类型:轴-树突触、轴-棘突触、轴-体突触、轴-轴突触以及多种类型的复合型突触. 结论 猴脑纹状体边缘区MET-ENK阳性免疫反应神经终末突触结构具有多样性和复杂性,明显不同于纹状体其他部分.
Objective Marginal division (MrD) of striatum is a universal structure in the mammalian brain,and it plays an critical role in learning and memory.In the present study,we try to investigate the synaptic ultrastructure of Methionine enkephalin (MET-ENK) immunoreacted fibers connected with neurons in the marginal division of the striatum in the monkey brains to explore the ultrastructural basis of the mechanism of learning and memory function in MrD.Methods Six male monkeys (macaque) were perfused with paraformaldehyde through heart to fix the brain and the brains were sectioned by a cryostat.Sections of the brains were performed immunohistochemical staining to detect the MET-ENK expression in the stfiatum; the areas with positive immumohistochemical staining was performed ultrastructural observation for morphological characteristics of the MET-ENK synapses in the MrD.Results Immunohistochemistry staining showed a dense arrangement of MET-ENK immunoreactive cells between the putamen and

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目的探讨原发性膜性肾病合并IgA肾病的临床、病理特点及诊断要点。方法分析我院确诊的2例膜性肾病合并IgA肾病病例的临床和病理资料,并进行文献复习。结果两例均为男性,年龄分别为17岁、73岁。例1表现为肾病综合征伴下血尿;例2以蛋白尿伴下血尿发病,9年后出现肾病综合征。两例血压及肾功能均正常。肾脏病理:光下均见肾小球基底膜空泡变性和增厚,系膜细胞和基质增生;免疫荧光见IgG和C3颗粒样沿肾小球毛细血管壁沉积,IgA团块状在系膜区沉积;电镜下均见肾小球上皮细胞下多数团块状子致密物沉积,系膜区见团块状子致密物沉积,上皮细胞足突广泛融合。两例均予激素治疗缓解,随访29~41个月肾功能正常。结论原发性膜性肾病合并IgA肾病临床表现无特异性,病理上兼具有膜性肾病和IgA肾病的病理特点。免疫荧光和电镜免疫电镜在诊断中具有重要意义。
Objective To describe the clinical and pathological characteristics and diagnosis of membranous nephropathy combined with IgA nephropathy. Methods Two patients were confirmed to have idiopathic membranous nephropathy and IgA nephropathy in our hospital. We analyzed the clinical and pathological data and reviewed literature. Results Two patients were all male, 17 and 73 years old. One patient had nephrotic syndrome and microscopic hematuria, The other had proteinuria and microscopic hematuria initially, after 9 years performed nephrotic syndrome. Blood pressure and renal function of two patients were normal. The pathological characteristics included vacuolation and thickening of the glomerular basement membrane, mesangial cells and matrix hyperplasia. And IgA deposit in mesangium, IgG and C3 deposit in subepithelial site mainly. Lumpy electron dense deposited in subepithelial and mesangial area and foot processes fusion under electron microscopy. Two cases were remission after hormone t

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