• 科学家们对此是这样解释的,母体生育每个男性胎儿时,会为男性胎儿产生抗原培育出增强免疫系统这种抗原很可能大脑的男性过程中发挥着重要作用

    Scientists explain that, with each male fetus, a mother develops an increased immunization to an antigen produced by the male fetuses, and this antigen likely plays a role in masculinizing the brain.

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  • 它们的运动能力吞噬处理抗原机能丧失

    Their movement tendency was disappeared and antigen procession function was lost.

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  • 方法:应用免疫检测乳腺癌及相应癌旁组织tlr4、增殖细胞核抗原(pcna)表达TUNEL检测组织中细胞的凋亡

    Methods: the expression of TLR4 and PCNA in cancer tissues and adjacent tissues were assessed by immunohistochemical method and the apoptosis was detected by the TUNEL method.

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  • 为了降低抗体反应获得满意的免疫原性,将模拟人卵巢癌抗原的抗独特型单链抗体人源

    In order to reduce the human anti mouse antibody response and obtain optimal antigenicity, anti idiotype single chain which mimicking ovarian cancer antigen has been humanized.

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  • 固相SARS抗原抗体并用ELISA检测噬菌体抗体结合SARS病毒特异性

    Antibodies against SARS virus were screened by biopanning with immobilized virus antigen. The binding specificity of phage antibody to SARS virus was detected by ELISA.

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  • 分析它的主要功能位点表明具有319的糖基位点完整抗原位点。

    Sequence analysis result indicated GP had a glycosylation site at position 319 and whole antigenic sites.

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  • 方法:采用免疫法检测9丙型肝炎患者外组织内hcv抗原肝组织内抗原表达进行对比研究。

    Methods: Immunohistochemical assay was used to determine the expression of HCV antigen in the kidneys, heart, pancreas, intestine and liver in 9 patients with viral hepatitis c.

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  • 方法免疫组SABC检测单克隆抗体,分别使用水煮微波法、高压法修复抗原,从中选出最佳修复方法

    Methods Check five kinds of antibody with immunohistochemistry SABC method and chose the best antigen retrieval method among poach method, microwave method and high pressure method respectively.

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  • 甲免疫法检查病毒分布表明,全身各器官均存在特异性病毒抗原,其中尤以脑、的病毒抗原量最多。

    Specific viral antigen were detected in all organs examined with highest titers in the brain, lung and kidney both by immunofluorescence and immunoperoxidase assays.

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  • 分别采用免疫组方法原位末端标记检测垂体前叶细胞增殖抗原表达凋亡情况

    The changes of the proliferating nuclear antigen expression and apoptosis of anterior pituitary cells were detected with immunohistochemistry and in situ end labeling method.

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  • 结果石蜡组织切片免疫组反应预处理,采用水浴抗原修复阳性表达为5 2 .6% ,片率为2 .0 % ;

    Results Prerteat organization chip, using the middle temperature water bath antigen repairing method, the positive expressing rate is 52.6% and the unfalling rate is 2.0%;

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  • 应用免疫方法检测增殖细胞核抗原P-选择表达

    The local expression of proliferating cell nuclear antigen(PCNA) and P-selectin were analyzed by immunohistochemical technique.

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  • 去糖基小麦PGIP不能的天然PGIP产生抗体发生免疫学反应,可能由于小麦PGIP中寡糖链为抗原决定部位。

    After deglycosylated, wheat PGTP could not interact with antibody produced by purified native PGtP from wheat. It is the glycans of wheat PGIP that probably fonn the epitope.

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  • 方法应用免疫101例大肠癌组织石蜡标本进行MAGE-3抗原表达测定。

    Method Immunohistochemical technique for MAGE-3 antigen was performed in paraffin embedded sections of 101 CRC specimens.

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  • 同时进行白细胞共同抗原CD34、CD 20免疫组观察。

    In addition, immunochemistry of CD34, CD20, and leukocyte common antigen was detected.

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  • 方法免疫组检测慢性HCV感染者卵巢输卵管组织内hcv抗原的表达及分布。

    Methods: the immunohistochemical method was applied to detect the antigen of HCV in ovary and oviduct.

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  • 方法通过TUNEL检测三类乳腺癌凋亡细胞数量分布比例差异,采用S-P免疫组法检测淋巴细胞CD57抗原表达强度差异。

    Methods The number of apoptosis cells were identified by TUNEL method and the expression intensity of antigen CD57 in lymph cells nearby the carcinoma was determined by S-P method.

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  • -干燥条件比较温和,微胶囊过程没有破坏灭活sars冠状病毒抗原

    The antigenicity of SARS virus was not destroyed in the encapsulation process because of the mild conditions of membrane emulsification-drying method in liquid.

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  • 结论枸橼缓冲液(PH6.0)微波抗原修复组织样本PV检测法是CD 117免疫表达较为理想检测方法

    Conclusions it is the ideal method of detection of CD117 antigen that CD117 antigen was retrieved by citric acid buffer (PH6.0) microwave antigen retrieval and detected by PV staining.

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  • 方法免疫检测了29结肠癌30溃疡性结肠炎28例正常人结肠组织PS 2和癌胚抗原(CEA)的表达

    Methods: PS2 and CEA protein expression in the tissues from 29 patients with colonic carcinoma, 30 ulcerative colitis and 28 normal control were measured by the immunohistochemical method.

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  • 目的探讨抗原系列修复后冰冻切片抗体应用石蜡切片免疫技术。

    Aim: to explore how to make the antibody which is originally applied to the frozen section be used for the paraffin section through a series of treatments of the tissue antigen recovery.

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  • 方法应用SP免疫组,检测P 21, P27等细胞周期依赖性激酶抑制剂增殖细胞核抗原(pcna)角膜上皮不同部位表达情况。

    METHODS: the expressions of CKI, P27, P21 and proliferating cell nuclear antigen (PCNA) were tested in different regions of corneal epithelium by SP immunohistochemistry.

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  • 方法应用免疫的方法(SP)观察了HLA -DR抗原15斑秃皮损中8正常头皮组织中的表达情况。

    Method: Immunohistochemical technology (sp method) was used to detect the HLA-DR antigens in scalp specimens from15 cases of AA and 8 normal controls.

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  • 免疫组检查脾细胞中STAT 5磷酸STAT 5抗原定位。用电泳迁移率变动分析(EMSA)测定STAT 5DNA探针的结合力

    The phosphorylation of STAT5 and its location were examined by double immunohistochemical staining and the binding of STAT5 with DNA was determined by electrophoretic mobility shift assay (EMSA).

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  • 应用放射免疫测定法,20胃肠患者进行血清抗原(CEA)测定,并应用免疫其中16组织中的CEA进行了检测。

    The serum CEA levels were measured by radioimmunoassay in 20 patients with primary gastrointestinal carcinoma. 16 cases were stained for CEA in tissue sections by immunohistochemical technique.

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  • 发明涉及人源人和嵌合RS7抗原结合蛋白以及结合蛋白在诊断治疗中的用途

    The invention further relates to humanized, human and chimeric RS7 antigen binding proteins, and the use of such binding proteins in diagnosis and therapy.

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  • 组织免疫染色原位杂交显示肾小球肾小管上皮细胞内存在VZV抗原转录产物rna

    VZV antigen and RNA transcript were found in glomerular and tubular cells by immunohistochemical staining and in situ hybridization of renal tissues, respectively.

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  • 许多病毒抗原都有现象,改变病毒对宿主的免疫逃避、病毒抗原免疫原性等。

    Many viral antigens are glycosylated, different glycosylation will influence the immunogenicity and immune evasion of virus.

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  • 目的:可溶性HLAA2 抗原复合物的体外折叠复性生物素

    AIM: To refold and biotinylate HLA A2 peptide complex in vitro .

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  • 方法:用人结肠癌细胞株lovo免疫小鼠间接细胞ELISA免疫的方法筛选抗结肠癌相关抗原的单抗。

    Methods: the mice were immunize with LOVO, and the mAb were screened by indirect cell ELISA and immunohistochemistry.

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