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syngenic相关的网络例句

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与 syngenic 相关的网络例句 [注:此内容来源于网络,仅供参考]

Syngenic monoclonal anti-idiotypic antibodies (MAb_2s), AFE_8Id_(16-6) and ALA_(15-6)Id, were raised against an idiotype on a protective monoclonal antibody with specificity for NDV.

用AFE_8Id_(16-6)和ALA_(15-6)Id两株新城疫病毒的抗独特型单抗(MAb_2)分别免疫接种一组(18只)无HI抗体鸡,并以一组(7只)Lasota苗常规免疫鸡和一组(12只)不免疫的易感鸡分别作为免疫阳性和阴性对照。

The immuno-protective activity of the vaccine was determined by CTL induction and tumor growth inhibition in vaccine-immunized syngenic mice.

以重组质粒免疫C5 7BL/ 6小鼠,检测诱发的特异性CTL活性;将免疫后的小鼠用TC - 1肿瘤细胞攻击,观察免疫保护效果。

Methods:The effects of N-CWS on bladder carcinoma and on the activities of interleukin-2(IL-2) and NK cell were studied in syngenic mice bearing bladder carcinoma.

膀胱癌荷瘤鼠注射N-CWS,观察N-CWS的抑瘤效果及N-CWS对白细胞介素2(IL-2)水平和自然杀伤细胞活性的影响。

METHODS: Two groups of rats [allograft group and syngenic graft group] underwent limbal transplantation and healthy rats were taken as normal controls. The expression of RANTES and MCP 1 mRNA was detected by quantitative competitive RT PCR at post operative days 1, 3, 7, 11, 14, 21 and 30 and rejections were observed.

将大鼠随机分为同种异体移植组、自体移植组,并以健康大鼠作为正常对照组,用定量竞争性RT PCR的方法,在术后1, 4, 7, 11, 14, 21和30 d分别检测各组大鼠RANTES和MCP 1 mRNA的含量,并观察大鼠眼表变化,判断排斥反应的发生。

The recipient Balb/c mice were randomly divided into four groups: intrathymic injection group, syngenic transplantation group, allogenic transplantation group and immunosuppressant drug group.

将受体鼠Balb/c随机分为4组:胸腺内注射组、同系同基因移植组、异体神经移植组、免疫抑制剂组。

Establishment of the murine tumor cell lines expressing human M-CSFR-m-M-CSF fusion gene: The syngenic BALB/c mouse myeloma derived cell line SP2/0 was transfected with pF. Four stable expression cell lines were obtained after selection using G418 and cloning by limiting dilution.

表达人M-CSFR-m-M-CSF的小鼠肿瘤细胞系的建立:以pF转染小鼠骨髓瘤细胞系SP2/0,应用G418筛选,经克隆化培养建立了四株稳定表达人M-CSFR-m-M-CSF的SP2/0细胞系。

Methods:The syngenic mice were immunized with parental B16 tumor cells and B16.B fusing cells.Then,SPLs of immunized mice were co-cultured in vitro with parental B16 cells,the proliferation of SPLs and the secretion of certain cytokines were assayed.

分别取亲本B16黑色素瘤和融合瘤细胞B16.B主动免疫同系小鼠,观察免疫小鼠脾脏淋巴细胞对亲本瘤细胞体外再刺激的反应能力。

METHODS: Orthotopic liver transplantation was used in this study. Group Ⅰ: syngenic control (Wistar-to-Wistar); Group Ⅱ: acute rejection (SD-to-Wistar); Group Ⅲ: thymus inoculation of SD rat LSA day 7 before transplantation.

实验为同种肝移植:Ⅰ组为Wistar→Wistar同基因对照组;Ⅱ组为SD→Wistar急性排斥组;Ⅲ组为SD→Wistar术前1周供体肝特异性蛋白受体胸腺内注射处理组。

After being induced to differentiate in vitro, cells with various morphologies showed β-gal activity, including nerve cells, neuroglial cells, epithelial cells. We also detected β-gal activity in a wide variety of tissue elements in solid tumors made by injecting the MC15 and MA34 cells into syngenic mice. Then we produced chimeric embryos by injecting the MC15 cells into Kunming blastocysts and recovering the embryos at various developmental stages.

SiCMVIE(Simian Cytomegalovirus Immediately Early)启动子是一个强启动子,本文首次将SCMVIE启动子应用到ES细胞途径上制作嵌合鼠,并通过lacZ基因在ES细胞和早期嵌合胚胎中的表达,表明该启动子是一个能在小鼠多数组织表达的启动子,这与1993年Peppel等人用原核显微注射法获得的转基因小鼠上所得的有关结果是基本上是一致的。

Methods:Human CD80 cDNA was transfected into B16 melanoma cells by lipofectin-mediated gene transfer before the expansion of tumor cells were tested by MTT method in vitro;C57BL/6 mice were inculated subcutaneously either mock-transfected B16 cells (B16-neo)or CD80-transfected B16 cells (B16-CD80),then the latency,survival times and tumor mass growth were investigated.The lymphocytes were examined for both proliferation indices and specific cytotoxic activity by MTT method and improved LDH-releasing method,after syngenic Mixed Lymphocyte tumor cultures.

通过脂质体介导将CD80基因导入小鼠黑色素瘤B16细胞后,利用SABC法检测CD80的表达;MTT法测定肿瘤细胞体外增殖能力;将肿瘤细胞接种至同源小鼠皮下后观察成瘤期、荷瘤小鼠存活期及肿瘤结节生长速度;在同源淋巴细胞肿瘤细胞混合培养后,通过测定淋巴细胞增殖指数和CTL杀伤活性检测肿瘤细胞的免疫原性。

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