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国际参考制剂
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  international reference preparation
    The relative potency of national TSH standard to 2~(nd) international reference preparation was 0.942.However,there was some difference between each immunoassay methods.
    TSH国家标准品与第2次国际参考制剂的相对效价为0.942。 然而,在不同的免疫分析方法之间存在一定差异。
短句来源
    Precision of duplicate showed a relative potency of 0.84~1.08 for 2~(nd) international reference preparation of TSH and that of 0.82~1.18 for TSH 81/565.Results of accelerated thermal degradation test at 4 ℃ conformed to the trend of immunoactivity change described in WHO report.
    双份样品精密性测定:TSH第2次国际参考制剂双份样品之间的相对效价为0.84~1.08,TSH 81/565双份样品之间的相对效价为0.82~1.18。 +4℃热加速降解样品测定结果符合WHO报告中所述的免疫活性变化趋势。
短句来源
    International Collaborative Study on the Proposed 3~(rd) International Reference Preparation of TSH for Immunoassay
    免疫测定用人垂体促甲状腺激素第三次国际参考制剂国际协作标定
短句来源
    The final product, then identified by SDS gel electrophoresis, agar diffusion, immuno electrophoresis and radioimmunoassay. It was demonstrated that the present CEA has a molecular weight of 200,000, its immunoactivity was as same as the French CEA and the International reference preparation, and dose calibration was found to be 100ng correspodence to 1 international unit.
    所得产品用 SDS凝胶电泳、琼脂扩散、免疫电泳和放射免疫分析法等鉴定,分子量为200,000,免疫活性与法国提供的癌胚抗原和国际参考制剂相一致,剂量校对100ng=1国际单位。
短句来源
  “国际参考制剂”译为未确定词的双语例句
    The serum pool has been subaliquoted (in 0.5ml/ ampule), lyphilized and stored at 4℃-The total IgE content was calibrated with WHO IgE Reference Preparation 69/204 (10,948IU/ml) by the paper radioimmunosorbent test (PRIST) technique.
    参照 WHO code 69/204(10,948IU/ml)IgE 国际参考制剂,以纸片放射免疫吸附试验,用四剂量法标定其中总IgE的含量。 标定结果是2,680IU/ml,并对血清分装量进行测定,各安瓿间血清湿重误差 ±2.12%;
短句来源
    Immunological potencies of TSH 81/565(candidate 3~(rd) TSH IRP),TSH 81/615,TSH 81/502 and TSH national standard were assayed respectively by CLIA,ELISA,RIA and IRMA kits with the 2~(nd) international TSH reference preparation as control in an international collaborative study.
    本文报告了在国际协作研究中,以TSH第2次国际参考制剂为对照品,用化学发光免疫分析、酶联免疫分析、放射免疫分析和免疫放射量度分析试剂盒测定TSH 81/565(候选的TSH第3次国际参考制剂)、TSH 81/615和TSH 81/502以及TSH国家标准品的免疫效价。
短句来源
    The potency of CEA working standard, in terms of present standard of CEA RIA and IRMA kits made by Chinese manufacturers and in terms of 1st IRP CEA HUMAN 73/601 supplied by WHO, has been determined.
    分装、冻干。 以国产CEARIA和CEAIRMA药盒现行标准品为对照品 ,标定工作标准品效价 ,并与国际参考制剂 1stIRPCEAHUMAN 73/ 6 0 1进行对照实验。
短句来源
    Test of parallelism of dose-response curve for the working standard to that for 1st IRP CEA HUMAN 73/601 has been passed. CEA working standard is suitable to the kits standard for CEA radioimmunoassay and immunoradiometric assay.
    ,工作标准品与国际参考制剂的剂量 -反应曲线不显著偏离平行。 CEA工作标准品与国际参考制剂 1stIRPCEA 73/ 6 0 1在免疫学反应中是同质的 ,可以作为实验室间对照品使用
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  international reference preparation
It is proposed that an International Reference Preparation for free light chains is established.
      
Calibration can be improved by direct comparison of a POC system against an established international reference preparation method.
      
All t-PA concentrations are reported ininternational units by comparison with the International Reference Preparation for t-PA.
      
One of these candidate preparations will later be selected to replace the dwindling stocks of the current International Reference Preparation.
      
Spe cific fibrinolytic activities were measured on fibrin plates26 by comparison with the International Reference Preparation for Urokinase.
      
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The Procedures of isolation and purification of the carcinoembryonic antigen from hepatic metastatic tissue of colonic carcinoma were presented. The crude CEA obtained by the extraction of hepatic homogenate with perchloric acid and ethyl alcohol. Purification were carried out by sepharose 4B, Sephadex G200 gel filtration and Con A sepharose affinity chromatography. The final product, then identified by SDS gel electrophoresis, agar diffusion, immuno electrophoresis and radioimmunoassay. It was demonstrated...

The Procedures of isolation and purification of the carcinoembryonic antigen from hepatic metastatic tissue of colonic carcinoma were presented. The crude CEA obtained by the extraction of hepatic homogenate with perchloric acid and ethyl alcohol. Purification were carried out by sepharose 4B, Sephadex G200 gel filtration and Con A sepharose affinity chromatography. The final product, then identified by SDS gel electrophoresis, agar diffusion, immuno electrophoresis and radioimmunoassay. It was demonstrated that the present CEA has a molecular weight of 200,000, its immunoactivity was as same as the French CEA and the International reference preparation, and dose calibration was found to be 100ng correspodence to 1 international unit.

本文报道从结肠癌肝转移灶中提取和纯化癌胚抗原的步骤。肝转移组织制成匀浆,用过氯酸和乙醇提取得到癌胚抗原的粗制品,经sepharose 4B和sephadex G-200 凝胶过滤,Con A琼脂糖亲和层析进行纯化。所得产品用 SDS凝胶电泳、琼脂扩散、免疫电泳和放射免疫分析法等鉴定,分子量为200,000,免疫活性与法国提供的癌胚抗原和国际参考制剂相一致,剂量校对100ng=1国际单位。

Human sera comiming high IgE level were screened by single radial immunodif-fusion and reversed hemagglutination methods and collected for the preparation of human IgE working standard. 2,300ml high IgE sera from 17 human donors were mixed with 300ml sera from 612 normal adults. The serum pool has been subaliquoted (in 0.5ml/ ampule), lyphilized and stored at 4℃-The total IgE content was calibrated with WHO IgE Reference Preparation 69/204 (10,948IU/ml) by the paper radioimmunosorbent test (PRIST) technique....

Human sera comiming high IgE level were screened by single radial immunodif-fusion and reversed hemagglutination methods and collected for the preparation of human IgE working standard. 2,300ml high IgE sera from 17 human donors were mixed with 300ml sera from 612 normal adults. The serum pool has been subaliquoted (in 0.5ml/ ampule), lyphilized and stored at 4℃-The total IgE content was calibrated with WHO IgE Reference Preparation 69/204 (10,948IU/ml) by the paper radioimmunosorbent test (PRIST) technique. The total IgE content of this human IgE working standard (code 861A) is 2680 IU/ml and free from hepatitis B surface antigen.This method not only ensures standardization of IgE but also is suitable for calibration of other immunoglobulins.

本工作用单向免疫扩散法和反向被动血凝法筛选并收集高IgE健康人混合血清,制备供体外测定用的IgE作标准血清。混合血清无乙型肝炎表面抗原,定量分装为每安瓿0.5ml,经冷冻干燥后,4℃保存。参照 WHO code 69/204(10,948IU/ml)IgE 国际参考制剂,以纸片放射免疫吸附试验,用四剂量法标定其中总IgE的含量。标定结果是2,680IU/ml,并对血清分装量进行测定,各安瓿间血清湿重误差 ±2.12%;血清干重误差 ±1.81%;冻干血清溶解时间范围 1分 5秒~1分16秒。本次制备的IgE工作标准血清批号为861A。本法不仅保证标准化,且可用于其他类免疫球蛋白的标定,有普遍意义。

 
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