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   免疫定量 的翻译结果: 查询用时:0.387秒
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免疫定量
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  “免疫定量”译为未确定词的双语例句
     Carbohydrate antigen 19-9 (CA19-9), carbohydrate antigen 125 (CA125), carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP) were examined in enzyme immunometric assay;
     酶联免疫定量检测法检测糖链抗原19-9(CA19-9)、糖链原125(CA125)、癌胚抗原(CEA)及甲胎蛋白(AFP);
短句来源
     DS18B20 and Its Usage in Stability Temperature System of Chemiluminescent Fluorescence Immunoassay Detector
     DS18B20及其在化学荧光免疫定量检测仪恒温系统中的应用
短句来源
     Results The magnetic-bead ELISA gave a linear response in the dynamic range of 5- 1 000 μg/L, as compared to 5-200 μg/L by classic ELISA.
     结果 磁珠酶免疫定量检测方法用于人血清Mb定量检测范围可从常 规板式ELISA的5~200μg/L扩展到5~1000μg/L。
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     A Study of Diagnosis of Liver Diseases by Immunologic Quantitative Assay of Apo-B in Serum
     血清APo-B的免疫定量对肝病诊断意义的探讨
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     A STUDY ON QUANTITATION OF HUMAN SERUM APOLIPOPROTEIN B_(100) BY ENZYME-LINKED IMMUNOSORBENT ASSAY
     酶联免疫定量检测人血清载脂蛋白B_(100)的研究
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  相似匹配句对
     System Design of the Chemiluminescent Fluorescence Immunoassay Detector
     化学发光免疫定量测量仪的系统设计
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     pylori quantitative culture of the gastric mucosa another 4 weeks later.
     pylori定量培养 ,对照观察免疫效果。
短句来源
     Immunization Update
     当代免疫
短句来源
     The Immune Programming
     免疫规划
短句来源
     Electronic weigher for quantified packing
     定量包装电子秤
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  immunoquantitation
These findings may reflect different pollution histories of the sites, and indicate the applicability of biochemical effect indices (i.e., EROD and P450 1A1 immunoquantitation) to monitoring studies.
      
Among these, CD34 immunoquantitation allows determination of the degree of vascular proliferation (angiogenesis), whereas VCAM-1 immunoquantitation allows evaluation of the degree of endothelial activity and is strong evidence of inflammation.
      
Immunoquantitation of some cytochrome P-450 isozymes in liver microsomes from streptozotocin-diabetic rats
      
First, the immunoquantitation of salivary components has been generally restricted to the major salivary gland secretions.
      
Immunoquantitation of CYP1A1 expression in individual rats is shown in Figure 2.
      


(1) Experiments confirm that the treatment of BSA with NBS in urea-acetate buffer of pH 4.1-4.2 results in the splitting of the peptide chain specifically at tryptophenyl bonds, and that the new N-terminal amino acids are serine and glycine.(2) The molecules of BSA are found to form aggregates partly after NBS treatment as shown by increase in both molecular weight (from 65,000 to 110,000) and intrinsic viscosity (from 0.041 to 0.076). Electrophoretic pattern of the NBS treated sample shows the appearance of...

(1) Experiments confirm that the treatment of BSA with NBS in urea-acetate buffer of pH 4.1-4.2 results in the splitting of the peptide chain specifically at tryptophenyl bonds, and that the new N-terminal amino acids are serine and glycine.(2) The molecules of BSA are found to form aggregates partly after NBS treatment as shown by increase in both molecular weight (from 65,000 to 110,000) and intrinsic viscosity (from 0.041 to 0.076). Electrophoretic pattern of the NBS treated sample shows the appearance of a new peak.(3) No significant change is shown in specific optical rotation, indicating the helical content of the BSA molecule remains unaltered.(4) The agar diffusion and quantitative precipitin reaction show that the antigenicity of BSA decreases considerably after NBS treatment.

(1)牛血清清蛋白在pH=4.1—4.2的醋酸-脲缓冲液中经15moles/mole BSA的NBS处理后,色氨酸肽键处断裂,出现新N-末端氨基酸,用叔戊醇及1.6M磷酸系统双相层析证实分别为丝氨酸及甘氨酸。(2)NBS处理后之BSA分子量由正常65,000增加到110,000。特性粘度由正常0.041上升至0.076,说明分子有部分聚合现象,在电泳图谱上出现一个新的峰。(3)BSA经NBS处理后此旋光度无变化,说明螺旋程度未发生明显的改变。(4)琼脂扩散及免疫定量实验结果显示NBS处理后BSA的抗原性减弱。

This paper is undertaken to establish a rapid radioimmunoassay method, namely an improved quantitative radio-countercurrent-immunoelectrophoresis. Substances with various moleoular weights and charges were chosen: insulin, human serum albumin, human fetal alpha-fetoprotein and the surface antigen of hepatitis B virus. Trial-assays of the above antigens were carried out repeatedly by the improved method. The whole procedure can be completed within 3~5 hrs for Ins, HSA and AFP and 6~7 hrs for HBsAg respectively....

This paper is undertaken to establish a rapid radioimmunoassay method, namely an improved quantitative radio-countercurrent-immunoelectrophoresis. Substances with various moleoular weights and charges were chosen: insulin, human serum albumin, human fetal alpha-fetoprotein and the surface antigen of hepatitis B virus. Trial-assays of the above antigens were carried out repeatedly by the improved method. The whole procedure can be completed within 3~5 hrs for Ins, HSA and AFP and 6~7 hrs for HBsAg respectively. It has been shown that the improved method possesses the advantages of high sensitivity and accuracy, extreme simplioity and rapidity, as well as satisfactory reproducibility. Therefore it is expected to be widely used in the trace amount estimations of various antigens migrating from the cathode towards the anode including small molecules, macremolecules, as well as virus particles.

改进后的放射对流免疫定量电泳不仅具有简易、快速和灵敏度高等优点,而且重复性好。本文选用胰岛素、人血清白蛋白、人胎儿AFP和HBsAg四种抗原-抗体系统对这一技术进行了考验,均获得了满意的结果。对HBsAg的定量测定只需6~7小时,另三种抗原需时更短,约3~5小时。因此认为这一技术有可能发展成为适合临床、科研需要的快速、精确的超微量定量手段。

This paper is undertaken to establish a rapid radioimmunoassay method,namelyan improved quantitative radio-countercurrent-immunceleotrophoresis.Substanceswith various molecular weights and charges were chosen:insulin,human serumalbumin,human fetal alpha-fetoprotein and the surface antigen of hepatitis B virus.Trial-assays of the above antigens were carried out repeatedly by the improvedmethod.The whole procedure can be completed within 3~5 hrs for Ins,HSA andAFP and 6~7 hrs for HBsAg respectively.It has been...

This paper is undertaken to establish a rapid radioimmunoassay method,namelyan improved quantitative radio-countercurrent-immunceleotrophoresis.Substanceswith various molecular weights and charges were chosen:insulin,human serumalbumin,human fetal alpha-fetoprotein and the surface antigen of hepatitis B virus.Trial-assays of the above antigens were carried out repeatedly by the improvedmethod.The whole procedure can be completed within 3~5 hrs for Ins,HSA andAFP and 6~7 hrs for HBsAg respectively.It has been shown that the improvedmethod possesses the advantages of high sensitivity and accuracy,extreme simplicityand rapidity,as well as satisfactory reproducibility.Therefore it is expected to bewidely used in the trace amount estimations of various antigens migrating from thecathode towards the anode including small molecules,macromolecules,as well asvirus particles.

改进后的放射对流免疫定量电泳不仅具有简易、快速和灵敏度高等优点,而且重复性好。本文选用胰岛素、人血清白蛋白、人胎儿AFP 和HBsAg 四种抗原-抗体系统对这一技术进行了考验,均获得了满意的结果。对HBsAg 的定量测定只需6~7小时,另三种抗原需时更短,约3~5小时。因此认为这一技术有可能发展成为适合临床、科研需要的快速、精确的超微量定量手段。

 
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