因此建立胶体金免疫层析快速筛选法。
Therefore we establish the gold immunochromatography assay (GICA) screening method.
目的建立上转磷光免疫层析技术快速定量检测炭疽芽孢。
Objective To develop a method for fast and quantitive detection of anthrax spore.
方法：采用免疫层析法和ELISA法检测血清中特异性抗体。
Methods; the specific antibody in the serum were detected by immunochromatography and ELISA.
目的探讨免疫层析法检测结核抗体在肺结核诊断中的应用价值。
Objective to investigate the application value of immunochromatography for the detection of anti-tuberculosis antibody in diagnosing pulmonary tuberculosis.
介绍了金免疫层析试剂及具有代表性的定量测试装置的工作原理。
The principle of GICA strip and its representative quantitative detection system were introduced.
将模糊控制理论应用于PSA金免疫层析系统的基值自动调零部分。
Methods Fuzzy control theory was applied to automatic zero setting of the PSA quantitative detection system.
方法：应用竞争抑制免疫层析原理，研制磺胺二甲基嘧啶胶体金试纸条。
Methods: the colloidal gold strip for specific sulfadimidine was developed successfully on the basis of competitive inhibition immunochromatography mechanism.
方法将模糊控制理论应用于PSA金免疫层析系统的基值自动调零部分。
Methods Fuzzy control theory was applied to automatic zero setting of the PSA quantitative detection system.
结果基值自动调零在金免疫层析PSA测定系统的实现，提高了仪器的精密度。
Results The automatic zero setting increased the precision of the PSA quantitative detection system.
本实验建立了检测鹅副黏病毒的快速夹心胶体金免疫层析测试试纸条（ICS）。
In this study , We establish a rapid and sensitive sandwich immunochromatographic strip(ICS) for goose paramyxovirus (GPMV) detection.
研究金免疫层析定量智能检测仪器的光电信号检测、数据采集与传输等部分的设计。
To study the detailed designs for the intelligent quantitative test instrument, such as the department of photoelectric signal detection, data collection, data transmission, and so on.
其原理是利用抗原抗体的特异结合反应和免疫层析技术，在试纸上出现特定的显色结果。
The theory is to utilize the specific binding reaction and immunochromatography technique of antigen antibody, with specific chromogenic results on test paper.
血清样品检测显示，SARS抗体的胶体金和UCP免疫层析方法均有较好的特异性和敏感性。
The detection of SARS antibodies by colloid gold immunity chromatography assay and UCP immunity chromatography assay showed the better specificity and sensitivity.
但现有的纳米金免疫层析技术只能用于定性和半定量的检测，难以满足临床检测指标定量化的要求。
Then, the current GICA can only be applied to qualitative and semiquantitative detection, it cannot satisfy the demand of clinical quantitative detection.
目的根据胶体金免疫层析的原理，建立一种可以在现场快速检测可卡因及其代谢物苯甲酰爱康宁的方法。
Objective To establish a liquid chromatography-tandem mass spectrometry(LC-MS/MS) method for the simultaneous analysis of cocaine(COC) and its metabolite benzoylecgonine(BZE) in urine samples.
基于免疫竞争胶体金免疫层析原理，研制了检测食用肉中呋喃妥因代谢物1-氨基乙内酰脲（AHD）的免疫试纸条。
A method of colloidal gold immunochromatographic assay for the determination of 1-aminohydantoin(AHD) in pork was established based on competition principle.
针对金免疫层析定量测试的要求，将模糊逻辑与人工神经网络相结合，采用模糊神经网络隐式PID控制作为控温方法。
According to the requirement of the GICA strip quantitative detection system, the fuzzy neural networks PID is used by combining fuzzy logic and artificial neural network.
本文研究了金免疫层析试条的智能定量测试系统，着重探讨了中值滤波、小波变换滤波在构建全新的智能金免疫层析试条测试系统中的应用。
The thesis studies the smart quantitative measurement system of immune colloidal-gold strips, specially on the application of median filtering and wavelet in the system.
多克隆抗体由合成化肽段免疫动物，该合成肽段与YAP人源蛋白序列一致，抗体由蛋白a和肽段亲和层析技术纯化。
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the human sequence of YAP. Antibodies are purified by protein a and peptide affinity chromatography.
该多克隆抗体由合成的人类CDK5氨基酸序列对应肽段免疫动物而制成。该抗体使用蛋白A和多肽亲和层析纯化而得。
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence of human CDK5. Antibodies are purified by protein A and peptide affinity chromatography.
该多克隆抗体用与人类PKM2蛋白氨基酸序列对应的人工合成肽段免疫动物制成。该抗体使用蛋白A和肽亲和层析纯化而得。
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence of human PKM2. Antibodies are purified by protein A and peptide affinity chromatography.
多克隆抗体是通过一种合成的肽段去免疫动物产生。这种合成的肽段与包围于人源APC蛋白序列一致，抗体由蛋白a和肽段亲和层析技术纯化。
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence of human APC. Antibodies are purified by protein a and peptide affinity chromatography.
该多克隆抗体是采用合成的与人源mek1蛋白相一致的肽段免疫动物后产生的。该抗体经蛋白a和肽亲和层析纯化。
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to human MEK1. Antibodies are purified by protein a and peptide affinity chromatography.
该多克隆抗体是由合成的人源的针对PRAS40 蛋白氨基酸序列的肽段免疫动物而生产的。抗体由肽亲和层析技术纯化。
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence of human PRAS40. Antibodies are purified by peptide affinity chromatography.
该多克隆抗体用与人类LDHA氨基酸序列对应的人工合成肽段免疫动物制成。该抗体使用蛋白亲和层析纯化而得。
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence of human LDHA. Antibodies are purified by peptide affinity chromatography.
该抗体通过使用合成肽段免疫动物而获得，并经蛋白a和肽亲和层析纯化。
Antibodies are produced by immunizing animals with synthetic peptides, and are purified by combinations of Protein a and peptide affinity chromatography.
该抗体通过使用合成肽段免疫动物而获得，并经蛋白a和肽亲和层析纯化。
Antibodies are produced by immunizing animals with synthetic peptides, and are purified by combinations of Protein a and peptide affinity chromatography.
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