Objective To develop a quantitative ELISA for detection of laminin.
目的建立酶联免疫吸附试验，对层粘连蛋白进行定量检测。
Conclusions Antibody-sandwich ELISA for detection of mp antigen is simple, rapid, sensitive and specific.
结论建立的双抗体夹心elisa检测MP抗原具有快速、简便、灵敏度高、特异性强等优点。
To develop a sensitive and specific ELISA for detection of antibodies to the nonstructural protein of FMDV.
旨在建立一种检测口蹄疫病毒非结构蛋白抗体的敏感、特异的ELISA方法。
Objective To evaluate the value of PCR-probe hybridization-ELISA for detection of mycobacterium tuberculosis(M. tuberculosis).
目的评价聚合酶链反应探针杂交酶显色方法，检测结核分支杆菌。
The results showed that the sensitivity of ELISA for detection of anti-ascaris antibodies was high and there was some cross reaction with other intestinal nematodes.
结果表明，此法诊断蛔虫感染具有较高的敏感性，但与肠道其它线虫感染血清有一定交叉反应。
Nasopharyngeal swabs taken from 328 neonates with pneumonia were analyzed by LCR-ELISA and cell culture. Results A method of LCR-ELISA for detection C. trachomatis infection was established.
采集328份肺炎新生儿鼻咽标本，分别对其进行培养和LCR扩增，应用ELISA检测有无沙眼衣原体感染。
Design experiments and optimize assay performance for biomarker compounds using ELISA, SPR, and fluorescence detection.
设计实验和用elisa、SPR和荧光检测等方法优化生物标记化合物的检测。
Objective To prepare monoclonal antibodies(McAbs) of Mycoplasma hyorhinis and establish an antibody-sandwich ELISA method for the detection of the organism.
目的制备多种抗猪鼻支原体的单克隆抗体，建立双抗体夹心ELISA方法用于该病原体的检测。
The methodology of indirect ELISA for the detection of rotavirus (RV) serum antibody has been investigated.
本文对ELISA间接法检测人轮状病毒（RV）血清抗体的方法学进行了探讨。
Objective To establish the ELISA method for detection of anti-Trichinella antibodies in muscle juice of infected mice.
目的建立检测小鼠肉汁中旋毛虫抗体的酶联免疫吸附试验(ELISA)方法。
Using recombinant nucleocapsid protein GST-N of porcine reproductive and respiratory syndrome virus (PRRSV) as antigen, an indirect ELISA for the detection of antibodies against PRRSV was developed.
用亲和层析纯化的猪繁殖与呼吸综合征病毒(PRRSV)重组核衣壳蛋白gst - N作为诊断抗原，建立检测prrs血清抗体的间接ELISA方法。
The indirect ELISA is widely used for detection of antibodies and coating antigen is very important to the accuracy of ELISA experiment.
本试验分别使用超声波裂解抗原、脂多糖蛋白抗原和全菌抗原作为包被抗原，建立相应的检测方法并进行重复性试验。
Objective to develop a indirect ELISA method for the detection of plasma anti-CA iv antibody and to evaluate the relationship between anti-CA iv antibody with pathogenesis of ns, CGN and 2-dn.
目的建立使用间接酶联免疫吸附法(ELISA)检测人血浆抗碳酸酐酶iv抗体的方法，阐明血浆抗碳酸酐酶iv抗体滴度与肾病综征合(ns)、慢性肾小球肾炎(CGN)和2 -型糖尿病肾病(2 - DN)三种肾脏病的联系。
A double antibody sandwich ELISA for RV antigen was developed using McAb 4c2 as capture antibody and rabbit PcAb as detection antibody.
以单克隆抗体4c2作为捕捉抗体，兔多克隆抗体作为检测抗体，建立了ELISA双抗体夹心法，检测RV抗原。
This article describes the ELISA for the detection of circulating immune complexes based on their recognition by bovine conglutinin.
本文介绍了一种检测循环免疫复合物的牛胶固素酶联免疫吸附试验。
A one step dot ELISA using this specific McAb and a 2nd antibody was used for detection of circulating schistosome antigen in the urine of infected rabbits.
用单抗二抗一步法酶联免疫试验检测感染家兔中的日本血吸虫循环抗原。
The detection rates of TD-PCR for clinical samples were the same as that of ELISA (100%), and higher than that of viral isolation (75%).
运用TD - P CR、ELISA以及病毒分离对临床病料进行检测，TD - PCR方法与ELISA检测结果一致(100%)，均比病毒分离检出率(75%)高。
Thus, indirect ELISA proved to possess high sensitivity, specificity and reproducibility, it can be used to replace indirect sandwich ELISA for the detection of serum antibody against RV.
因此，ELISA间接法敏感性高、特异性强和重复性好，可代替ELISA间接双抗体夹心法以检测RV血清抗体。
By using avian influenza polyclonal antibody and H9 subtype-specific monoclonal antibody, a H9 subtype specific antigen capture ELISA was developed for detection of H9 subtype avian influenza virus.
采用禽流感病毒多克隆抗体及H9亚型特异性单克隆抗体，研究建立H9亚型特异性抗原捕捉elisa检测方法，用于检测H9亚型禽流感病毒。
The virus RNA without purification could be detected with ELISA technique, which is simpler and rapider than RT-PCR technique, and is more suitable for the detection of a great number samples.
ELISA可在不需提纯病毒RNA的情况下实现对病毒的检测，较RT - P CR检测技术快速、简捷，更适合于大量样品的检测。
Objective An ELISA method for the detection of antibody to mouse Mycoplasma pulmonis (M. pul) was established.
目的建立小鼠肺支原体抗体ELISA检测法。
Conclusion The method of PCR-ELISA we established for early detection and typing of all 4dengue viruses seretypes.
结论所建立的方法可用作登革病毒感染的早期诊断及分型。
Conclusion The method of PCR-ELISA we established for early detection and typing of all 4dengue viruses seretypes.
结论所建立的方法可用作登革病毒感染的早期诊断及分型。
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