The eluted sample can then be analyzed by western blot.
稀释的样品可以随后用于western blot分析。
Western blot showed the good immunological specificity of the IgY.
经免疫印迹分析，具有良好的免疫学特异性。
Western Blot assay shows the purified antibody have higher specificity.
实验表明纯化后的抗体具有较高特异性。
Western blot analysis of extracts of various cell lines using TACE Antibody.
使用TACE抗体对多种细胞提取物进行western blot分析。
Western blot analysis of extracts from various cell lines using GIT2 Antibody.
使用GIT2抗体对多种细胞提取物进行western blot分析。
Western blot analysis of extracts from various cell lines, using FAK Antibody.
使用FAK抗体对多种细胞提取物进行western blot分析。
Western blot analysis of extracts from various cell lines using BMPR2 Antibody.
使用BMPR2抗体与多种细胞提取物进行western blot实验。
Western blot analysis of extracts from various cell lines, using Paxillin Antibody.
使用Paxillin抗体对多种细胞提取物进行western blot分析。
Western blot analysis of extracts from various cell lines using TAZ (V386) Antibody.
使用TAZ (V386)抗体对多种细胞提取物进行Western blot分析。
Methods To analyze the clinical data of 15 AIDS patients identified by western blot test.
方法分析经免疫印迹检测证实的15例aids病人的临床资料。
The content of heat shock protein 70 in myocardium was detected with western blot method.
采用蛋白印迹法测定心肌细胞中热休克蛋白70含量。
Western blot analysis of extracts from various cell lines using Numb (C29G11) Rabbit mAb.
使用Numb (C29G11)兔单抗对多种细胞提取物进行western blot分析。
Western blot analysis of extracts from various cell and tissue types using Vinculin Antibody.
使用Vinculin抗体对多种细胞和组织提取物进行western blot分析。
Western blot analysis revealed that the antiserum against DNA2 encoding protein was obtained.
这个结果证明我们已成功获得DNA2编码蛋白的血清。
The expression of the above three HA DNA vaccines was verified in 293t cells by Western blot analysis.
用这3种重组质粒分别转染293t细胞，蛋白表达经蛋白质印迹检测得到确认。
Its immunoreactivity was analyzed by Western blot, ELISA and blocking ELISA using MAb and positive serum.
采用单克隆抗体和阳性血清经elisa、阻断elisa、免疫印迹分析重组蛋白的免疫反应性。
Methods MMP-9 and TIMP proteins were examined by using zymographic analysis and Western blot in 41 cases with ESCC.
方法免疫组化法分别检测41例食管鳞癌患者的癌及相应正常组织中MMP-9和TIMP的表达变化。
UAF were analyzed with Western Blot, integrated density value were determined and relative excretion rate was counted.
采用免疫印迹法测定uaf，并测定其积分密度值，计算相对排泄率。
Western blot analysis of partially purified, concentrated, serum-free medium containing human MMP-9, using MMP-9 Antibody.
含有人MMP - 9的无血清培养基经过部分纯化，浓缩后使用MMP - 9抗体进行western blot分析。
The expression level of NGAL in 5 esophageal carcinoma cell lines was also examined by immunofluorescence and western blot.
运用免疫荧光和蛋白印迹技术检测了5种食管癌细胞系中NGAL的表达。
Methods HIV antibody were screened by ELISA and confirmed by western blot( WB)in 2 272 patients diagnosed with tuberculosis.
方法对2 272例诊断为结核病的住院病人进行HIV抗体检测，初筛阳性者进一步做免疫印迹试验（WB）。
The misuse and re-use of western blot bands violated the editorial policy of Journal of Cell Science, and so we must retract this article.
作者表示，该论文滥用和重复使用他们发表的其他论文中的蛋白 免疫印迹图片，违背了《细胞科学期刊》的编辑政策，必须撤销。
Western blot analysis of extracts from COS cells, untransfected or transfected with mouse endoglin, using Endoglin Antibody (Mouse Specific).
使用Endoglin抗体（鼠特异性）对未转染或转染了小鼠endoglin的COS细胞提取物进行western blot分析。
The aliquot of proteins was subjected to SDS-PAGE, followed by Western blot analysis in which individual sera were tested for primary antibody.
用肺癌患者及健康对照者的血清作第一抗体进行蛋白印迹检测。
Western blot analysis revealed that the human UREB1 was present in all tumor tissues but the quantity of UREB1 in different tissues was not the same.
在各种肿瘤组织中都有UREB1的表达，但是表达水平及定位不一样。
The expressions of both FGFR1 and FGFR2 increased gradually with kidney development shown by computerized densitometry, stereography and Western blot.
图像分析结果显示，随着肾脏的发育，FGFR1、FGFR2表达逐渐增高。
They then checked 229 positive patients with the gold-standard laboratory test, a Western blot. More than 10% of the rapid tests were giving false bad news.
之后，他们又应用金标准试验——蛋白印迹法(Western blot)检测了229名阳性患者，结果表明快速检测结果中有超过10%为假阳性。
Objective To develope a western blot of human plasma factor V (FV) and conduct immunoblot analyses on riasma FV from a family with hereditary FV deficiency.
目的建立人血浆因子V（FV）蛋白免疫印迹分析，对遗传性FV缺乏症家系成员血浆FV含量进行分析。
The results showed recombinant NP protein could bind to both positive serum and MAb with specificity in ELISA, but only bind to positive serum in western blot.
结果表明：所获得的重组NP蛋白在ELISA分析中均能与阳性血清和单克隆抗体发生特异性结合，但在免疫印迹分析中仅与阳性血清发生特异性结合。
The results showed recombinant NP protein could bind to both positive serum and MAb with specificity in ELISA, but only bind to positive serum in western blot.
结果表明：所获得的重组NP蛋白在ELISA分析中均能与阳性血清和单克隆抗体发生特异性结合，但在免疫印迹分析中仅与阳性血清发生特异性结合。
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