Maximal binding volume of glucocorticoid receptor (GR) in hepatic tissue was assayed by radio-ligand binding assay and protein content was assayed by Western blot.
肝组织GR采用放射性配体结合分析法测定其最大结合容量以及用免疫印迹法测定其蛋白含量。
The experiment was performed by using in situ hybridization, NADPH NBT histochemistry, RNA dot blot and protein dot blot techniques.
实验采用原位杂交，NADPH -NBT组织化学，RNA斑点印迹及蛋白质斑点印迹技术。
To elucidate the effect of the semi-dry electrophoretic transfer and its influencing factors in Western blot, the protein marker and purified recombination protein were used to analyzed.
采用蛋白质分子量标准物和纯化的重组蛋白质进行半干式蛋白质印迹，探讨半干式电泳印迹的多种因素对印迹效果的影响。
The content of heat shock protein 72 (HSP72) in cardiac muscle was measured by dot blot analysis.
斑点印迹法测定心肌热休克蛋白72含量。
The fusion protein has been proved having immunogenicity when detected by Western blot, which demonstrates that it may be useful in the development of porcine pleuropneumonia subunit vaccine.
该融合蛋白的成功表达为猪传染性胸膜肺炎亚单位疫苗的研制奠定了基础。
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。
Using Southern blot of gene localization, vegetative insecticidal protein gene was determined neither on chromosome nor circle plasmids.
营养期杀虫蛋白是在苏云金芽胞杆菌营养期中发现的一种非晶体状胞外杀虫蛋白。
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 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。
Method:The protein of p16 was examined by Western blot in 6 cases of normal pituitary and 40 pituitary adenomas.
方法应用蛋白质杂交技术分析P16在垂体腺癌中的表达。
Western blot analysis of the GST-TM fusion protein using sera from subjects with crustacean allergy confirmed that TM is the major allergen of Chinese mitten crab.
通过与甲壳类过敏患者血清的免疫印迹反应，证实融合表达的原肌球蛋白具有过敏原性，表明原肌球蛋白是蟹类的主要过敏原之一。
Results The RSV G glycoprotein was expressed by the recombinant vaccinia virus, which was determined by Western blot with anti-G protein specific monoclonal antibody.
结果RSV地方株G蛋白在痘苗病毒中获得较好的表达，表达产物的糖基化程度较高，且该重组病毒免疫家兔可诱发特异性抗体产生。
Results The RSV G glycoprotein was expressed by the recombinant vaccinia virus, which was determined by Western blot with anti-G protein specific monoclonal antibody.
结果RSV地方株G蛋白在痘苗病毒中获得较好的表达，表达产物的糖基化程度较高，且该重组病毒免疫家兔可诱发特异性抗体产生。
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