The nutritional status and affecting factors of 35 CHD patients were studied by anthropometric measurement and plasma protein assay.
通过人体学测量及几种血浆蛋白的测定，对35例维持性血液透析患者的营养状况及其影响因素进行调查分析。
Simple, direct and automation-ready procedures for measuring protein concentration are very desirable. our QuantiChromTM protein assay kit is based on an improved Coomassie Blue G method.
简单、直接、自动化的蛋白质浓度检测方法是最为理想的。本公司生产的蛋白质测试法是基于改进的考马斯蓝G的方法。
The amount of adsorbed protein on original and modified silicon surfaces was measured by a Coomassie brilliant blue protein assay. Cell adhesion behavior was then assessed by fluorescence microscopy.
用改良的考马斯亮蓝法对硅片和改性后的硅片进行了蛋白质吸附研究，并采用荧光显微镜观察了胎鼠海马神经细胞在改性前后硅表面的黏附行为。
Methods Using Enzyme Immunosorbent Assay detected urine micro protein.
方法用酶联免疫吸附法测定尿微量蛋白。
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。
Kinase Buffer can be used to assay protein kinase activity.
激酶缓冲液用来分析蛋白激酶的活性。
An indirect hemagglutination assay (IHA) was set up using sheep erythrocytes sensitized with capsid protein VP2 of infectious bursal disease virus (IBDV) which were expressed in Escherichia coli.
以大肠杆菌表达的传染性法氏囊病病毒(IBDV)衣壳蛋白vp2致敏绵羊红细胞，建立间接血凝试验(IHA)。
ConclusionThe assay to determine HCP content in recombinant protein pharmaceuticals should be established based on the respective manufacture process of each product.
结论重组蛋白质药物宿主蛋白质含量测定应依据不同的工艺，制定不同的方法。
To study the application of fluorescent protein phosphatase inhibition assay for the Detection of microcystins in water.
探讨荧光蛋白磷酸酶抑制法在水体微囊藻毒素检测中的应用。
The effect of the recombinant protein on proliferation of human umbilical vein endothelial cells (HUVECs) was also analyzed using the MTT assay.
采用噻唑蓝（MTT）比色法测定表达蛋白抑制血管内皮细胞的活性。
Glucose transporter 1 protein detected by enzyme-linked immunosorbent assay and immunocytochemistry: a useful diagnostic tool for malignant pleural effusions.
用酶联免疫吸附试验和免疫细胞化学法检测葡萄糖转运蛋白1：一种诊断恶性胸水的有用工具。
We used gel retardation assay experiment and green fluorescence protein marker to investigate their transfer efficiency.
用电泳实验和绿色荧光蛋白标记方法研究了它的转染效率。
The von Willebrand's disease factors in plasm, adjusted protein of thrombase and inhibitor 1 of activator of plasminogen were detected with enzyme-linked immunosorbent assay.
用酶联免疫吸附法检测血浆血管性假性血友病因子、凝血酶调节蛋白、纤溶酶原激活物抑制物1水平。
The objective of this study was to determine the role of GLUT1 protein in diagnosing malignant pleural effusions by enzyme-linked immunosorbent assay (ELISA) and immunocytochemistry.
本研究的目的是用酶联免疫吸附试验(ELISA)和免疫细胞化学法判定GLUT 1蛋白在诊断恶性胸水中的作用。
Protein kinase assay was used to detect the activity of MKK6 in cells.
使用激酶活性测定法检测细胞内mkk6的激酶活性。
Objective To study the clinical applicability of C-12 varied tumour markers protein chip assay system.
目的研究c - 12多种肿瘤标志物蛋白芯片检测系统的临床适用性。
Objective Identification of clinical applications to cancer diagnosis with multi-tumor markers protein chip and chemiluminescence assay.
目的探讨多肿瘤标志物蛋白芯片与化学发光检测对肿瘤诊断的临床应用价值。
Methods: The co immunoprecipitation assay was employed to isolate TRF1 protein complex and the immunoprecipitate was subjected to MALDI TOF mass spectrometry for protein identification.
方法：以TRF1抗体应用免疫共沉淀方法，从细胞蛋白抽提物中分离TRF1蛋白复合物，并作蛋白质肽指纹谱鉴定；
In HEK293T, Dual-Luciferase Reporter Assay System was used to evaluate the effect of E4B on TLR pathway, and co-immunoprecipitation was used to identify interactive protein.
在HEK293T细胞中，通过双荧光报告系统检测E4B对TLR信号通路的影响，并且用免疫共沉淀的方法鉴定E4B的相互作用蛋白质。
Objective: to establish a high sensitive bio-bar codes assay method for detecting bluetongue virus (BTV) VP7 protein.
目的：建立高灵敏检测蓝舌病毒VP7蛋白的生物条形码检测方法。
The expression of P27 protein was investigated in 40 cases of odontogenic tumors by immunohistochemical SP assay.
采用免疫组织化学s - P法检测40例牙源性肿瘤中P 27蛋白表达情况。
An indirect enzyme-linked immunosorbent assay (ELISA) was developed based on a purified recombinant F41 pili protein of enterotoxigenic Escherichia coli (ETEC).
以纯化的重组F41菌毛蛋白作为检测抗原，建立了检测产肠毒素大肠杆菌F41菌毛抗体的间接ELISA方法。
A method for the assay of serum protein acetyl cellulose electrophoresis pattern by simple scanning quantitation was described.
实验建立血清蛋白醋纤膜电泳简易扫描定量分析法。
The biotin binding and immunocytochemistry assay indicated that the expressed fusion protein was capable of binding biotin molecule and CEA antigen respectively.
活性鉴定表明该融合蛋白具有结合CEA及生物素的双特异性。
Besides, the result of agglutination activity assay indicated the fusion protein still presented agglutination activity.
经凝血活性测定表明该融合蛋白具有凝血活性。
This paper reports the application of fluorescence anisotropy technique to the (assay) of proteases via a protein substrate labeled with tetramethyl isothiocyanate rhodmine(TMRITC).
建立了一种基于荧光各向异性原理均相测定蛋白酶及其抑制剂的方法。
Methods Serum S100 protein levels were detected by enzyme-linked immunosorbent assay in 86 astrocytoma patients in the course of radiotherapy.
方法采用酶联免疫吸附试验检测86例星形细胞瘤术后患者放射治疗前后血清S100蛋白水平。
Antitumor effect of the Mistletoe protein extract was studied by analysis of cytotoxicity activity of tumor cells in vitro using MTT assay. The validity of this test method was also detected.
采用MTT比色法对体外培养的肿瘤细胞进行细胞毒作用实验，验证槲寄生蛋白注射液体外抗肿瘤效果，并且鉴定这种检测方法的有效性。
Conclusions This assay can be as sensitive and rapid a method for protein quantities.
结论双波长法可作为一种快速、灵敏的蛋白质检测方法。
Conclusions This assay can be as sensitive and rapid a method for protein quantities.
结论双波长法可作为一种快速、灵敏的蛋白质检测方法。
应用推荐