Effect of hyperbilirubinemia on determination of serum HDL-c using enzyme assay 高胆红素影响酶法测定血清高密度脂蛋白-胆固醇
Experimental study on enzyme dot assay for detection of hemorrhagic fever with renal syndrome antigen 免疫酶斑点法检测汉坦病毒抗原的研究
The gene structure, biochemical characteristics, biological functions in solubilizing fibrin, enzyme activity assay, isolation and purification of nattokinase are reviewed in this paper. 本文就纳豆激酶的基因结构、生化特性、生物学功能、酶活性测定及分离纯化等方面进行了综述。
Antibody Detection in Brucellosis Patients by Immune Enzyme Dot Assay with Outer Membrane Protein Antigen 用布鲁氏菌膜蛋白抗原的免疫酶斑点试验检测布鲁氏菌病患者抗体
The enzyme assay is comparatively steady, suitable to a large quantity of samples, but it is not preferable when the sample is deep jaundice, chyle blood, or hemolysis. 酶法较为稳定,适合全自动化仪器和大批量标本检测的应用,但对黄疸较深和乳糜血、溶血等标本结果影响较大。
The NO was detected by enzyme assay. 酶法测定NO活性。
In view of these, the authors give here a comprehensive commentary on some common techniques in mutant isolation, enzyme assay and signal detection and their progress recently. 居于此,文中综合评述在突变株分离、酶检测和信号探测等方面,目前的一些常用技术及其最新进展。
Comparison between the enzyme assay and ion selective electrode assay to measure serum calcium 酶法、离子选择电极法检测血清钙方法的比较
Research on mechanism of anti-ageing of brain of mice and rats by traditional Chinese medicine of tonifying the kidney and tonifying the deficient essence with radiochemical method of enzyme assay 用放射酶分析法研究补肾填精中药延缓鼠脑组织衰老的机理
The heme oxygenase-1 ( HO-1) activity was analyzed by the enzyme assay. 以酶化学法观察其对脾细胞血红素氧合酶1(HemeOxygenase1,HO1)活性的影响。
The content of the total cholesterol, triglyceride and the high density lipoprotein cholesterol in the blood plasma were measured by enzyme assay. 并用酶法分别测定血浆总胆固醇、甘油三酯和高密度脂蛋白胆固醇含量。
Restriction enzyme assay, PCR and sequencing confirmed that the TK gene was obtained successfully. Only one Kpn ⅰ site and a transcription termination signal TTTTT N ( T) T were found in the gene. 酶切鉴定、PCR鉴定和测序结果表明,成功获得了TK基因,获得的TK基因内存在一个KpnⅠ酶切位点和编码区的早期转录终止信号TTTTTN(T)T。
Results Enzyme assay showed that purified MutS had the activity for recognizing and binding mismatch duplex DNA. 结果纯化后的MutS具有识别、结合错配DNA双链的活性。
The infarct size was measured by NBT staining. The expression of intercellular adhesion molecule-1 ( ICAM-1) was monitored by immunoassay. The adhesion rate of leukocytes and infiltration of leukocytes in 12 hours after operation were determined by marrow peroxide enzyme assay. kg-1剂量组,用NBT染色法检测心肌梗死范围,免疫组织化学法检测心肌细胞间黏附分子(ICAM-1)表达,髓过氧化物酶法检测心肌白细胞黏附率。
This paper includes the following contends: In chapter one, the assay methods of activity of enzyme, and the factors of enzyme catalyzed reaction and the application of fluorophotometry in enzyme assay were summarized. 第一章综述了酶活力的测定方法,影响酶催化反应的因素,荧光分析方法在酶分析中的应用。
Factors influencing enzymatic reaction were analysed for enzyme assay and industrial application in the future. 为了确定酶活测定条件并为今后的酶反应工艺条件提供一定的参考,对影响酶反应的几种因素进行实验。
The characteristic of intermediates were analyzed by refractive index and UV IV spectrum. The structure of final product was confirmed by UV VIS,~ 1H NMR,~ ( 13) C NMR and application to enzyme assay. 对中间体的折光率和紫外-可见光谱进行分析,并通过紫外-可见光谱1、H-NMR和13C-NMR以及酶分析应用对最终产物进行确证。
Methods: Effects of three immobilized materials, temperature, pH, monovalent canons and alcohol on the activity of tryptophanase of immobilized WW-11 were observed by enzyme assay. 方法;通过色氨酸酶活力测定,考察三种固定化材料及温度、pH、单价阳离子和乙醇对固定化WW-11色氨酸酶活力的影响。
The bacteria resource of enzyme is significant to pyruvate production by enzymatic method, and to the enzyme assay of lactate for medical diagnosis, and the application of enzyme electronic probe. 这一酶源在酶法生产丙酮酸及医疗诊断和酶电极应用上有意义。
Results Restriction enzyme assay and DNA sequencing showed the β 2 m gene was cloned and the vector was constructed successfully. 结果酶切和测序证实β2m基因克隆和载体构建成功,目的蛋白在宿主菌中高效表达于包涵体中;
This thesis consists of two parts: I. Microreactor fabrication and enzyme assay combining microreactor with Scanning Electrochemical Microscopy ( SECM). 本论文共分两部分:Ⅰ.微反应器的构建、表征及结合扫描电化学显微术(ScanningElectrochemicalMicroscopy,SECM)的应用;
In order to establish a molecular model based on RmlC enzyme assay to screen inhibitors of RmlC, a large amount of RmlC protein must be acquired. 为了建立体外筛选RmlC酶抑制剂的分子模型,我们需要获得高纯度的RmlC酶蛋白,并为建立快速、精确的酶活性测定方法和研究酶促反应动力学特性提供物质保障。
The activity of γ-GCS was measured by coupled enzyme assay. 双酶法测γ-GCS的活性。
Methods 88 patients with hyperthyroidism and 46 healthy volunteers were assayed respectively. The plasma levels of ET and NO were measured by RIA and enzyme assay. Thyroxin were measured by chemiluminescent immunoassay. 方法用放射免疫法,酶法和化学发光法分别测定了88例甲亢患者的血浆内皮素、一氧化氮和甲状腺素,同时测定对照组46例健康者,将两组结果进行比较。
These thermo kinetic parameters are good indicators to observe the changes of microbial activity and they are in good agreement with the OD of microbe and enzyme assay data. 这些热动力学参数是反应生物活性变化的较好指标,并与生物量和酶分析数据相一致。
Most of the β-glucosidase activity was located on the cell surface of C. hutchinsonii from the enzyme assay, although the genomic analysis showed that all the candidate β-glucosidases were predicted to be located in the periplasmic space. 虽然基因组序列分析预测可能的β-葡萄糖苷酶都位于细胞周质,但是多次酶活实验表明大部分的β-葡萄糖苷酶活力位于细胞表面。