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1.Methods Manner plate assay, contact hemolysis and supernatant assay were used.
方法平板检测法,接触溶血法,上清检测法。收藏指正
2.DETERMINATION OF THE ANTIMICROBIAL ACTIVITY OF PROBIOTIC BY OXFORD PLATE ASSAY SYSTEM
用牛津杯法测定益生菌的抑菌活力收藏指正
3.An organic solvent tolerant isolate A213 originating from soil samples were successfully isolated via direct plating method using 10g/L of toluene as the sole carbon source and transparent cycle plate assay method.
通过添加10g/L的甲苯作为唯一碳源进行预培养,然后以透明圈平板筛选法从土壤样品中成功地筛选到了一株耐有机溶剂的产脂肪酶的酵母菌A213,初步鉴定为耶罗威亚酵母(Yarrowia sp.)。收藏指正
4.Using Oxford Plate Assay method, the antibiotic effect measured by the diameter of antibiotic circle of mutational strains includingUV—19、 Co—38、 DES—21 were respectively 1.875、 1.68、 1.52 times than the original strain.
通过硫酸二乙酯诱变得到高产菌株DES—21、DES—31、DES—37,其中菌株DES—21的发酵上清液是原种的1.52倍。收藏指正
5.Conclusion Micro-plate Hybrid Capture Detection PCR Assys is a rapid,easy,sensitive and special assay to detect high-risk HPV infection with cervical cytological specimens,it can be applied for large-scale screening and clinical diagnosis.
结论:PCR微板杂交捕获检测宫颈脱落细胞内高危型HPV感染,具有快速、简便、灵敏度高、特异性强等优点,适用于大规模筛查和临床常规工作。收藏指正
6.Using a self prepared coated ELISA plate and anti dsDNA quantitative kit of Binding site company of Birmingham medical college U K,and dot immunogold filtration assay have detedted sera of 32 patients with active SLE,6 rheumatoid arthritis and 30 normal controls,results showed,positive consistent rate is respectively 96 9% and 93 8% and negative consistent rate is 96 7%,5 patients with SLE were tested with the detection of quantitative,results were almost consistent.
分别以自制ELISA和Bindingsite公司ELISA抗dsDNA定量剂盒和胶体金斑点免疫渗滤法定性检测了 32例活动期SLE ,6例类风湿关节炎 (RA) ,30例健康人血清 ,阳性符合率分别为 96 9%和 93 8% ,阴性符合率均为 96 7%。收藏指正
7.A Sandwich Enzyme-linked immunosobent assay test Differentiability kit based on previous work was developed for detection of avian influenza virus (AIV) antigen including all AIV subtypes detecting, subtype of ATV H5 and subtype of AIV H9. The kit consists of twelve reagents and a piece of 96 well microtiter plate.
用抗AIV H5亚型血凝素单克隆抗体为包被抗体,兔抗AIV IgG为第二抗体;收藏指正
8.The capsular polysaccharide ( Cps ) of App was extracted and used as antigen for developing a Cps-based indirect enzyme-linked immunosorbent assay ( Cps-ELISA ) . The conditions of Cps-ELISA were determined as follows: 3μg/ml of CPS used to coat ELISA plate, 1:100 of sera as detecting samples and serum sample being incubatedat 37℃ for 90 minutes.
以三氯乙酸-丙酮法提取的App的荚膜多糖粗提物(capsular polysaccharide,Cps)为抗原建立间接ELISA(Cps-ELISA),经验确定抗原包被浓度为3μg/ml,血清检测稀释度为1:100,抗原与抗体的最佳反应时间为90分钟。收藏指正
9.By using yeast two hybrid system, interaction assay in vitro between ubiquitin and IAP2 or IAP3 of SeMNPV has been done. The putative positive clones only existed in the plate of the SD/-Leu/-Trp/X-α-GAL, which suggested that ubiquitin might interact with IAP2 or IAP3 weakly, since ubiquitin may be transferred to IAP2 or IAP3 through E1 and E2 in yeast.
实验表明,用Clontech 公司的MACHMAKER GAL4 Two-hybrid system 3,只在低严谨型筛选培养基上得到了一些阳性克隆,这说明Ubiqutin和IAP2, IAP3在体外可能存在着较弱的相互作用,这种相互作用也可能是因为Ubiqutin和IAP利用了酵母中本身存在的E1和E2。收藏指正
10.Methods The cultured human umbilical vein endothelial cells (HUVEC) and bovine vascular smooth muscle cells (VSMC)were treated with 0, 1.25, 2.5, 5.0, 10, 20, 40 Gy32P beta irradiation, respectively. The proliferation of the cells was then measured using colorimetric assay and analyzed with an ELBA plate reader. The erasion trace test was performed to discern the cellular inhibition of HUVEC and VSMC proliferation.
方法 培养人脐静脉内皮细胞和牛主动脉平滑肌细胞,接受0、1.25、2.5、5.0、10、20、40 Gy β射线后,以四唑盐(MTT)比色实验评价剂量-效应关系,用划痕实验研究β射线对两种细胞增殖的影响。收藏指正
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