首页> 外国专利> DETECTION AND QUANTIFICATION OF ONE OR MORE TARGET ANALYTES IN A SAMPLE USING SPATIALLY LOCALIZED ANALYTE REPRODUCTION

DETECTION AND QUANTIFICATION OF ONE OR MORE TARGET ANALYTES IN A SAMPLE USING SPATIALLY LOCALIZED ANALYTE REPRODUCTION

机译:使用空间局部化的分析物对样品中一种或多种目标分析物进行检测和定量

摘要

The presence or absence of one or more target microbial analytes in a substance, such as a biological or environmental substance, is assayed by inoculating a growth medium with a sample of the substance. The medium may be combined with a labeled analyte-specific material (LASM) which can migrate through the substrate and which is homogeneously distributed throughout the medium. The LASM may be premixed with the medium, or may be added to the medium after inoculation wi th the substance. The nature of the medium is such that it will support target analyte reproduction so as to form target analyte colonies in or on the medium, and it will not allow the target analyte colonies to migrate on or within the medium. After the sample to be assayed is added to the medium, growth of the target analyte colonies in the sample will bind increasing quantities of the LASM, thereby creating localiz ed intensely labeled areas in the medium which can be visually or photometrical ly detected. As the target analyte colonies grow on or in the medium they attra ct increasing quantities of the LASM which diffuses to the colonies through the medium causing the local target analyte colonies to become intensely labeled, which renders the colonies readily detectable. Each of the intensely labeled target analyt e colonies in the medium may also be surrounded by areas of lower intensity due to loca l depletion of the LASM in the regions of colony growth. The number of intense ly labeled target analyte colonies in the medium will be proportional to the concentration of the target analyte present in the sample. In the event that the target analyte is absent from the sample, then there will be no localized labeled microbe colonies in the medium.
机译:通过在生长培养基中接种该物质的样品,可以测定一种物质(例如生物或环境物质)中是否存在一种或多种目标微生物分析物。介质可以与标记的分析物特异性材料(LASM)结合,后者可以迁移通过基质,并且在整个介质中均匀分布。 LASM可以与培养基预混合,也可以在与物质一起接种后添加到培养基中。介质的性质使得它将支持目标分析物的繁殖,从而在介质中或介质上形成目标分析物菌落,并且将不允许目标分析物菌落在介质上或介质内迁移。在将待分析的样品添加到培养基中后,样品中目标分析物菌落的生长将结合越来越多的LASM,从而在培养基中创建了可以通过视觉或光度法检测到的局部强烈标记区域。随着目标分析物菌落在培养基上或培养基中生长,它们会吸引越来越多的LASM,而LASM会通过培养基扩散到菌落,导致局部目标分析物菌落被强烈标记,从而使菌落易于检测。由于在菌落生长区域中LASM的局部耗竭,培养基中每个标记强烈的目标分析菌落也可能被强度较低的区域包围。培养基中强烈标记的目标分析物菌落的数量将与样品中存在的目标分析物的浓度成正比。如果样品中没有目标分析物,则培养基中将没有定位的标记微生物菌落。

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