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首页> 外文期刊>BioTechniques >PBXL-1: A new fluorochrome applied to detection of proteins on membranes
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PBXL-1: A new fluorochrome applied to detection of proteins on membranes

机译:PBXL-1:一种新的荧光染料,用于检测膜上的蛋白质

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摘要

An easy, sensitive and direct fluorescent immunodetection method for proteins is described using the new fluorochrome PBXL(TM)-1 imaged with the FMBIO(R) II Laser Scanning Imaging System. PBXL-1 is derived from a protein supra-molecular complex that contains a large number of chromophores. This complex, the phycobilisome, is extracted from a red alga then chemically stabilized to allow its use in specific binding assays. PBXL-1 was crosslinked to goat anti-rabbit IgG or streptavidin with heterobifunctional cross-linkers. The detection limit of PBXL-1 was determined by applying it on nitrocellulose membranes then imaging the membrane using an ytterbium aluminum garnet (YAG) laser Evaluation of PBXL-1 sensitivity in a specific binding assay was tested on streptavidin/biotin and an antibody system. PBXL-1 provides high sensitivity in direct fluorescent applications due to a physical amplification of signal (i.e., a large number of fluorophores per binding event). PBXL-1 provides a linear response over two orders of magnitude while providing sub-amol sensitivity, indicating broad applicability for detection of a variety of targets. To our knowledge, this is the most sensitive direct fluorescent detection method available.
机译:描述了一种使用FMBIO II激光扫描成像系统成像的新型荧光染料PBXL™-1的简单,灵敏和直接的蛋白质荧光免疫检测方法。 PBXL-1衍生自包含大量生色团的蛋白质超分子复合物。从红藻中提取该复合物,即藻胆体,然后对其进行化学稳定处理,以使其可用于特异性结合测定。 PBXL-1通过异双功能交联剂与山羊抗兔IgG或抗生蛋白链菌素交联。 PBXL-1的检出限是通过将其涂在硝酸纤维素膜上,然后使用an铝石榴石(YAG)激光对膜进行成像来确定的。在链霉亲和素/生物素和抗体系统上测试了特异性结合测定中PBXL-1的敏感性。由于信号的物理放大(即每个结合事件大量的荧光团),PBXL-1在直接荧光应用中提供了高灵敏度。 PBXL-1提供两个数量级的线性响应,同时提供亚摩尔浓度的灵敏度,表明其广泛适用于检测各种目标。据我们所知,这是可用的最灵敏的直接荧光检测方法。

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