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    • 1. 发明申请
    • Mechanical Zoom Imaging Apparatus
    • 机械变焦成像设备
    • US20150029595A1
    • 2015-01-29
    • US14444709
    • 2014-07-28
    • Bio-Rad Laboratories, Inc.
    • Steve SwihartEvan ThrushEvelio PerezKevin McDonald
    • G02B15/14
    • G02B15/14
    • An imaging assembly for the viewing, imaging, and analysis of chemiluminescent or bioluminescent samples in gels or other substrates, in which an adjustable camera and lens module having a prime or fixed lens or a focusing lens is moved to change the field of view by shifting the focal plane of the camera and lens module. The imaging assembly can also include a mirror to bend or fold the optical path between the camera and lens module and the target area having a sample, in which the mirror can move in the same vertical direction as the camera and lens module. Further, the camera and lens module can be configured to more move in a diagonal direction relative to the location of the imaging target area. The imaging assembly can further have a duct system adaptable to adjust with the movement of the camera and lens module.
    • 用于在凝胶或其它基底中观察,成像和分析化学发光或生物发光样品的成像组件,其中具有主要或固定透镜或聚焦透镜的可调节照相机和透镜模块移动以通过移动来改变视场 相机和镜头模块的焦平面。 成像组件还可以包括用于弯曲或折叠相机和透镜模块之间的光路的反射镜和具有样品的目标区域,其中反射镜可以在与相机和透镜模块相同的垂直方向上移动。 此外,相机和透镜模块可以被配置为相对于成像目标区域的位置在对角线方向上更多地移动。 成像组件还可以具有适于根据相机和透镜模块的运动进行调节的管道系统。
    • 7. 发明申请
    • STAIN-FREE PROTEIN QUANTIFICATION AND NORMALIZATION
    • 无蛋白质定量和正常化
    • US20130288388A1
    • 2013-10-31
    • US13870710
    • 2013-04-25
    • BIO-RAD LABORATORIES, INC., LSG - LSD DIVISION
    • Steve FreebyNing LiuKevin McDonaldAran PaulusAnton Posch
    • G01N33/53
    • G01N33/53G01N33/6827G06F19/10G06T7/0012G06T11/60G06T2207/30004
    • Disclosed herein are methods of protein quantification and normalization using haloalkylated tryptophan fluorescence. Complex protein samples, i.e., samples that each contain 1,000 or more distinct proteins, from diverse sources that do not have common protein profiles are treated with a halo-substituted organic compound (i.e. haloalkane) that reacts with tryptophan residues to form fluorescent products. Irradiation of the samples with ultraviolet light and the detection and quantification of the resultant fluorescent emissions from all proteins in each sample are then used to obtain comparative values for total protein content among the various samples. The values thus obtained are found to be valid indications of comparative total protein content, despite the fact that the tryptophan levels vary widely among the various proteins in any single sample and the samples, due to the diversity of their origins, tend to differ among themselves in the identities and relative amounts of the proteins that they contain. Protein samples are also normalized to correct for differences in sample dilution, sample loading, and protein transfer inconsistencies, by using stain-free detection of total protein in each of the samples, or detection of subsamples within each sample.
    • 本文公开了使用卤代烷基化色氨酸荧光进行蛋白质定量和归一化的方法。 使用与色氨酸残基反应以形成荧光产物的卤素取代的有机化合物(即卤代烷)处理复合蛋白质样品,即每种含有来自不同来源的不具有共同蛋白质谱的1,000个或更多个不同蛋白质的样品。 然后使用紫外光照射样品,并对每个样品中所有蛋白质产生的荧光发射进行检测和定量,以获得各种样品中总蛋白质含量的比较值。 这样获得的值被发现是比较总蛋白质含量的有效指示,尽管事实上,任何单个样品中的各种蛋白质之间的色氨酸水平变化很大,并且样品由于其起源的多样性而趋于彼此不同 在它们所含的蛋白质的身份和相对量中。 蛋白质样品也通过使用每个样品中的总蛋白的无染色检测或每个样品中的子样品检测来校准样品稀释度,样品加载和蛋白质转移不一致性的差异。