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Aqueous two-phase system-mediated antibody micropatterning enables multiplexed immunostaining of cell monolayers and tissues

机译:两相水系统介导的抗体微模式可对细胞单层和组织进行多重免疫染色

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摘要

Conventional immunostaining methods consume large quantities of expensive antibodies and are limited in terms of the number of antigens that can be detected from a single sample. In order to achieve multiplexed immunostaining, we micropatterned antibodies using aqueous two-phase systems (ATPS) formed from polyethylene glycol (PEG) and dextran. Multiple antigens can be detected on a single fixed sample by incorporating antibodies within dextran solutions, which are then patterned by micropipetting at specific sites on the sample in a solution of PEG. The antibodies are retained within the dextran phase due to biomolecular partitioning, allowing multiple protein markers to be visualized simultaneously by way of chromogenic, chemiluminescent, or immunofluorescent detection. This aqueous two-phase system-mediated antibody micropatterning approach allows antibody dilutions to be easily optimized, reduces the consumption of expensive primary antibodies and can prevent antibody cross-reactions, since the antibodies are retained at separate sites within the dextran microdroplets.
机译:常规的免疫染色方法消耗大量昂贵的抗体,并且在可以从单个样品中检测到的抗原数量方面受到限制。为了实现多重免疫染色,我们使用了由聚乙二醇(PEG)和右旋糖酐形成的水性两相系统(ATPS)对抗体进行微模式化。通过在葡聚糖溶液中掺入抗体,可以在单个固定样品上检测多种抗原,然后通过在PEG溶液中样品的特定部位进行微量移液将其图案化。由于生物分子分配,抗体保留在葡聚糖相中,从而允许通过发色,化学发光或免疫荧光检测同时显示多个蛋白质标记。这种含水两相系统介导的抗体微模式化方法可以轻松优化抗体稀释度,减少昂贵的一抗的消耗,并可以防止抗体交叉反应,因为抗体保留在葡聚糖微滴内的不同位置。

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