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用于啮齿动物神经发生的BrdU检测法。

BrdU assay for neurogenesis in rodents.

作者信息

Wojtowicz J Martin, Kee Nohjin

机构信息

Department of Physiology, University of Toronto, Toronto, Ontario, Canada M5S 1A8.

出版信息

Nat Protoc. 2006;1(3):1399-405. doi: 10.1038/nprot.2006.224.

Abstract

Neurogenesis within the adult central nervous system is demonstrated using an exogenous cell tracer, 5'-bromo-2'-deoxyuridine (BrdU), in combination with endogenous neuronal markers. Specific primary antibodies raised against these markers are widely available and their visualization is possible with the use of fluorescently tagged secondary antibodies. BrdU is a thymidine analog that incorporates into dividing cells during DNA synthesis. Once incorporated into the new DNA, BrdU will remain in place and be passed down to daughter cells following division. Typically, BrdU is injected intraperitoneally. Different survival times required by the desired experimental time-line will yield data on specific phases of neurogenesis: proliferation, differentiation and maturation. One of the drawbacks of using BrdU is the dependence on a stressful injection procedure and uncertain penetration of the targeted cells with a uniform concentration of the compound. Thus, for experiments requiring measurements of cell proliferation, Ki67 can be used as an acceptable alternative. The protocol takes 3-5 d, allowing for sectioning and staining.

摘要

使用外源性细胞追踪剂5'-溴-2'-脱氧尿苷(BrdU)并结合内源性神经元标记物,可证明成体中枢神经系统内的神经发生。针对这些标记物产生的特异性一抗广泛可得,并且使用荧光标记的二抗可以实现它们的可视化。BrdU是一种胸腺嘧啶类似物,在DNA合成过程中掺入正在分裂的细胞中。一旦掺入新的DNA中,BrdU将保留在原位,并在细胞分裂后传递给子细胞。通常,BrdU通过腹腔注射。所需实验时间线所需的不同存活时间将产生关于神经发生特定阶段的数据:增殖、分化和成熟。使用BrdU的缺点之一是依赖于有压力的注射程序以及化合物浓度均匀时对靶细胞的穿透不确定。因此,对于需要测量细胞增殖的实验,Ki67可以用作可接受的替代物。该方案需要3-5天,以便进行切片和染色。

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