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Embedding moulds:Peel-A-Way® embedding moulds

Company: Sigma-Aldrich
Catalog#: E6032-1CS
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Single or Repeated Ablation of Mouse Olfactory Epithelium by Methimazole
Author:
Date:
2021-04-20
[Abstract]  

Odor-detecting olfactory sensory neurons residing in the nasal olfactory epithelium (OE) are the only neurons in direct contact with the external environment. As a result, these neurons are subjected to chemical, physical, and infectious insults, which may be the underlying reason why neurogenesis occurs in the OE of adult mammals. This feature makes the OE a useful model for studying neurogenesis and neuronal differentiation, with the possibility for systemic as well as local administration of various compounds and infectious agents that may interfere with these cellular processes. Several different chemical compounds have been shown to cause toxic injury to the OE, which can be used for OE ablation. We, and others, have found that the systemic administration of the hyperthyroid drug,

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[摘要]  
[摘要]气味-检测驻留在鼻腔嗅上皮(OE)嗅觉感觉神经元是在与外部环境直接接触仅神经元。其结果是,这些神经元进行化学,物理和传染性损伤,这可能是根本原因的神经发生中发生的的OE成年哺乳动物。这一特点使得该OE一个有用的模型用于研究ING神经和神经元分化,与该 可能会干扰这些细胞过程的各种化合物和感染剂的全身和局部给药的可能性。已示出几个不同的化学化合物以使毒性损伤的OE ,其可用于OE消融。我们和其他人,有无˚F OU次是在甲亢药物的全身给药,他巴唑,可靠地使olfactotoxicity的副作用。 在这里,我们概述了甲咪唑一次或多次消融的OE损伤方案。单甲巯咪唑给药可用作到螺柱ÿ神经上皮再生和干细胞活化,而[R epeated消融和OE的再生使所述螺柱ÿ组织干细胞的耗竭组织化生和产生。


[背景]新的神经元在整个生命中生成的OE的哺乳动物包括呼玛纳秒(哈恩等人,2005)一第二小鼠(Graziadei等人,1979年b;近藤等人,2010) 。Ç ontinuous细胞产生主要由球状祖细胞实现(张等人,2014) 。祖细胞也有重建损伤后所有OE细胞类型的潜力,与水平基底细胞小号公顷咏最大的组织干细胞的潜力(梁等人,2007;施尼特凯等人,2015年; Gadye 。等人,2017年)。

有存在不同的方法来具体伤害的OE在实验室啮齿动物,这又允许再生过程,包括干细胞的活化,神经发生,和神经元分化的研究。方法包括摘除嗅球(OB)(Schwob等,1992),嗅神经轴突切开术(Graziadei等,1979a; ...

Optimized Immunostaining of Embryonic and Early Postnatal Mouse Brain Sections
Author:
Date:
2021-01-05
[Abstract]  

The mammalian neocortex, the outer layer of the cerebrum and most recently evolved brain region, is characterized by its unique areal and laminar organization. Distinct cortical layers and areas can be identified by the protein expression of graded transcription factors and molecular determinants that define the identity of different projection neurons. Thus, specific detection and visualization of protein expression is crucial for assessing the identity of neocortical neurons and, more broadly, for understanding early and late developmental mechanisms and function of this complex system. Several immunostaining/immunofluorescence methods exist to detect protein expression. Published protocols vary with regard to subtle details, which may impact the final outcome of the immunofluorescence.

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[摘要]  [摘要]哺乳动物的新皮层是大脑的外层,也是最近进化的大脑区域,其特征在于其独特的区域和层状组织。不同的皮质层和区域可以通过分级转录因子的蛋白质表达和定义不同投射神经元身份的分子决定簇来鉴定。因此,蛋白质表达的特异性检测和可视化对于评估新皮层神经元的身份至关重要,更广泛地来说,对于理解这个复杂系统的早期和晚期发育机制和功能至关重要。一些 存在免疫染色/免疫荧光方法来检测蛋白质表达。已发布的方案在细节方面有所不同,可能会影响免疫荧光的最终结果。在这里,我们提供了详细的协议,适用于低温恒温器薄切片和厚振动切片器薄切片,该协议已成功地开发了针对新皮质发育关键分子的抗体。从早期的技术措施测距的大脑采集到的图像分析和统计,我们包括有关样品包容和每一个细节部分ING,幻灯片存储和旨在减少非特异性背景最佳抗体稀释。在实验室中常规使用的,我们的背景优化的免疫染色协议允许区域的有效检测-和层-独特新皮层投射神经元的特定的分子决定因素。



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优化的小鼠脑切片免疫染色方案的工作流程图。一。一个流程图的不同步骤的优化免疫染色协议薄低温恒温器和厚振动切片。乙。例如,用于在薄冠状免疫染色对SATB2和CTIP2部(20 μ ...

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