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Invitrogen Live/Dead assay kit for mammalian cells, containing green calcein-AM and red ethidium homodimer-1 fluorescent dyes

Company: ThermoFisher
Catalog#: L3224
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Fluidigm Based Single-cell Gene Expression Library Preparation from Patient-derived Small Intestinal Organoids
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Date:
2020-10-05
[Abstract]  In this protocol, we describe our methods to isolate crypts from patients' biopsy samples and to culture human intestinal stem cells as it’s called “organoid.” Beyond that, we describe how to dissociate organoids cells into single cells for single-cell analysis as a further application. This protocol should provide investigators sufficient tools to generate human organoids from biopsy samples and to accomplish a stable in-vitro assay system. [摘要]  [摘要]在此协议中,我们描述了从患者的活检样本中分离隐窝并培养人类肠干细胞(称为“类器官”)的方法。除此之外,我们还介绍了如何将类器官细胞分解为单细胞以进行单细胞分析,作为进一步的应用。该方案应为研究人员提供足够的工具,以从活检样品中产生人类器官并完成稳定的体外测定系统。

[背景]肠上皮是一个多功能组织即编排动态平衡并形成物理屏障。由肠干细胞(ISC)产生的每个肠上皮细胞(IEC)每4-5天更新一次该上皮(Crosnier等,2006 )。ISC位于隐窝的底部,并表达各种文献先前报道的特定标记(Muñoz等,2012 ;Clevers ,2013 )。研究表明,干细胞正确更新的功能障碍与肠道疾病有关,对ISCs动态的了解可能阐明了包括炎症性肠病(IBD)在内的各种疾病的发病机制(Okamoto et al。,2016 )。

然而,由于缺乏能概括生理性肠上皮层的有效模型,因此对肠干细胞特性的研究具有挑战性。史诗般的“类器官”的引入克服了种种障碍(Sato等人,2009和2011 ),可以从单个ISC体外建立类器官,并忠实地保留其起源组织的生理和病理特征(Middendorp等人)。 。,2014 )。类器官已被用于各种胃肠道疾病解剖基础病理变化(Fatehullah 。等人,2016; Noben等人,2017 ...

A Method to Efficiently Cryopreserve Mammalian Cells on Paper Platforms
Author:
Date:
2020-09-20
[Abstract]  This protocol describes a simple method to cryopreserve mammalian cells within filter papers as an alternative to conventional slow-freezing approach. The method involves treating paper fibers with fibronectin, using low concentrations of the cryoprotectant dimethyl sulfoxide (DMSO), and slow freezing cells to -80 °C at a 1 °C min-1 rate. In our method, the biocompatibility, large surface area, 3D porosity and fiber flexibility of the paper, in combination with the fibronectin treatment, yield recovery of cells comparable to conventional approaches, with no additional fine-tuning to freezing and thawing procedures. We expect that the paper-based cryopreservation method will bring several advantages to the field of preserving mammalian cells, including accommodation of a higher ... [摘要]  [摘要] 该协议描述了一种简单的方法,可在滤纸中冷冻保存哺乳动物细胞,以替代常规的慢速冷冻方法。该方法包括使用纤连蛋白处理纸纤维,使用低浓度的冷冻保护剂二甲基亚砜(DMSO),然后以1°C min -1的速率将细胞缓慢冷冻至-80°C 。在我们的方法中,纸的生物相容性,大表面积,3D孔隙率和纤维柔韧性与纤连蛋白处理相结合,可产生与传统方法相当的细胞回收率,而无需对冷冻和解冻程序进行额外的微调。我们期望纸质冷冻保存方法这将为保存哺乳动物细胞领域带来几项优势,包括在单位体积内容纳更多数量的细胞,并且释放后无细胞损失。该方法需要最小的存储空间,在该存储空间中,可以将具有大面积的纸平台卷起和/或折叠并存储在库存中,并允许按需方式有效地运输/分配细胞。此外,该方法的另一个特征包括细胞球体和3D细胞培养物的形成和冷冻保存。


[背景] 哺乳动物细胞的成功保存,长期保存,维护和分配是​​重要的研究领域,目前仍在深入的科学研究中。特别是,冷冻细胞的及时稳定供应与组织工程研究有关,例如细胞培养,药物开发和测试以及再生和生物治疗医学。

当前的常规细胞冷冻保存方案包括缓慢和快速的冷冻和玻璃化(Pegg,2002; Baust 等,2009)。在这些方法中,将各种浓度的冷冻保护剂添加到细胞悬浮液中,然后以低至1°C min -1 ...

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