{{'Search' | translate}}
 

L-Glutamine

100ML L-谷氨酰胺(200mM)

Company: Thermo Fisher Scientific
Catalog#: 25030024
Bio-protocol()
Company-protocol()
Other protocol()

Assessing the Efficacy of Small Molecule Inhibitors in a Mouse Model of Persistent Norovirus Infection
Author:
Date:
2018-05-05
[Abstract]  Human norovirus is the most common cause of acute gastroenteritis worldwide, resulting in estimated mortality of ~210,000 each year, of whom most are children under the age of five. However, norovirus can infect people of all age groups. There is a risk of prolonged infection in children, the elderly and patients who are immunocompromised. To study the inhibition of persistent norovirus replication by small molecule antivirals in vivo, we used a murine norovirus CR6 strain (MNV.CR6). We demonstrated earlier that efficient small molecules can reduce viral shedding in the stool of infected mice. Here we present how to generate the MNV.CR6 virus stock, infect type I and II interferon receptor knockout AG129 mice via oral gavage, administer antivirals to mice, and quantify viral ... [摘要]  人类诺瓦克病毒是全球急性胃肠炎最常见的原因,估计每年约有210,000人死亡,其中大部分是5岁以下的儿童。 然而,诺如病毒可以感染所有年龄组的人。 儿童,老年人和免疫功能低下的患者有长期感染的风险。 为研究体内小分子抗病毒剂对持续诺如病毒复制的抑制作用,我们使用鼠诺沃克病毒CR6株(MNV.CR6)。 我们之前表明,高效小分子可以减少感染小鼠粪便中的病毒脱落。 在这里,我们介绍如何产生MNV.CR6病毒,通过口服灌胃感染I型和II型干扰素受体敲除AG129小鼠,给小鼠施用抗病毒药物,并量化这些小鼠粪便中的病毒基因组拷贝。

【背景】人诺瓦克病毒是胃肠炎的重要原因。尽管大多数诺罗病毒感染是急性和自限性的,但是在具有免疫缺陷状态的患者中,尤其是在实体器官和造血干细胞移植受体,接受化疗的患者和患有AIDS的患者中,感染可能变成慢性的(Westhoff等人, / em>,2009; Green,2014; Angarone 等。,2016)。在幼儿和老年人中也观察到延长的诺如病毒感染,导致疾病持续时间增加,排便增加和病毒脱落长达47天(Murata等人,2007; ...

An Affinity-directed Protein Missile (AdPROM) System for Targeted Destruction of Endogenous Proteins
Author:
Date:
2017-11-20
[Abstract]  We recently reported an Affinity-directed PROtein Missile (AdPROM) system for the targeted proteolysis of endogenous proteins of interest (POI) (Fulcher et al., 2016 and 2017). AdPROM consists of the Von Hippel Lindau (VHL) protein, a Cullin 2 E3 ligase substrate receptor (Bosu and Kipreos, 2008), conjugated to a high affinity polypeptide binder (such as a camelid nanobody) that recognises the target protein in cells. When introduced in cells, the target protein is recruited to the CUL2 E3 ubiquitin ligase complex for ubiquitin-mediated proteasomal degradation. For target protein recruitment, we have utilised both camelid-derived VHH domain nanobodies as well as synthetic polypeptide monobodies based on the human type III fibronectin domain (Sha et al., 2013; Fridy et ... [摘要]  我们最近报道了一种针对内源性感兴趣蛋白(POI)的靶向蛋白水解的亲和指导PROtein导弹(AdPROM)系统(Fulcher等人,2016和2017)。 AdPROM由Von Hippel Lindau(VHL)蛋白组成,Cullin 2 E3连接酶底物受体(Bosu and Kipreos,2008),与识别细胞中靶蛋白的高亲和力多肽结合剂(如骆驼科纳米抗体)缀合。当在细胞中引入时,靶蛋白质被招募到CUL2 E3泛素连接酶复合体用于泛素介导的蛋白酶体降解。对于靶蛋白的募集,我们使用了基于人类III型纤连蛋白结构域的骆驼科动物来源的VHH结构域纳米抗体以及合成多肽单体(Sharm等人,2013; Fridy等人。,2014; Schmidt et al。,2016)。在此协议中,我们描述了生成AdPROM构建体及其在人细胞系中用于靶蛋白质破坏的详细方法。 AdPROM允许对POI进行功能表征,并且其目标蛋白质破坏的效率克服了RNA干扰方法的许多局限性,这些方法需要长时间的治疗并与脱靶效应相关联,而CRISPR / Cas9基因编辑并不总是可行的。
【背景】该协议使人们能够在哺乳动物细胞系中设计,构建和表达AdPROM VHL-nano ...

Isolation and Cultivation of Primary Brain Endothelial Cells from Adult Mice
Author:
Date:
2017-05-20
[Abstract]  Brain endothelial cells are the major building block of the blood-brain barrier. To study the role of brain endothelial cells in vitro, the isolation of primary cells is of critical value. Here, we describe a protocol in which vessel fragments are isolated from adult mice. After density centrifugation and mild digestion of the fragments, outgrowing endothelial cells are selected by puromycin treatment and grown to confluence within one week. [摘要]  脑内皮细胞是血脑屏障的主要组成部分。 为了研究脑内皮细胞在体外的作用,原代细胞的分离是临床价值。 在这里,我们描述了一种方案,其中血管片段与成年小鼠分离。 在密度离心和片段的温和消化后,通过嘌呤霉素处理选择出生长的内皮细胞,并在一周内生长至汇合。
【背景】血脑屏障保护大脑免受细胞和物质的不受控制的侵入。 这主要是由脑内皮细胞形成的屏障组成的紧密和粘附连接限制细胞旁运输。
该方案被开发以克服维持其关键特征的小鼠脑内皮细胞系的有限可用性,例如表达足够量的紧密连接蛋白如闭合蛋白,ZO-1或紧密连接蛋白-5以诱导高跨内皮细胞抗性。
此外,从内含基因修饰的小鼠中分离脑内皮细胞可以在体外研究基因特异性功能。
使用这种方法,我们以前补充了体内研究,证明NF-κB信号在脑内皮细胞中维持正常血脑屏障功能的重要性(Ridder等,2015)。

Comments