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DMEM, high glucose, GlutaMAXTM, pyruvate

DMEM, high glucose, GlutaMAXTM Supplement, pyruvate

Company: Thermo Fisher Scientific
Catalog#: 10569044
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Generation and Implementation of Reporter BHK-21 Cells for Live Imaging of Flavivirus Infection
Author:
Date:
2021-03-05
[Abstract]  

The genus Flavivirus within the family Flaviviridae includes many viral species of medical importance, such as yellow fever virus (YFV), Zika virus (ZIKV), and dengue virus (DENV), among others. Presently, the identification of flavivirus-infected cells is based on either the immunolabeling of viral proteins, the application of recombinant reporter replicons and viral genomes, or the use of cell-based molecular reporters of the flaviviral protease NS2B-NS3 activity. Among the latter, our flavivirus-activatable GFP and mNeptune reporters contain a quenching peptide (QP) joined to the fluorescent protein by a linker consisting of a cleavage site for the flavivirus NS2B-NS3 proteases (AAQRRGRIG). When the viral protease cleaves the linker, the quenching peptide is removed, and the

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[摘要]  [摘要]本属黄病毒家族中的黄病毒包括医学重要性许多病毒种类,如黄热病病毒(YFV),寨卡病毒(ZIKV)和登革热病毒(DENV),等等。目前,黄病毒感染细胞的鉴定是基于病毒蛋白的免疫标记,重组报告子复制子和病毒基因组的应用,或黄病毒蛋白酶NS2B-NS3活性的基于细胞的分子报告子的使用。在后者中,我们的黄病毒可激活的GFP和mNeptune报道分子含有通过接头连接到荧光蛋白的淬灭肽(QP),该接头由黄病毒NS2B - NS3蛋白酶(AAQRRGRIG)的切割位点组成。当病毒蛋白酶切割接头时,淬灭肽被去除,并且荧光蛋白采用促进荧光的构象。在这里,我们提供了用于表达,选择和实施表达黄病毒基因编码分子报告子的稳定BHK-21细胞的详细协议,适用于通过活细胞成像监测病毒感染。我们还将描述图像分析过程并提供所需的软件管道。我们的报告细胞允许通过活细胞成像对黄病毒的参考菌株和天然菌株实施单细胞感染动力学以及噬菌斑测定。

图形摘要:

黄病毒感染实时成像的报告基因BHK-21细胞的产生与实施工作流。


[背景]黄病毒代表了正在引起并正在重新出现的全球性威胁,可能引起动物和人类疾病,包括许多与医学有关的病毒,例如黄热病病毒(YFV),西尼罗河病毒(WNV),日本脑炎病毒(JEV),登革热病毒(DENV),并兹卡六RUS(ZIKV),等等(摹·乌尔德·所罗门,2008) ...

Reconstruction of the Mouse Inflammasome System in HEK293T Cells
Author:
Date:
2016-11-05
[Abstract]  The NLRP3 (NLR family, Pyrin domain containing 3) inflammasome is a multiprotein complex comprised of NLRP3, pro-caspase-1, the adaptor protein apoptosis-associated speck-like protein containing a CARD (ASC), and the protein kinase NIMA related kinase 7 (NEK7) (Shi et al., 2016; He et al., 2016; Schmid-Burgk et al., 2016). When cells are exposed to microbes and/or danger signals, the inflammasome assembles and serves as a platform for the activation of caspase-1. Caspase-1 activation promotes the processing and secretion of the pro-inflammatory cytokines interleukin-1β (IL-1β), IL-18, and IL-33 as well as pyroptosis induction (Gross et al., 2011; Arend et al., 2008), which elicit inflammatory responses. Here, we describe how to co-transfect the ... [摘要]  核糖体足迹或Ribo-seq,彻底改变了翻译研究。它最初是为培养中的酵母和哺乳动物细胞开发的(Ingolia等人,2009)。本文中,我们描述了来自先前公开的多核糖体分离程序的植物优化的亲手核糖体印迹方案(Ingolia等人,2009; Mustroph等人,2009 )和核糖体印迹(Ingolia等人,2009; Ingolia等人,2013)。使用该协议,我们能够成功地分离和分析来自体外生长的拟南芥植物(黑暗生长的幼苗)的不同阶段的高质量核糖体印迹[Merchante < ,以及在液体培养物中生长的板和植物中的13天龄小植物[未发表的结果])。

[背景] 翻译在调节基因活性中的中心作用早已被公认,但是在响应于特定刺激的全基因组翻译定量变化的系统探索最近才变得技术上可行。最初为培养中的酵母和哺乳动物细胞开发的核糖体印迹技术(通常称为Ribo-seq)已经彻底改变了翻译调节和基因表达的研究,因为其允许确定核糖体在基因组 - ...

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