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37 °C and 5% CO2 cell culture incubator

37℃和5%CO 2细胞培养箱

Company: WAKENBTECH
Catalog#: 9000EX
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In vitro Treatment of Mouse and Human Cells with Endogenous Ligands for Activation of the Aryl Hydrocarbon Receptor
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Date:
2017-01-05
[Abstract]  Activation of the aryl hydrocarbon receptor (AHR) by endogenous ligands has been implicated in a variety of physiological processes such as cell cycle regulation, cell differentiation and immune responses. It is reported that tryptophan metabolites, such as kynurenine (Kyn) and 6-formylindolo(3,2-b)carbazole (FICZ), are endogenous ligands for AHR (Stockinger et al., 2014). This protocol is designed for treatment with Kyn or FICZ in mouse embryonic fibroblasts (MEFs) or primary peripheral monocytes. [摘要]  通过内源性配体活化芳基烃受体(AHR)已涉及多种生理过程,如细胞周期调控,细胞分化和免疫应答。据报道,色氨酸代谢物,如犬尿胆碱(Kyn)和6-甲基吲哚(3,2-b)咔唑(FICZ)是AHR的内源性配体(Stockinger等人,2014)。该方案设计用于在小鼠胚胎成纤维细胞(MEF)或初级周边单核细胞中用Kyn或FICZ进行治疗。

背景 色氨酸代谢物如Kyn和FICZ是生理条件下AHR的内源性配体。 Kyn由色氨酸-2,3-双加氧酶(TDO)和/或吲哚胺-2,3-双加氧酶1和2(IDO1 / 2)产生,并有助于抑制抗肿瘤反应和恶性进展(Stockinger等人,2014)。 ...

HBV Infection in Human Hepatocytes and Quantification of Encapsidated HBV DNA
Author:
Date:
2016-01-20
[Abstract]  Human hepatic cancer cell lines such as HepG2, Huh7, and HLE cannot get infected with Hepatitis B virus (HBV) due to lack of an HBV receptor(s). Transfection with HBV genome has so far been referred as a tool to mimic HBV infection. However, since sodium taurocholate cotransporting polypeptide (NTCP) was identified as a functional receptor for HBV (Yan et al., 2012), hepatocyte cell lines that were stably transfected with a plasmid for NTCP expression have been used for HBV infection. This protocol is designed for infection with HBV in human hepatocyte cell line HepG2 expressing NTCP (HepG2-hNTCP-C4 cells; Iwamoto et al., 2014) or primary human hepatocytes (PHHs). In this section, we also describe one of the methods for the assessment of HBV infection: Quantification of ... [摘要]  人肝癌细胞系如HepG2,Huh7和HLE由于缺乏HBV受体而不能感染乙型肝炎病毒(HBV)。 HBV基因组的转染迄今为止被称为模拟HBV感染的工具。 然而,由于牛磺胆酸钠共转运多肽(NTCP)被鉴定为HBV的功能性受体(Yan等人,2012),已经使用用用于NTCP表达的质粒稳定转染的肝细胞细胞系 为HBV感染。 该方案设计用于在表达人类肝细胞细胞系HepG2的表达NTCP(HepG2-hNTCP-C4细胞; Iwamoto等人,2014)或原代人肝细胞(PHH)的HBV感染。 在本节中,我们还描述了用于评估HBV感染的方法之一:细胞内衣壳化的HBV DNA的定量。

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