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艾美捷科技代理NanoLight Technology品牌。

NanoLight Technology公司致力于开发天然发光海洋蛋白(海洋生物发光)的应用。NanoLight® 技术的生命科学应用包括:高通量药物发现、功能基因组学、肿瘤成像、放射性同位素替代、光遗传学、分子诊断等。自2012年以来,NanoLight Technology公司主要提供无毒、水溶性的生物发光底物,用于体内成像领域,以监测小鼠模型中的肿瘤生长。另一个非常新的应用是光遗传学领域,它为神经科学家提供了使用生物发光控制神经元的惊人能力。NanoLight Technology公司研究团队不断扩大产品组合。Prolume Purple(美国专利 9,624,425),是一种新型底物,其性能优于广泛用于研究蛋白质-蛋白质相互作用的 DeepBlueC™。除了基本的生物发光化合物外,NanoLight 还将这些底物整合到复杂的缓冲系统中,适用于具有不同动力学特性的各种荧光素酶,为研究人员提供便利,并为制药公司的自动化高通量筛选提供可靠的批次控制试剂。NanoLight 也是开发分子靶标传感工具的领导者。NanoLight 提供迄今为止已知的两种最亮荧光素酶——高斯荧光素酶(GLuc-SA)和 Oplophorous 荧光素酶(NLuc-SA)的链霉亲和素偶联物,便于检测生物素化分子(如 DNA、RNA、肽、蛋白质)。

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艾美捷科技代理NanoLight Technology品牌
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Dendritics.jpg

Dendritics公司主要关注人类树突状细胞,希望找到能够促使CD34+造血前体细胞转化为树突状细胞(在GM-CSF和TNF-alpha存在的情况下)的细胞因子。在1992-2005年间,大量的研究使得研究者对人类树突状细胞的产生、细胞通路、C-type凝集素受体的功能及Toll-like受体的活性有了更深的理解。

 

DENDRITICS was started in 2005 by former members of SCHERING PLOUGH Laboratory for Immunological Research (LIR) in Dardilly, France. From their long experience at LIR, the team members of DENDRITICS have gathered complementary scientific and technological knowledge in different areas of immunology. The initial focus of LIR was in the biology of B lymphocytes, elaboration of human monoclonal antibodies, and in cytokine discovery (IL-3, IL-4, IL-7, IL-10, IL-17, GM-CSF) together with our colleagues of DNAX Research Institute in Palo Alto, California.

 

Our interest in cytokines led to the finding that human dendritic cells (DCs) could be generated in vitro from CD34+ hematopoietic progenitors cultured in the presence of GM-CSF and TNF-alpha.

 

The period from 1992 to 2005 saw the specialization of LIR in DC biology and was fuelled by a large-scale effort to discover and study the function of genes specifically expressed by these cells. This program led to a number of findings that contributed in particular to understanding the heterogeneity of DCs, the pathways regulating DC migration, the function of C-type lectin receptors in DCs and the activity of Toll-like receptors in DCs. Many novel genes were discovered through screening of cDNA libraries or through monoclonal antibodies raised against DCs.

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