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艾美捷科技代理Imanis Life Sciences品牌全系列产品


Imanis Life Sciences是一家专注于再生医学、基因治疗、肿瘤学及溶瘤病毒疗法研究领域的生物技术公司。Imanis Life Sciences科研领域提供两大核心解决方案:溶瘤病毒治疗研究产品:供应用于溶瘤病毒疗法研究的专用病毒制剂;非侵入性影像检测试剂:提供适用于体外及体内研究的全系列试剂,包括报告基因细胞系、报告基因慢病毒载体及特异性抗体。Imanis Life Sciences公司的产品主要包括高品质报告基因细胞系、慢病毒载体及基因构建体、NIS与VSV特异性抗体以及全系列溶瘤病毒资源库。


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▍Imanis Life Sciences产品线

● 报告基因慢病毒载体与质粒体系:提供全系列报告基因慢病毒载体及配套质粒解决方案。

即用型病毒载体:安全高效的即用颗粒,适用于原代细胞等难转染细胞类型的报告基因递送(无需额外处理);

病毒包装质粒系统:用于自主制备慢病毒载体颗粒的完整质粒体系。

● 稳定细胞系产品线:提供支持肿瘤学及免疫肿瘤学体内外研究的全系列稳定细胞系。

组成型报告基因细胞系(持续表达):搭载荧光素酶、荧光蛋白或NIS报告基因。应用于体外药物筛选 / 活体动物肿瘤动态监测

肿瘤抗原工程细胞系(靶标调控型):经基因编辑调控常见肿瘤相关抗原及治疗靶点表达水平,核心靶标:CD19、EGFR、Her2

● 溶瘤病毒资源库:提供涵盖即用型病毒储备的完整解决方案,全面助力溶瘤病毒疗法的体内外研究进程。

● 抗体:提供优质的NIS抗体产品,全面兼容免疫印迹(WB)、免疫组化(IHC)、免疫荧光(IF)、流式细胞术,同时推出多功能抗VSV(水泡性口炎病毒)抗体,覆盖WB/IHC/IF/ELISA/流式及VSV中和实验全平台。


▍Imanis Life Sciences部分产品列表


品名规格货号
V-pNIS0.25 mL;1.0 mLLV053S;LV053L
LV-Ub-humanNIS-P2A-Puro0.25 mL;1.0 mLLV038S;LV038L
LV-PGK-humanNIS-P2A-Puro0.25 mL;1.0 mLLV036S;LV036L
LV-humanNIS-P2A-Puro0.25 mL;1.0 mLLV019S;LV019L
LV-humanNIS-IRES-Neo0.25 mL;1.0 mLLV013S;LV013L
LV-humanNIS0.25 mL;1.0 mLLV001S;LV001L
LV-EF1α-humanNIS-P2A-Puro0.25 mL;1.0 mLLV037S;LV037L
LV-CAG-humanNIS-P2A-Puro0.25 mL;1.0 mLLV042S;LV042L
LV-rhesusNIS-PGK-Puro0.25 mL;1.0 mLLV018S;LV018L
LV-rhesusNIS0.25 mL;1.0 mLLV017S;LV017L
LV-EF1α-rhesusNIS-PGK-Puro0.25 mL;1.0 mLLV040S;LV040L
LV-mouseNIS-P2A-Neo0.25 mL;1.0 mLLV025S;LV025L
LV-mouseNIS-PGK-Puro0.25 mL;1.0 mLLV022S;LV022L
Anti-human NIS antibody SJ10.25 mlREA004
Monoclonal anti-human NIS antibody (affinity purified)100 ulREA011
Anti-human (KELE) NIS antibody (affinity purified)100 ulREA010
Anti-human (ETNL) NIS antibody (affinity purified)100 ulREA009
Anti-human NIS antibody clone VJ20.25mLREA003
Anti-human NIS antibody clone VJ10.25mLREA002
Anti-rat NIS antibody (affinity purified)100 ulREA008
Anti-VSV antibody0.25mLREA005



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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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