艾美捷科技代理Hybrid Plastics全系列倍半硅氧烷POSS化合物。

笼型倍半硅氧烷，具有无机立方核和外部有机基团的有机-无机杂化化合物。倍半硅氧烷是一种有机硅化合物，其化学式为[RSiO3/2]n（R=H，烷基，芳基或烷氧基）。倍半硅氧烷是无色固体，采用笼状或聚合结构，具有Si-O-Si键和四面体Si顶点。倍半硅氧烷是多八面体倍半硅氧烷（POSS）的一种，作为陶瓷材料和纳米复合材料的前驱体引起了人们的关注。不同的取代基（R）可以连接到Si中心。这些分子是不寻常的，因为它们具有无机硅酸盐核和有机表面。硅芯具有刚性和热稳定性。

Hybrid Plastics致力于提供全球最高质量的POSS®材料。具有ISO 9001:2008的质量管理体系，艾美捷科技有限公司与Hybrid Plastics Inc.长期合作，致力于为中国用户提供：Acrylates-POSS、Alcohols-POSS、Amines-POSS、Carboxylic Acids-POSS、Epoxides-POSS、Fluoroalkyls-POSS、Halides-POSS、Methacrylates-POSS、Molecular Silicas-POSS、Norbornenyls-POSS、Olefins-POSS、PEGs-POSS、Silanes-POSS、Silanols-POSS、Thiols-POSS等化合物。

 MA0736 Acryloxypropyl POSS Cage mixture  现货销售   

 MA0735 Methacryloxypropyl POSS 现货销售   

 AM0270 AminopropylIsooctyl POSS 现货销售 

产品主要包括：

http://www.amyjet.com/Index/lists/catid/27/kid/28.html

艾美捷科技代理Aneufast品牌全系列产品

Aneufast是一家专业生产诊断非整倍体染色体试剂盒的生物公司。QF-PCR试剂盒Aneufast公司的核心产品。Aneufast™ QF-PCR试剂盒包含六组多重标记系统，基于短串联重复序列（STRs）扩增技术，可同步检测精选微卫星位点及性别决定基因（Amelogenin-SRY）。该设计通过单次反应实现多染色体同步筛查，显著提升检测效率。此标记组合可精准识别13、18、21号常染色体及X、Y性染色体的非整倍体异常。

Aneufast™ QF-PCR试剂盒具有以下特点：

● 五色荧光DNA片段分析系统：采用五重荧光标记技术，实现单次电泳中13/18/21/X/Y染色体STR标记的同步检测与区分；

● 即用型PCR预混体系：含热启动聚合酶及优化缓冲液，操作仅需 "加DNA→扩增" 两步；

● 超快速检测流程：样本到结果仅需3.5小时

● 染色体特定位点备份设计：每套试剂盒额外提供 13/18/21/X/Y染色体专属STR标记（独立分装）

● 全平台兼容性：经优化适配ABI全系列基因分析仪，如3500/3500xL Dx，SeqStudio Flex和7500 Fast Dx

● 国际质量认证：符合欧盟体外诊断指令98/79/EC；通过 ISO 9001:2000 及 ISO 13485:2003 医疗器械生产双认证

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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