求解答: 进口试剂TFFluorogens直采,是正品吗?
苏州蚂蚁淘生物科技有限公司成立于2009年，是一家专业提供实验室整体采购方案的专业公司，为广大采购和实验室解决了大量问题，几年来已经成为几乎所有合作伙伴最优秀的合作伙伴，我们一直秉承信誉第一的原则，坚持不卖假货，哪怕利润损失也要为客户提供最好的产品。
我们已经和国外500多个品牌建立了贸易往来，并在国际上享有相当知名度，现已经成为国外近100个品牌中国指定代理，并成为其中国最优秀的代理商。
我们部分客户
1：经销商代表---国药化试，飞世尔，SIGMA，等1000家左右的经销商
2：学校代表---北京大学，清华大学，上海交通大学，复旦大学，浙江大学，武汉大学，厦门大学.....等200所左右大学及100多家附属医院
3：制药公司代表：罗氏，阿斯利康，诺和诺德，和记黄埔，东阳光科......
4：CRO公司代表：睿智化学，药明康德，桑迪亚，美迪西......
我们现有代理品牌如下，还在不断增加中
The Twinkle Factory labeling technology enables the specific fluorescent labeling of any protein of interest (POI). It is based on the instantaneous formation of a fluorescent molecular assembly between the small (14 kDa), genetically encoded, protein tag FAST and various fluorogenic ligands (TFFluorogens). TFFluorogens strongly fluoresce only when bound to FAST, enabling to detect and image FAST-tagged proteins with high contrast without the need of washing the excess of fluorogenic ligands. The labeling of FAST-tagged proteins with a TFFluorogen is non-covalent and can be reversed if necessary by washing. Furthermore, FAST does not require molecular oxygen for being fluorescent, unlike fluorescent proteins, enabling to fluorescently label proteins in weakly oxygenated or anaerobic environments, helpful for biofilm imaging, or for any anaerobe imaging, e.g., Clostridium.
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苏州蚂蚁淘生物科技有限公司SuZhouebiomall BIOLOGicalTechnologyCo.,Ltd.成立于2017年，经过数年的努力已迅速成为集科研和生产为一体的专业化生物工程公司。特别是ELISA研发，代测，技术服务这一产品已使苏州蚂蚁淘成为中国知名公司。公司产品涵盖ELISA研发、细胞培养，各种生化试剂、各种酶类、分子生物学试剂盒、培养基、自产实验室耗材、小型仪器等。此外、苏州蚂蚁淘还代理了美国药典标准品，中检所标准品，sigma,ScienCell,ATCC,wak0,omega，Worthington、MBI、Bioworld、Calendon等国外各类知名公司的产品。苏州蚂蚁淘将进一步加强人才经营、产品经营，不断提升企业的核心竟争力，实现具有高科技产业体系、知识化创业团队的国际化的公司，服务于生命科学领域，迎接世界经济一体化所带来的机遇与挑战。
全部回答 （共 2 条）
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The Twinkle Factory labeling technology enables the specific fluorescent labeling of any protein of interest (POI). It is based on the instantaneous formation of a fluorescent molecular assembly between the small (14 kDa), genetically encoded, protein tag FAST and various fluorogenic ligands (TFFluorogens). TFFluorogens strongly fluoresce only when bound to FAST, enabling to detect and image FAST-tagged proteins with high contrast without the need of washing the excess of fluorogenic ligands. The labeling of FAST-tagged proteins with a TFFluorogen is non-covalent and can be reversed if necessary by washing. Furthermore, FAST does not require molecular oxygen for being fluorescent, unlike fluorescent proteins, enabling to fluorescently label proteins in weakly oxygenated or anaerobic environments, helpful for biofilm imaging, or for any anaerobe imaging, e.g., Clostridium.
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