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艾美捷科技特约代理Biogems产品。


BioGems意为生物钻石,其产品涵盖多种荧光标记的流式抗体、具有生物活性的功能性抗体,以及流式细胞术辅助试剂,如溶血剂和破膜剂等。BioGems产品全部在美国生产,目前已拥有超过500种流式试剂和600余种重组蛋白产品。

 

Through the establishment of joint collaborations with reputable manufacturers of top-quality life-science research products such as PeproTech Inc., BioGems has positioned itself to become a highly competitive source for a wide-range of recombinant protein and flow-cytometry reagents. Currently, our catalog contains more than 600 recombinant proteins and over 500 flow cytometry reagents. To keep up with the rapidly advancing research fronts, BioGems continuously adds new products to its catalog. All of our products are subjected to a thorough and rigorous quality and performance testing to ensure that each and every product meets the highest established standards. Providing our customers with the highest-quality products at affordable prices is our goal. We are confident that the unique business arrangements of BioGems together with our highly skilled and experienced personnel will enable us to achieve this goal.

 

主要产品分类:

(1)Flow Cytometry

Conjugated Antibodies

SAFIRE Functional Antibodies

Isotype Controls

Custom and Bulk Reagents

Purified Antibodies

Buffers and Solutions

(2)Recombinant Proteins

Growth Factors & Cytokines

Animal-Free Cytokines

Chemokines

Neurotrophins

Other Proteins

Anti Cytokine & Chemokine Antibodies

(3)Small Molecules

Receptor Antagonist and Inhibitors

Receptor Agonists and Activators

(4)Pre-Coated Elisa Kits

Human

Mouse

Rat

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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页面.png


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



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