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药品、试剂常见规格标准索引
管理规范 ICH  人用药品注册技术要求国际协调会 GSP  药品经营企业管理规范 GMP  药品生产质量管理规范 GLP   药品非临床研究质量管理规范 GAP  中药材生产质量管理规范 GCP  药品临床试验管理规范 GPP  医疗机构制剂配制质量管理...[查看]
http://cxbio.com/Article/470_1.html
BioPorto2011产品目录
BioPorto发布了2011产品目录,包括了 The NGAL Test?, ELISA kits - NGAL, APC-PCI, MBL and 特有的AntibodyShop 组合。电子版本可以在以下地址下载:http://ipaper.ipapercms.dk/BioPorto/Productoverview2011/    [查看]
http://cxbio.com/Article/456_1.html
酶底物等色原
此反应首先由Trinder于1969年提出,故名Trinder反应。其原理为被测物质通过酶作用产生的过氧化氢(H2O2)在4-氨基替比林(4-AAP)、过氧化物酶(POD)的存在下,使色原物质可生成红色醌亚胺化合物。起初使用苯酚作生色剂,后来有许多种化合物替代苯酚,使反应的灵敏度得以显著提高。Trinder反应构成了葡萄糖、胆固醇、甘油三脂及尿酸等酶法测定的基础。[查看]
http://cxbio.com/Article/434_1.html
急性肾功能损伤早期检测NGAL快速酶联免疫试剂盒
NGAL快速酶联免疫试剂盒 NGAL Rapid ELISA Kit 可以在标准实验室使用常见的酶联免疫设备检测检测尿液、血清或血浆样本[查看]
http://cxbio.com/Article/NAGL_Rapid_ELISA_KIT_1.html
ELISA实验质量控制问题
  从1949年美国College of American Pathologists(简称CAP)首先开始研究临床实验室室内质量控制(简称质控)问题,美国学者Levery和Jenning于1950年发表了一篇关于使用质控图的实验室室内质控,临床检验实验室的室内质控工作正式拉序幕。 到70年代,实验室质量控制进入一个新的阶段--质量管理,推行Good Laboratory Parctice(简称GLP)。进入80年代末期,GLP的统一标准产生了,发展到\"认证实验室\"管理阶段。[查看]
http://cxbio.com/Article/353_1.html
Seebio诊断试剂生产原料、试剂、酶等促销
西宝生物科技(上海)股份有限公司(前身API Inc.成立于1999年),于2003年迁至上海更名成立,并已取得“西宝”注册商标。公司开展有进出口和国内业务,国内业务专注于诊断试剂、疫苗等生产企业提供生产原料和试剂,同时提供生命科学领域的试剂、仪器、耗材等。 在迎龙年之际,诊断试剂生产原料、试剂、酶等火热促销中,国内现货 货号 品名 促销价 大包装 纯度/备[查看]
http://cxbio.com/Article/299_1.html
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