世界*实验材料供应商Abraxis上海金畔生物为其中国代理，Abraxis 在一直是行业的*,一直为广大科研客户提供zui为的产品和服务,上海金畔生物一直秉承为中国科研客户带来的产品，的服务， Abraxis 就是为了给广大科研客户带来更加完善的产品和服务,您的满意将是我们zui大的收获

Abraxis 中国代理，Abraxis 上海代理，Abraxis北京代理， Abraxis 广东代理，Abraxis 江苏代理 Abraxis 湖北代理, Abraxis 天津, Abraxis 黑龙江代理, Abraxis内蒙古代理, Abraxis 吉林代理, Abraxis 福建代理, Abraxis 江苏代理, Abraxis 浙江代理, Abraxis 四川代理,

近20年来，Abraxis一直致力于研发，生产和销售快速的环境，食品和生命科学测试系统，包括免疫化学产品和方法，以满足研究和工业的测试需求。我们不断与政府，行业和学术合作，开发创新的方法和应用。当新的威胁（例如有害的藻华，三聚氰胺，食物中的草甘膦）出现时，这使得我们能够快速响应客户的分析要求。我们的许多产品都经过美国环保局，美国农业部，美国地质调查局，美国食品和药物管理局，日本环境部和世界卫生组织等机构的验证/验证。Abraxis拥有多个关键技术，或者是*许可证持有者，还有其他应用正在进行中。

我们的科学人员具有医疗，工业和环境检测方面的经验。我们能够定制程序，以具有竞争力的价格和高质量标准满足客户的特定需求。Abraxis总部位于美国，直接或通过分销商在100多个国家为我们的客户提供服务。

Vomitoxin (Deoxynivalenol, DON), ELISA Kits

呕吐毒素（脱氧雪腐镰刀菌烯醇，DON），ELISA试剂盒

货号：PN 53016B

INTENDED USE

The Abraxis Deoxynivalenol (DON) Plate Kit is a competitive ELISA for the quantitative analysis of vomitoxin in wheat, barley, malted barley, corn and oats. 

ASSAY PRINCIPLES

The Abraxis DON Plate Kit is a competitive enzyme-labeled immunoassay. DON is extracted from a ground sample by shaking with water. The aqueous extract is then filtered and the extract is tested in the immunoassay. DON-HRP enzyme conjugate is pipetted into the test wells followed by calibrators or sample extracts. DON antibody is then pipetted into the test wells to initiate the reaction. During the 10 minute incubation period, DON from the sample and DON-HRP enzyme conjugate compete for binding to DON antibody which, in turn, binds to the test well. Following this 10 minute incubation, the contents of the well are removed and the wells are washed to remove any unbound toxin or enzyme-labeled toxin. A clear substrate is then added to the wells and any bound enzyme-toxin conjugate causes the conversion to a blue color. Following a 5 minute incubation, the reaction is stopped and amount of color in each well is read. The color of unknown samples is compared to the color of the calibrators and the DON concentration of the samples is derived. 

世界*实验材料供应商Abraxis上海金畔生物为其中国代理，Abraxis 在一直是行业的*,一直为广大科研客户提供zui为的产品和服务,上海金畔生物一直秉承为中国科研客户带来的产品，的服务， Abraxis 就是为了给广大科研客户带来更加完善的产品和服务,您的满意将是我们zui大的收获

Abraxis 中国代理，Abraxis 上海代理，Abraxis北京代理， Abraxis 广东代理，Abraxis 江苏代理 Abraxis 湖北代理, Abraxis 天津, Abraxis 黑龙江代理, Abraxis内蒙古代理, Abraxis 吉林代理, Abraxis 福建代理, Abraxis 江苏代理, Abraxis 浙江代理, Abraxis 四川代理,

近20年来，Abraxis一直致力于研发，生产和销售快速的环境，食品和生命科学测试系统，包括免疫化学产品和方法，以满足研究和工业的测试需求。我们不断与政府，行业和学术合作，开发创新的方法和应用。当新的威胁（例如有害的藻华，三聚氰胺，食物中的草甘膦）出现时，这使得我们能够快速响应客户的分析要求。我们的许多产品都经过美国环保局，美国农业部，美国地质调查局，美国食品和药物管理局，日本环境部和世界卫生组织等机构的验证/验证。Abraxis拥有多个关键技术，或者是*许可证持有者，还有其他应用正在进行中。

我们的科学人员具有医疗，工业和环境检测方面的经验。我们能够定制程序，以具有竞争力的价格和高质量标准满足客户的特定需求。Abraxis总部位于美国，直接或通过分销商在100多个国家为我们的客户提供服务。

霉菌毒素是由在人类和动物食品中生长的真菌产生的，并且会引起严重的影响，如呕吐，器官衰竭，癌症和死亡。Abraxis提供检测和测量这些重要毒素的试剂盒。

Zearalenone Plate Kit 

货号：PN 53018B

INTENDED USE

The Abraxis Zearalenone Plate Kit is a competitive ELISA for the quantitative analysis of zearalenone in corn, corn meal, corn germ meal, corn gluten meal and corn/soy blend. 

ASSAY PRINCIPLES

The Abraxis Zearalenone kit is a competitive enzyme-labeled immunoassay. Zearalenone is extracted from a ground sample by shaking with methanol/water. The extract is then filtered and diluted, the extract is then tested in the immunoassay. Zearalenone-HRP enzyme conjugate is pipetted into mixing wells followed by calibrators or sample extracts. The sample-HRP mixture is then pipetted into the test wells to initiate the reaction. During the 10 minute incubation period, zearalenone from the sample and zearalenone-HRP enzyme conjugate compete for binding to zearalenone antibody which, in turn, binds to the test well. Following this 10 minute incubation, the contents of the well are removed and the wells are washed to remove any unbound enzyme-labeled toxin. A clear substrate is then added to the wells and any bound enzyme-toxin conjugate causes the conversion to a blue color. Following a 5 minute incubation, the reaction is stopped and amount of color in each well is read. The color of unknown samples is compared to the color of the calibrators and the Zearalenone concentration of the samples is derived.