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齐一生物科技(上海)有限公司是一家专业销售生化检测试剂盒.酶联免疫试剂盒,抗体蛋白.生化试剂,标准品和对照品的大型化学科技公司.自公司成立以来,本着始终拥有的创业激情,公司的销售额保持高速增长,企业规模不断扩大. 【鲁米诺CAS:521-31-3】齐一生物科技(上海)有限公司全国热线:400-991-0197网址:www.qiyibio.com
"鲁米诺CAS:521-31-3 英文名称:Luminol 规格:BR,98%,有害品 包装:1克 熔点: ≥300°C
比重: 1·433
储存条件: RT,避光
溶解性: 易溶于碱液,能溶于稀酸,不溶于水和有机溶剂,难溶于醇。中性或淡酸性溶液暴露在紫外光中时,显强烈的亮蓝色荧光。
用途: 发光测试: Emmax 440 nm (化学发光; 60 mM K2S2O8, 100 mM K2CO3, pH 11·5; 添
敏感性: 对空气敏感
介绍: 鲁米诺是一种最古老的和最常用的试剂,在碱性条件下可被过氧化物氧化,同时发光,鲁米诺和过氧化物之间的氧化还原反应需要催化剂,这种催化剂一般为多价金属离子、过氧化物酶如铁、辣根过氧化物酶等,此种方法常用于检测过氧化物、重金属、过氧化物酶的含量,以及由此衍生的检测自由基、进行毒物分析和基于过氧化物酶和葡萄糖氧化酶的分析方法。在通常情况下鲁米诺与过氧化氢在某些催化剂存在时化学发光反应非常迅速。最常用催化剂是金属离子,在很大浓度范围内,金属离子浓度与发光强度成正比,从而可进行某些金属离子的化学发光分析,利用这一反应可以分析那些含有金属离子的有机化合物,达到很高的灵敏度。其次是利用有机化合物对鲁米诺化学发光反应的抑制作用,测定对化学发光反应具有猝灭作用的有机化合物。其三是通过偶合反应间接测定无机或有机化合物。"
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9243654 Comprehen Valid., Other Quant. Sys. """The Comprehensive Validation Support plan specific to a laboratory's needs will incorporate all of the requirements for the internal validation guidelines from the FBI's Quality Assurance Standards (QAS).
The Comprehensive Validation Support service includes all travel and labor charges for up to 20 days by the QIAGEN Validation Team. Typically, one week will be required to extract, quantify, and amplify the validation study samples and may require multiple individuals. Usually, two weeks is required to analyze the data and one week to write the final report. The expected time period to complete the Comprehensive Validation is six weeks. The actual time may vary depending on resource availability, including laboratory time dedicated to validation activities.
Lab Work – The QIAGEN specialist(s) will travel to the laboratory to conduct the on-site validation lab work. The QIAGEN specialist team will perform and complete all extractions, quantifications, amplfications, and capillary electrophoresis. The laboratory is responsible for providing systems/protocols that may be needed (generally laboratory SOPs, ex. interpretation guidelines). Additionally, the laboratory staff may be required to provide additional data needed for interpretation (ex. quantification/amplification/CE results) during the data review phase of the validation.
Once the final scope of the validation is determined, QIAGEN will provide a quote for all consumables required for the validation. Non-QIAGEN chemistry and accessories are not included and should be purchased to cover the validation experimental design including qPCR, STR, NIST standards, required samples types (blood, semen, buccal samples) and required substrates (swabs, materials, etc). For planning purposes and to ensure a smooth process, the Customer is expected to have all materials on-hand and inventoried one (1) week prior to the validation start date.
Data Analysis – The Comprehensive Validation Support plan encompasses data collection (quants, amps, CE) during the on-site visit. The laboratory may be responsible for sharing (typically electronically via e-mail) any validation data requested after the on-site visit. A QIAGEN specialist will complete all of the data analysis produced from the validation study design. This includes qPCR (quant) and STR (amp) analysis and linkage to starting samples.
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