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苯甲基-2-磺酰三硝基三氮唑CAS:74257-00-4

點擊次數(shù):29發(fā)布時間:2016/8/29 23:03:05

苯甲基-2-磺酰三硝基三氮唑CAS:74257-00-4

更新日期:2018/4/2 11:32:30

所 在 地:中國大陸

產(chǎn)品型號:

簡單介紹:苯甲基-2-磺酰三硝基三氮唑CAS:74257-00-4 英文名稱:MSNT 規(guī)格:AR,99% 包裝:5克 齊一生物科技(上海)有限公司銷售:021-6034 8496;181214 53965;173021 04490

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 苯甲基-2-磺酰三硝基三氮唑CAS:74257004齊一生物銷售:0216034 8496;181214 53965;173021 04490

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"苯甲基-2-磺酰三硝基三氮唑CAS:74257004   英文名稱:MSNT   規(guī)格:AR,99%   包裝:5      熔點: 132134°C

比重: 1·51

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用途: 合成寡核苷酸的試劑

介紹: 常溫易分解。"

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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.

 

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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.

 

Validation data CD/flashdrive – QIAGEN will review the validation data and draft a validation summary document, ensuring compliance with the FBI's QAS requirements/standards. QIAGEN will send validation data in an electronic format (email/CD/flashdrive) to the laboratory. The laboratory is responsible for final compilation, any format change preferences, review and signoff of the validation report. The documentation provided by QIAGEN will aide in demonstrating compliance with all accreditation guidelines during laboratory audits. Should a hard copy of the validation study be preferred, the laboratory is required to specify prior to the onset of the validation.

 

Post-validation QIAGEN-to-Laboratory Transfer – Following completion of the validation and generation of the draft validation summary document, a designated member of the QIAGEN validation team will review the validation with the Lab Manager and the Technical Leader. Following sign off on the validation report, training of the laboratory DNA staff will occur. Refer to the Post-validation Competency Training for additional information. """ CNY                          

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