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              您的位置:易推廣 > 化工原料 > 化學試劑 > 生化試劑 > 齊一生物科技(上海)有限公司 > 產品展示 > 生化試劑盒 > 生化檢測試劑 > HIV-1 Protease Activity Assay Kit (Fluorometric)

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              HIV-1 Protease Activity Assay Kit (Fluorometric)

              點擊次數:31發布時間:2016/7/28 22:39:38

              HIV-1 Protease Activity Assay Kit (Fluorometric)

              更新日期:2016/7/28 22:39:38

              所 在 地:中國大陸

              產品型號:

              簡單介紹:HIV-1 Protease Activity Assay Kit (Fluorometric) 貨號K825-100 100 assays 美國 Biovision進口,齊一生物代理,部分產品現貨供應

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               HIV-1 Protease Activity Assay Kit (Fluorometric)齊一生物專業經營銷售通用試劑.分析試劑.標準物質.合成試劑.中間體.催化劑.生化試劑等化學產品,我們致力于以專業化的視角,提供豐富專業產品資料及其相關技術開發資訊,產品內容覆蓋分析化學.無機化學.有機化學.生命科學.材料科學等領域. HIV-1 Protease Activity Assay Kit (Fluorometric)已迅速發展成為國內科學試劑的運營商,是國家重點實驗室指定供應商,并與國內多家科研單位緊密合作. 齊一生物銷售:0216034 8496;181214 53965;173021 04490網站:http://www.qiyibio.com

               

              HIV-1 Protease Activity Assay Kit (Fluorometric)齊一生物科技(上海)有限公司經營試劑種類眾多:覆蓋分析化學品,無機化學品,有機化學品,生物化學品,材料化學品等.試劑信息齊全:包含試劑特性描述,詳細質量信息,應用方法.標準科研 用途以及正在開發的前沿應用歡迎前來選購。齊一生物銷售:0216034 8496;181214 53965;173021 04490網站:http://www.qiyibio.com

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              9243653  Comprehen Valid., Other Extraction 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).   The Customer is expected to have all materials on-hand 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.

               

              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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