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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 > 無氨基酵母氮源[不含硫酸胺]

              產品展示

              無氨基酵母氮源[不含硫酸胺]

              點擊次數:21發布時間:2016/8/30 14:46:45

              無氨基酵母氮源[不含硫酸胺]

              更新日期:2018/4/2 11:32:30

              所 在 地:中國大陸

              產品型號:

              簡單介紹:無氨基酵母氮源[不含硫酸胺] 英文名稱:O Amino acid 規格:BR 包裝:100g 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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               無氨基酵母氮源[含硫酸胺]齊一生物銷售:0216034 8496;181214 53965;173021 04490

              是我公司重點推廣產品,我公司有專業的人員進行全程指導,請放心購買,發貨時均會附上質檢報告單.使用說明書和推薦用法用量,提供正規發票. 無氨基酵母氮源[含硫酸胺]齊一生物科技(上海)有限公司客服熱線:400-991-0197網址:www.qiyibio.com

              無氨基酵母氮源[不含硫酸胺]   英文名稱:O Amino acid   規格:BR   包裝:100g     

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              9240719       Cable Carrier, Capper, Elevator, AP        CNY                          

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              9240696       Fitting, Barbed, 1/4" ID tube, AP             CNY                          

              9243651       Comprehen Valid., QIAgility      """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.

               

              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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              280437  virotype BTV RT-PCR Kit (480)             CNY                          

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              9020584       Y-Belt, DML3000 320 Teeth            CNY                          

              9020594       Enclosure, DML3000         CNY                          

              9021006       Motor, Pipettor Y, DCU            CNY                          

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              9013275       Motor, gripper, handler T/L, BR3000              CNY                          

              9013269       Fitting, PA tubing M6x1, 2.25mm, (10)           CNY                          

              9013210       Cabling kit, moving, BR8000            CNY                          

              9013198       Tubing,pres.sen.con.auto vac,BR8000v1.00           CNY                           【無氨基酵母氮源[不含硫酸胺]

              9013188       Valve set, pressure relaese, dispenser,             CNY                          

              9011730       Cable, level sensor, BR8000             CNY                          

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