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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 > 變異鏈球菌ATCC35668

              產品展示

              變異鏈球菌ATCC35668

              點擊次數:38發布時間:2016/6/28 21:05:41

              變異鏈球菌ATCC35668

              更新日期:2016/6/28 21:05:41

              所 在 地:中國大陸

              產品型號:

              簡單介紹:變異鏈球菌ATCC35668 貨號:QT-00061 凍干粉

              相關標簽:變異鏈球菌ATCC35668 

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              詳細內容

               變異鏈球菌ATCC35668齊一生物科技(上海)有限公司檢測試劑盒產品已被廣泛應用于化學.化工.生命科學的基礎研究和開發應用.制藥.疾病診斷與控制.人口與健康.生物技術等諸多領域.客戶遍布國內各大學.研究所.醫院.衛生防疫.商品檢驗檢疫.制藥公司. 生物技術公司和食品工業等單位. 變異鏈球菌ATCC35668齊一生物銷售:0216034 8496;181214 53965;173021 04490網址:www.qiyibio.com

               

              變異鏈球菌ATCC35668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. 齊一生物銷售:0216034 8496;181214 53965;173021 04490網址:www.qiyibio.com

               

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              Service response time (repair): 48 hours/2 business days

              Periodic inspection/maintenance: yes, 1/agreement year

              Inspection/maintenance delivery: onsite

              Cost coverage for repair parts: yes, included

              Cost coverage for labor: yes, included

              Cost coverage for travel: yes, included

              Replacement system (Loaner) provision: not included

              Transportation cost coverage: not applicable"CNY

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              9241211Full Agreement Depot Repair, DML2000, 1y"The Full Agreement Depot Repair, DML2000 provides full service coverage for the DML 2000 luminometer. The service is conducted as an instrument exchange service. 

              All shipping, labor and repair part costs related to an instrument exchange are included for 1 year. Instrument exchange time is 2 - 3 working days."CNY

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              9243650Comprehen Valid., EZ1/QIAcube/QIAsymph"""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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              9237155V-Housing with Sample NeedleCNY


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