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Inosine Fluorometric Assay Kit

点击次数:17发布时间:2016/7/28 20:30:55

Inosine Fluorometric Assay Kit

更新日期:2016/7/28 20:30:55

所 在 地:中国大陆

产品型号:

简单介绍:Inosine Fluorometric Assay Kit 货号K712-100 100 assays 美国 Biovision进口,齐一生物代理,部分产品现货供应 齐一生物科技(上海)有限公司销售:021-6034 8496;181214 53965;173021 04490

相关标签:Inosine Fluorometric Assay Kit 

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 Inosine Fluorometric Assay Kit齐一生物长期出售上万种进口试剂.对照品.药物杂质.中检所对照品.Sigma西格玛.美国BD.赛默飞thermofisher.日本wako.TCL.默克Merck .美国AMRESCO.Invitrogen.日本荣研化学株式会社.EP(欧洲药典).USP(美国药典).BP(英国药典).加拿大TRC.美国CaTO.标准品.对照品等保证原装产品,原装质量.到货快捷安全,专业的物流配送,专人全程跟踪订单,确保货物安全.准确.及时地送达指定地点.欢迎咨询。齐一生物销售:0216034 8496181214 53965173021 04490

 

Inosine Fluorometric Assay Kit齐一生科技(上海)有限公司感谢您的查阅与咨询!期待与您的真诚合作!

 

低价格现货供应,欢迎前来选购。齐一生物销售:0216034 8496181214 53965173021 04490网站:www.qiyibio.comInosine Fluorometric Assay Kit

9240634  Power Supply, Main PCB, Aztec, AP196/98         CNY                           

9240630  Power Supply, 5VDC 1.5 AMP, AP96          CNY                           

9240593  Unload Valve, Pump, Pressure, AP196/98            CNY                           

9240562  Fuse, PCB, 315, Eppendorf, AP196/98        CNY                           

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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

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Service response time (repair): 5 business days

Periodic inspection/maintenance: not included

Inspection/maintenance delivery: not applicable

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Cost coverage for labor: yes, full coverage

Cost coverage for travel: yes, full coverage

Replacement system (Loaner) provision: not applicable

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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.

 

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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