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吸水鏈霉菌紫色變種ACCC40034

點擊次數(shù):16發(fā)布時間:2016/7/18 21:47:26

吸水鏈霉菌紫色變種ACCC40034

更新日期:2016/7/18 21:47:26

所 在 地:中國大陸

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簡單介紹:吸水鏈霉菌紫色變種ACCC40034 貨號:QT-00394 凍干粉 齊一生物科技(上海)有限公司銷售:021-6034 8496;181214 53965;173021 04490

相關(guān)標(biāo)簽:吸水鏈霉菌紫色變種ACCC40034 

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 吸水鏈霉菌紫色變種ACCC40034齊一生物專業(yè)代理Sigma西格瑪.美國BD.賽默飛.日本wako.TCL.默克Merck .美國AMRESCO.日本榮研化學(xué)株式會社.EP(歐洲藥典).USP(美國藥典).BP(英國藥典)加拿大TRC等試劑.標(biāo)準(zhǔn)品.對照品齊一生物銷售:0216034 8496181214 53965;173021 04490網(wǎng)站:www.qiyibio.com

 

吸水鏈霉菌紫色變種ACCC40034齊一生物專業(yè)代理Sigma西格瑪.美國BD.賽默飛thermofisher.日本wako.TCL.默克Merck .美國AMRESCO.Invitrogen.日本榮研化學(xué)株式會社.EP(歐洲藥典).USP(美國藥典).BP(英國藥典)加拿大TRC等試劑.標(biāo)準(zhǔn)品.對照品原裝產(chǎn)品,正品原裝質(zhì)量,貨期短價格優(yōu)惠!歡迎前來選購齊一生物銷售:0216034 8496;181214 53965;173021 04490網(wǎng)站:http://www.qiyibio.com吸水鏈霉菌紫色變種ACCC40034

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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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9013401  Cable set, cooling system, 90/120        CNY                           

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QY-x172  HT-29結(jié)腸癌細(xì)胞        HTB-38                              

QY-x173  KG-1白血病細(xì)胞  CCL-246                                   

QY-x174  LoVo結(jié)腸癌細(xì)胞   CCL-229                                   

QY-x175  THP-1單核細(xì)胞白血病       TIB-202                             

QY-x176  SW620結(jié)腸癌細(xì)胞      CCL-227                                   

QY-x177  SK-N-SH神經(jīng)母細(xì)胞瘤細(xì)胞       HTB-11                              

QY-x178  SH-SY5Y神經(jīng)母細(xì)胞瘤細(xì)胞       CRL-2266                                 

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