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Inosine Fluorometric Assay Kit

點(diǎn)擊次數(shù):17發(fā)布時(shí)間:2016/7/28 20:30:55

Inosine Fluorometric Assay Kit

更新日期:2016/7/28 20:30:55

所 在 地:中國(guó)大陸

產(chǎn)品型號(hào):

簡(jiǎn)單介紹:Inosine Fluorometric Assay Kit 貨號(hào)K712-100 100 assays 美國(guó) Biovision進(jìn)口,齊一生物代理,部分產(chǎn)品現(xiàn)貨供應(yīng) 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:Inosine Fluorometric Assay Kit 

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詳細(xì)內(nèi)容

 Inosine Fluorometric Assay Kit齊一生物長(zhǎng)期出售上萬(wàn)種進(jìn)口試劑.對(duì)照品.藥物雜質(zhì).中檢所對(duì)照品.Sigma西格瑪.美國(guó)BD.賽默飛thermofisher.日本wako.TCL.默克Merck .美國(guó)AMRESCO.Invitrogen.日本榮研化學(xué)株式會(huì)社.EP(歐洲藥典).USP(美國(guó)藥典).BP(英國(guó)藥典).加拿大TRC.美國(guó)CaTO.標(biāo)準(zhǔn)品.對(duì)照品等保證原裝產(chǎn)品,原裝質(zhì)量.到貨快捷安全,專業(yè)的物流配送,專人全程跟蹤訂單,確保貨物安全.準(zhǔn)確.及時(shí)地送達(dá)指定地點(diǎn).歡迎咨詢。齊一生物銷售:0216034 8496181214 53965;173021 04490

 

Inosine Fluorometric Assay Kit齊一生科技(上海)有限公司感謝您的查閱與咨詢!期待與您的真誠(chéng)合作!

 

低價(jià)格現(xiàn)貨供應(yīng),歡迎前來(lái)選購(gòu)。齊一生物銷售:0216034 8496181214 53965;173021 04490網(wǎng)站:www.qiyibio.comInosine Fluorometric Assay Kit

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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

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Cost coverage for Repair Parts : yes, full coverage

Cost coverage for labor: yes, full coverage

Cost coverage for travel: yes, full coverage

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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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QY-x923  人食管鱗癌KYSE70                                       

QY-x924  人食管癌細(xì)胞KYSR450                                        

QY-x925  人食管癌細(xì)胞KYSE510                                         

QY-x926  人胃癌細(xì)胞系HS-746T                                         

QY-x927  人胃癌細(xì)胞BSG823                                       

QY-x928  人胃粘膜細(xì)胞GES-1                                      

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QY-x930  人胃腺癌細(xì)胞MCG803                                         

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QY-x932  人低分化胃癌細(xì)胞SGC7901                                         

QY-x933  人耐VCR胃腺癌細(xì)胞SGC-7901/VCR                                         

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QY-x935  人未分化胃癌細(xì)胞HGC-27                                     Inosine Fluorometric Assay Kit

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