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Anti-ILK-1 (Integrin-linked protein kinase 1)整合素連接激酶-1抗體

點擊次數(shù):18發(fā)布時間:2016/7/21 20:57:43

Anti-ILK-1 (Integrin-linked protein kinase 1)整合素連接激酶-1抗體

更新日期:2016/7/21 20:57:43

所 在 地:中國大陸

產(chǎn)品型號:

簡單介紹:Anti-ILK-1 (Integrin-linked protein kinase 1)整合素連接激酶-1抗體 貨號:QY-14872 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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 Anti-ILK-1 (Integrin-linked protein kinase 1)整合素連接-1抗體齊一生物科技(上海)有限公司檢測試劑盒產(chǎn)品已被廣泛應用于化學.化工.生命科學的基礎研究和開發(fā)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(nèi)各大學.研究所.醫(yī)院.衛(wèi)生防疫.商品檢驗檢疫.制藥公司. 生物技術公司和食品工業(yè)等單位. Anti-ILK-1 (Integrin-linked protein kinase 1)整合素連接-1抗體齊一生物銷售:0216034 8496181214 53965;173021 04490網(wǎng)址:www.qiyibio.com

Anti-ILK-1 (Integrin-linked protein kinase 1)整合素連接-1抗體是我公司重點推廣產(chǎn)品,我公司有專業(yè)的人員進行全程指導,請放心購買,發(fā)貨時均會附上質(zhì)檢報告單.使用說明書和推薦用法用量,提供正規(guī)發(fā)票. 齊一生物銷售:0216034 8496;181214 53965173021 04490網(wǎng)址:www.qiyibio.com

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RND99012     呋喃它酮檢測試劑盒    Furaltadone (AMOZ) ELISA Test Kit    96T 美國REAGEN                     Anti-ILK-1 (Integrin-linked protein kinase 1)整合素連接激酶-1抗體】

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RND99029     氟苯尼考檢測試劑盒    Florfenicol ELISA Test Kit     96T 美國REAGEN                     Anti-ILK-1 (Integrin-linked protein kinase 1)整合素連接激酶-1抗體】

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931036    QIAsymphony Virus/Bact Mini Kit (192)             CNY                            Anti-ILK-1 (Integrin-linked protein kinase 1)整合素連接激酶-1抗體】

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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.

 

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