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hCEA-ELISA

點擊次數(shù):9發(fā)布時間:2016/6/16 0:01:02

hCEA-ELISA

更新日期:2016/6/16 0:01:02

所 在 地:中國大陸

產(chǎn)品型號:

簡單介紹:EK0904 hCEA-ELISA 人CEAELISA試劑盒 Human CEA ELISA Kit 96 tests

相關(guān)標(biāo)簽:hCEA-ELISA 

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詳細(xì)內(nèi)容

 hCEA-ELISA齊一生物專業(yè)經(jīng)營銷售通用試劑.分析試劑.標(biāo)準(zhǔn)物質(zhì).合成試劑.中間體.催化劑.生化試劑等化學(xué)產(chǎn)品,我們致力于以專業(yè)化的視角,提供豐富專業(yè)產(chǎn)品資料及其相關(guān)技術(shù)開發(fā)資訊,產(chǎn)品內(nèi)容覆蓋分析化學(xué).無機化學(xué).有機化學(xué).生命科學(xué).材料科學(xué)等領(lǐng)域. hCEA-ELISA已迅速發(fā)展成為國內(nèi)科學(xué)試劑的運營商,是國家重點實驗室指定供應(yīng)商,并與國內(nèi)多家科研單位緊密合作. 齊一生物銷售:0216034 8496;181214 53965173021 04490網(wǎng)站:http://www.qiyibio.com

 

hCEA-ELISA齊一生物科技(上海)有限公司經(jīng)營試劑種類眾多:覆蓋分析化學(xué)品,無機化學(xué)品,有機化學(xué)品,生物化學(xué)品,材料化學(xué)品等.試劑信息齊全:包含試劑特性描述,詳細(xì)質(zhì)量信息,應(yīng)用方法.標(biāo)準(zhǔn)科研 用途以及正在開發(fā)的前沿應(yīng)用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

 

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QY-07430CTGF (connective tissue growth factor)結(jié)締組織生長因子(多肽抗原) 0.5mg/6501mg/1100

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QY-03990Deltex-1(DTX1) (Deltex protein 1)抗原 0.5mg/6501mg/1100

QY-04280DISC1(disrupted in schizophrenia1)(NT)DISC1 N端抗原 0.5mg/6501mg/1100

QY-04300DISC1(disrupted in schizophrenia1)(CT)DISC1 C端抗原 0.5mg/6501mg/1100

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QY-07140E7 protein/HPV 16 (Human papillomavirus type 16)人乳頭瘤病毒16型E7蛋白抗原 0.5mg/6501mg/1100

QY-01650EGF-R (Epidemal growth factor receptor)表皮生長因子受體(抗原) 0.5mg/6501mg/1100

 

QY-01650EGF-R (Epidemal growth factor receptor)表皮生長因子受體(抗原) 0.5mg/6501mg/1100


9240730Tubing, 1/4" OD, Red, APCNY
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9243654Comprehen Valid., Other Quant. 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).   For planning purposes and to ensure a smooth process, the Customer is expected to have all materials on-hand and inventoried one (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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Taq DNA Polymerase is supplied with CoralLoad PCR Buffer, which has all of the advantages of QIAGEN PCR Buffer but can also be used to directly load the PCR reaction onto an agarose gel without the need to add a gel loading buffer. CoralLoad PCR Buffer provides the same high PCR specificity and minimal reaction optimization as conventional QIAGEN PCR Buffer. Additionally, it contains two marker dyes: an orange dye and a red dye, that facilitate estimation of DNA migration distance and optimization of agarose gel run time."CNY
 

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