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苯甲基-2-磺酰三硝基三氮唑CAS:74257-00-4

点击次数:29发布时间:2016/8/29 23:03:05

苯甲基-2-磺酰三硝基三氮唑CAS:74257-00-4

更新日期:2018/4/2 11:32:30

所 在 地:中国大陆

产品型号:

简单介绍:苯甲基-2-磺酰三硝基三氮唑CAS:74257-00-4 英文名称:MSNT 规格:AR,99% 包装:5克 齐一生物科技(上海)有限公司销售:021-6034 8496;181214 53965;173021 04490

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 苯甲基-2-磺酰三硝基三氮唑CAS:74257004齐一生物销售:0216034 8496181214 53965173021 04490

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"苯甲基-2-磺酰三硝基三氮唑CAS:74257004   英文名称:MSNT   规格:AR99%   包装:5      熔点: 132134°C

比重: 1·51

储存条件: 28

用途: 合成寡核苷酸的试剂

介绍: 常温易分解。"

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9235538       Teaching Tool              CNY                          

9230282       Cable, RS323, robot to syringe pump, 225            CNY                          

5050-2002    hc2 Software V2 Package         CNY                          

BS96RNA    BioSprint 96 to RNA (384) - UDP          CNY                           【苯甲基-2-磺酰三硝基三氮唑CAS:74257004

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9240713       Poly Muffler Kit, AP96/196              CNY                          

9240690       Bearings, Lead Screws, AP              CNY                          

9243654       Comprehen 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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9013207       Service kit, accessories, BR8000             CNY                          

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9013187       Holder, retractable tubing, dispenser, B           CNY                          

800328  Miniprep, PCR purification (Easy-Read)         CNY                          

132109  EasyXtal 15-Well DG-Tool X-Seal (100)       "100 empty 15-well crystallization plates with dropguard, X-Seal crystallization supports

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QY-x1845     人乳腺癌     MCF7                               

QY-x1846     小鼠神经成纤维细胞瘤  N2a       Albino mouse                           

QY-x1847     小鼠神经成纤维细胞瘤GFP N2a-GFP                                 

QY-x1848     人大肺细胞癌细胞   NCIH460                                

QY-x1849     NIH小鼠成纤维细胞      NIH 3T3                                  

QY-x1850     人卵巢癌细胞    OVCaR-3                                

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QY-x1852     猪卵母细胞 PFF                                  

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QY-x1855     Bac-to-Bac杆状病毒载体表达系统    SF9                            

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QY-x1858     人卵巢癌     SKOV3                             【苯甲基-2-磺酰三硝基三氮唑CAS:74257004

QY-x1859            SP-210                             

QY-x1860     人脑胶质母细胞瘤细胞  SW038-C2                              

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QY-x1872     L-02 人肝细胞                                          

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QY-x1874     LA795 肺腺癌 瘤株 S180 腹水瘤 瘤株                                          【苯甲基-2-磺酰三硝基三氮唑CAS:74257004

QY-x1875     H22 肝癌 瘤株 B16 黑色素瘤 体外培养株                                           

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