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anti-DYKDDDDK Tag (NT)/Flag-Tag polyclonal antibody抗標(biāo)簽DYKDDD
點(diǎn)擊次數(shù):11發(fā)布時間:2016/7/20 17:27:12

更新日期:2016/7/20 17:27:12
所 在 地:中國大陸
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【anti-DYKDDDDK Tag (NT)/Flag-Tag polyclonal antibody抗標(biāo)簽DYKDDDDK Tag抗體(N端)】齊一生科技(上海)有限公司感謝您的查閱與咨詢!期待與您的真誠合作!
低價格現(xiàn)貨供應(yīng),歡迎前來選購。齊一生物銷售:021-6034 8496;181214 53965;173021 04490網(wǎng)站:www.qiyibio.com【anti-DYKDDDDK Tag (NT)/Flag-Tag polyclonal antibody抗標(biāo)簽DYKDDDDK Tag抗體(N端)】
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5000-1404 Plate Cartridge 110V, VTX2 CNY
5000-1277 Top Housing W LID, DML2 CNY
5050-1029 Mouse, PC System spare CNY
5025-1011 Expand 4 Pipettor 240V CNY
9240747 Belt, Reagent Pump 117 groove, AP CNY anti-DYKDDDDK Tag (NT)/Flag-Tag polyclonal antibody抗標(biāo)簽DYKDDDDK Tag抗體(N端)
9240720 Cable Carrier, Tubing, Dispense Head, AP CNY
9240700 Tubing, Waste, 1 1\4", AP CNY
9243690 DML Luminometer, Repair Fee DML Repair Fee covers Regional Repair Center service for non-service agreement covered DML 2000 and DML 3000 units. Includes labor, parts and shipping materials. CNY
9243652 Comprehen Valid., QuantiPlex/QP Hyres """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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280303 cador BVDV RT-PCR Kit (24) CNY
282303 virotype PRRSV RT-PCR Kit (24) CNY
282305 virotype PRRSV RT-PCR Kit (96) CNY
280443 virotype BTV pan/8 RT-PCR Kit (24) CNY
939012 Buffer N2 (2 x 10 ml) CNY
871105 EGFR PCR Kit (100) CNY
800382 Restriction Map CNY
871005 KRAS PCR Kit (100) CNY
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