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溫和氣單胞菌核酸檢測試劑盒熒光法

點擊次數:11發(fā)布時間:2016/6/14 21:20:35

溫和氣單胞菌核酸檢測試劑盒熒光法

更新日期:2016/6/14 21:20:35

所 在 地:中國大陸

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簡單介紹:QKT0857 溫和氣單胞菌核酸檢測試劑盒熒光法

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 溫和氣單胞菌核酸檢測試劑盒熒光法齊一生物長期經營ELISA試劑盒及抗體(免費代測)、分子學生物試劑盒、比色法,IFCC推薦法,化學氧化法,速率法等檢測試劑盒、細胞菌株、培養(yǎng)基、細胞因子、生化試劑、耗材等生物試劑產品。誠信經營,價格實惠,服務周到,質量保障!提供各種實驗代測服務。歡迎新老客戶來電咨詢!

溫和氣單胞菌核酸檢測試劑盒熒光法齊一生物科技(上海)有限公司專業(yè)經營高效液相色譜法、可見分光光度法、紫外分光光度法、酶標法檢測試劑盒齊一生物銷售:0216034 8496;181214 53965;173021 04490溫和氣單胞菌核酸檢測試劑盒熒光法

 

QYD862檢砷管速測盒30次/袋

QYD863檢汞管速測盒30次/袋

QYD864肉制品色素速測盒50次/袋

QYD865豆?jié){生熟度的檢測80次/袋

QYD866雞蛋新鮮度速測劑200ml/袋

QYD867食用油中桐油速測鑒別試劑50次/袋

QYD868食用油中大麻油速測鑒別試劑10次/袋

QYD869食用油中巴豆油速測鑒別試劑10次/袋

QYD870食用油中礦物油速測鑒別試劑10次/袋

QYD871蜂蜜酸度速測液25次/袋

QYD872蜂蜜中飴糖速測液100次/袋

QYD873蜂蜜比重計(水分測定)比重計

QYD874蜂蜜中蔗糖含量速測液(定性)100次/袋

QYD875蜂蜜中蔗糖含量速測液(半定量)

QYD876蜂蜜中果糖、葡萄糖速測液100次/袋

QYD877液態(tài)奶中摻加甲醛的檢測試劑100次/袋

QYD878液態(tài)奶中摻加豆?jié){的檢測試劑100次/袋

QYD879液態(tài)奶中摻加淀粉的檢測試劑60次/袋

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QYD881液態(tài)奶中摻加尿素的檢測試劑50次/袋

QYD882液態(tài)奶中摻加食鹽的檢測試劑50次/袋

QYD883液態(tài)奶中摻加碳酸鈉的檢測試劑50次/袋

QYD884液態(tài)奶中摻加亞硝酸鹽的檢測試劑100次/袋

QYD885液態(tài)奶中摻加銨鹽的檢測試劑50次/袋

QYD886乳稠計(奶純度)乳稠計

QYD887碘鹽含量速測液200次/袋

QYD888游離性余氯速測盒200次/袋

QYD889水解蛋白快速檢測試劑盒50次/袋

QYD890原料乳中硫氰酸鈉摻假定性檢測20次/袋

QYD891β-內酰胺酶高通量快速檢測試劑盒20次/袋

 

QYD892組織樣品沙丁胺醇快速檢測試劑盒20次/袋


9240977Tray, sample tracking, QsymCNY
9240966Sensor, z, pipetting system, QsymCNY
9240686Autodrain, Kit, Water Trap, AP196/98CNY
9240681Dump Tray, Overflow Control, AP96/196CNY
9240787Update, Capper In/Out Motor, AP98CNY
6000-5013RLumiCheckPlate User Package(Refurbished)CNY
9241783Rotor - Gene Q Demopool BoxCNY
9241769QIAxtractor, Full AgreementThe Full Agreement, QIAxtractor provides full service coverage for the QIAxtractor and the CAS 1280. Costs for service visits are fully covered including travel, labor, and parts. One on-site pipetting head service and inspection is included . With a Full Agreement, there is a priority response time of 48 hours (2 working days).CNY
9241368Interlock, IL1, EZ1aCNY
9241366Cable, UV lamp voltage converter, EZ1aCNY
9240762Co-Processor, AP96CNY
9240760Update, Bucket/Elevator Head, AP196/98CNY
9243549Pyro Q96 MD, PM Service"Service response time (repair): not applicable
Periodic inspection/maintenance: yes
Inspection/maintenance delivery: onsite
Cost coverage for Repair Parts : not included
Cost coverage for labor: yes, full coverage
Cost coverage for travel: yes, full coverage
Replacement system (Loaner) provision: not applicable
Transportation cost coverage: yes, full coverage"CNY
9242786RCS, Full Agreement, 2PM"Repair service delivery: onsite and to Regional Repair Center
Service response time (repair): 48 hours/2 business days or 7-10 working days for RRC repairs
Periodic inspection/maintenance: yes, 2/agreement year
Inspection/maintenance delivery: onsite for RCS only
Cost coverage for Repair Parts : yes, full coverage
Cost coverage for labor: yes, full coverage
Cost coverage for travel: yes, full coverage
Replacement system (Loaner) provision: not applicable
Transportation cost coverage: yes, included"CNY
9242714Validation Support, 5d, QIAgilityThe QIAGEN QIAgility Accelerated Validation Support service includes all travel and labor charges for a site visit up to 5 days by a QIAGEN Specialist.  A QIAGEN specialist will provide an introduction to the QIAgility system and software, review the User Manual, as well as hands-on user support and QIAgility instrument operation.  The Accelerated Validation service includes guidance on the laboratory’s validation experimental design, internal validation documentation support, and QIAGEN sponsored data templates. The QIAGEN Specialist will support the customer by running samples through the QIAGEN-only extraction method/system (does not include phenol-chloroform or similar methods), as well as general wet lab support such as pipetting for quantification, STR and CE setup, normalization, etc. to produce the data needed for the validation study. The customer is responsible for submitting the data to QIAGEN for assisted data analysis. The customer is responsible for final documentation and report using QIAGEN prepared templates provided with the final product. Enough consumable chemistry and accessories (QIAGEN or other vendors) should be purchased to cover the validation experimental design and are not included in the cost of validation support.  Please indicate which processes (quant setup, normalization, PCR setup, CE setup) and kit manufacturer (Applied Biosystems, Promega, QIAGEN) need to be included in the validation.CNY
9242531QIAsymphony SPAS, PM AgreementCNY
9242546Probe Holder Assembly, LX200, LCCNY
9242152Upgrade, CAS1820 vacuum DX/VX"The Upgrade, CAS 1820 vacuum DX/VX upgrades the X-tractorgene to use the improved vacuum system for the QIAxtractor. The upgrade is conducted as an on-site service, performed by a QIAGEN service specialist.
The upgrade allows for the usage of the QIAGEN DX and VX capture plates and the disposable silicon mats.
During the service, the new vacuum system is installed and the software is updated. Please note that due to the software upgrade the instrument will only run the QIAxtractor software applications. Customized run files from the previous version will have to be adapted beforehand for additional fees."CNY
5000-1404Plate Cartridge 110V, VTX2CNY
5000-1277Top Housing W LID, DML2CNY
5050-1029Mouse, PC System spareCNY
5025-1011Expand 4 Pipettor 240VCNY
9240747Belt, Reagent Pump 117 groove, APCNY
9240720Cable Carrier, Tubing, Dispense Head, APCNY
9240700Tubing, Waste, 1 1\4", APCNY
9243690DML Luminometer, Repair FeeDML 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
9243652Comprehen 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
6000-3101Rapid Capture SystemCNY
19134QIAGEN Proteinase KCNY
614033careHPV Test, SFDA (24-test)CNY
274203flocktype IBDV Ab (5)CNY
 

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