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您的位置:首页 > 产品展厅 >  化工原料 >  化学试剂 >  生化试剂 >  克伦特罗检测试剂盒(96孔)

克伦特罗检测试剂盒(96孔)

克伦特罗检测试剂盒(96孔)

  • 价 格: 电议
  • 型号:
  • 生 产 地:中国大陆
  • 访问:26次
  • 发布日期:2016/6/21(更新日期:2016/8/27)

齐一生物科技(上海)有限公司

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QTR-1167 克伦特罗检测试剂盒(96孔)
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  • 公司简介
 克伦特罗检测试剂盒(96)齐一生物科技(上海)有限公司检测试剂盒产品已被广泛应用于化学.化工.生命科学的基础研究和开发应用.制药.疾病诊断与控制.人口与健康.生物技术等诸多领域. 克伦特罗检测试剂盒(96)客户遍布国内各大学.研究所.医院.卫生防疫.商品检验检疫.制药公司.生物技术公司和食品工业等单位. 齐一生物销售:0216034 8496181214 53965173021 04490网址:www.qiyibio.com

 

克伦特罗检测试剂盒(96)是我公司重点推广产品,我公司有专业的人员进行全程指导,请放心购买,发货时均会附上质检报告单.使用说明书和推荐用法用量,提供正规发票. 齐一生物销售:0216034 8496181214 53965173021 04490网址:www.qiyibio.com

 

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

270803cattletype MAP Ab (5)CNY

 

280303cador BVDV RT-PCR Kit (24)CNY


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QT-00252多粘类芽孢杆菌CMCC63512冻干粉
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QT-00257蜡状芽孢杆菌CMCC63302冻干粉
QT-00258多黏类芽孢杆菌CMCC63512冻干粉
QT-00259大肠埃希氏菌(大肠杆菌)CMCC44108冻干粉
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QT-00269福氏志贺氏菌CMCC(B)26003冻干粉
QT-00270痢疾志贺氏菌CMCC(B)51252冻干粉
QT-00271福氏志贺氏菌CMCC(B)51572冻干粉
QT-00272宋氏志贺氏菌CMCC(B)51592冻干粉
QT-00273阴沟肠杆菌CMCC(B)45301冻干粉
QT-00274肠埃希氏菌CMCC(B)44103冻干粉
QT-00275单核增生性李斯特氏菌CMCC(B)54002冻干粉
QT-00276已型副伤寒沙门氏菌CMCC(B)50094冻干粉
QT-00277枯草芽孢杆菌CMCC(B)63501冻干粉
QT-00278小肠结肠炎耶尔森氏菌CMCC(B)52204冻干粉
QT-00279粘质沙雷伯氏菌CMCC(B)41002冻干粉
 

科研之路,您我并肩同行!齐一生物具有完善的ELISA试剂盒开发平台,成熟的抗原、抗体研发系统,熟练掌握各种酶联技术,如双抗夹心法、(直接)竞争法、间接竞争法、阻断法、间接法、双抗原夹心法等方法,结合我公司的诊断试剂开发团队我们可以有效的将试剂盒开发为临床诊断级别,质量处于全国前茅。齐一生物针对中高端客户推出自主品牌QIYBO试剂盒为了保证客户用货质量,我公司采用纯进口原料现包被生产,质量稳定高.
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