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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 >  创伤弧菌荧光定量PCR检测试剂盒

创伤弧菌荧光定量PCR检测试剂盒

创伤弧菌荧光定量PCR检测试剂盒

  • 价 格: 电议
  • 型号:
  • 生 产 地:中国大陆
  • 访问:23次
  • 发布日期:2016/6/20(更新日期:2016/6/20)

齐一生物科技(上海)有限公司

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QYD657 创伤弧菌荧光定量PCR检测试剂盒 48次/盒
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  • 公司简介
 创伤弧菌荧光定量PCR检测试剂盒齐一生物专业代理Sigma西格玛.美国BD.赛默飞.日本wako.TCL.默克Merck .美国AMRESCO.日本荣研化学株式会社.EP(欧洲药典).USP(美国药典).BP(英国药典)加拿大TRC等试剂.标准品.对照品齐一生物销售:0216034 8496181214 53965173021 04490网站:www.qiyibio.com

 

创伤弧菌荧光定量PCR检测试剂盒齐一生物专业代理Sigma西格玛.美国BD.赛默飞thermofisher.日本wako.TCL.默克Merck .美国AMRESCO.Invitrogen.日本荣研化学株式会社.EP(欧洲药典).USP(美国药典).BP(英国药典)加拿大TRC等试剂.标准品.对照品原装产品,正品原装质量,货期短价格优惠!欢迎前来选购齐一生物销售:0216034 8496181214 53965173021 04490网站:http://www.qiyibio.com创伤弧菌荧光定量PCR检测试剂盒

 

9238479Motor, syringe, RapidPlateCNY

9238152Elution Microplate Adapter 8000, SBSCNY

9237932Syringe, 100µlCNY

9240663Nut, Flangeless,1/4-28, Black, APCNY

9240634Power Supply, Main PCB, Aztec, AP196/98CNY

9240630Power Supply, 5VDC 1.5 AMP, AP96CNY

9240593Unload Valve, Pump, Pressure, AP196/98CNY

9240562Fuse, PCB, 315, Eppendorf, AP196/98CNY

9240536Motor Assy, SiNug, 17, All, AP96/196CNY

9240514CD R/W, AP196/98CNY

9240504PC-104, AP98CNY

9240346Autopure, Full Agreement"Repair service delivery: onsite

Service response time (repair): 48 hours/2 business days

Periodic inspection/maintenance: yes, 1/agreement year

Inspection/maintenance delivery: onsite

Cost coverage for repair parts: yes, included

Cost coverage for labor: yes, included

Cost coverage for travel: yes, included

Replacement system (Loaner) provision: not included

Transportation cost coverage: not applicable"CNY

9240098Re-Installation, BR EZ1The Re-Installation, BR EZ1 facilitates quick implementation of system back into lab routine by minimizing  instrument set-up phase. It covers hardware and software check of instrument and provides user with operator refesher overview.  Re-installation includes labor and travel costs. Re-installation performance process is documented on a GMP/GLP-compliant Field Service document.CNY

9239852Foot bumpers,  v2.0 (4)CNY

9019944Cable, P-axis, wires, 8 ch. , C18CNY

9238880Bearings up. & low, BS96CNY

9238836BioSprint96, Basic Agreement, no PM"Repair service delivery: onsite

Service response time (repair): 5 business days

Periodic inspection/maintenance: not included

Inspection/maintenance delivery: not applicable

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: not applicable"CNY

9241211Full Agreement Depot Repair, DML2000, 1y"The Full Agreement Depot Repair, DML2000 provides full service coverage for the DML 2000 luminometer. The service is conducted as an instrument exchange service. 

All shipping, labor and repair part costs related to an instrument exchange are included for 1 year. Instrument exchange time is 2 - 3 working days."CNY

9241191Magnet, tool, QXCNY

9238825Spare bucket for plate rotorCNY

9238815Rect. carrier for 12 tubes 10 ml w/ capCNY

9019472TAPE SPACER CLEAR GSCNY

9019464UV tube, CxxCNY

9243650Comprehen Valid., EZ1/QIAcube/QIAsymph"""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).   The Customer is expected to have all materials on-hand 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

9237333Install, BR plus 3 integr. w. schedulingInstallation and training, BioRobot System including three approved integration devices with schedulingCNY

9237328Upgrade, BR & 2 ext. devices w. sched.Upgrade BioRobot with two approved integration devices using scheduling softwareCNY

9237173Shield, V-housingCNY

9233208Tubing, liquid system 2.5/1.5CNY

9237155V-Housing with Sample NeedleCNY

 

9237150Heater TopCNY


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科研之路。您我并肩同行!齐一生物科技(上海)有限公司具有完善的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。齐一生物科技(上海)有限公司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.齐一生物科技(上海)有限公司全国热线:400-991-0197电话: 手机:18121453965王经理
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