微囊藻毒素/节球藻毒素(ADDA)检测试剂盒

【微囊藻毒素/节球藻毒素(ADDA)检测试剂盒】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。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。【微囊藻毒素/节球藻毒素(ADDA)检测试剂盒】齐一生物销售：021－6034 8496；181214 53965；173021 04490网址：www.qiyibio.com

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

9016151#App. Package, M48, PathologyCNY

9019179Opto - plate lock closed, PyroQ96MDCNY

9011883Upgrade, high speed pipetting systemCNY

9011882Back unit, BR9600CNY

9011823Z-Modul; Tip-Adapter 300µl; BR8000CNY

92369163 Year Warranty, LiquiChipLiquiChip 3-year Warranty with 1 Preventive Maintenance per year.  Included in system price.  This warranty must be included as a line item on the system quote.  It covers the system for three years total including all per incident travel ａnd labor charges, all repair parts, one preventive maintenance visits per year (three in total), ａnd 48- hour priority response.CNY

9019143Power supply, PyroQ96CNY

9019129Cable - Reagent, PyroQ96IDCNY

9019126PCB 2 - Connection, PyroQ96IDCNY

9019114IPC mainboard, PyroQ96IDCNY

9019025Worktable, side wall, left, EZ1xlCNY

9019012Motor Y, EZ1xlCNY

9018942Adapter, 2xRing of 12 COBAS AmplicoreCNY

9022737Rotor-Gene AssayManager SOWCNY

9016061Tubing Set, Syringe inlet, BR8000 ICNY

9015823CD, Field Syringe Calibration, BR8000CNY

9015690Rings (10), pinching, 4.5/3.2 mmCNY