【梔子苷24512-63-8】齊一生物科技（上海）有限公司經(jīng)營試劑種類眾多：覆蓋分析化學(xué)品,無機(jī)化學(xué)品,有機(jī)化學(xué)品,生物化學(xué)品,材料化學(xué)品等.試劑信息齊全：包含試劑特性描述,詳細(xì)質(zhì)量信息,應(yīng)用方法.標(biāo)準(zhǔn), 科研 用途以及正在開發(fā)的前沿應(yīng)用歡迎前來選購齊一生物銷售：021－6034 8496；181214 53965；173021 04490網(wǎng)站：http://www.qiyibio.com

9238854#BR M96, Basic AgreementThe Basic Cover Agreement M96 provides full service coverage for the BioRobot M96. Costs for service visits are fully covered including travel, labor, ａnd parts. The agreement also includes one annual preventive maintenance visit, with costs for labor ａnd parts covered. With a Basic Cover Agreement, the response time is 5 working days.CNY

9238842RS232 box, non-online fill, RapidPlateCNY

9241215Full Agreement Depot Repair, Shaker, 1yr"The Full Agreement Depot Repair, Shaker provides full service coverage for the plate shaker used in the digene HPV application. 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

9238833#BR 9604, Basic AgreementThe Basic Cover Agreement 9604, 1 PM provides full service coverage for the BioRobot 9604. Costs for service visits are fully covered including travel, labor, ａnd parts. The agreement also includes one annual preventive maintenance visit, with costs for labor ａnd parts covered. With a Basic Cover Agreement, the response time is 5 working days.CNY

9238832BR 9600, Basic AgreementThe Basic Cover Agreement 9600 provides full service coverage for the BioRobot 9600. Costs for service visits are fully covered including travel, labor, ａnd parts. The agreement also includes one annual preventive maintenance visit, with costs for labor ａnd parts covered. With a Basic Cover Agreement, the response time is 5 working days.CNY

9238819Rect. carrier for 5 glass tubes 25mlCNY

9237527Software LiquiChip Workstation IS V2.2.CNY

9237380Installation, BR MDx & 2 react. setupInstallation ａnd training, including two customized reaction setup protocolsCNY

9237379Installation, BR MDx & 1 react. setupInstallation ａnd training, including one customized reaction setup protocolCNY

9237378BR MDx, InstallationThe Installation, BR MDx facilitates the quick implementation of the BioRobot MDx into the lab routine by minimizing the instrument start-up phase. It covers the hardware ａnd software installation of the BioRobot MDx instrument ａnd provides the user with an introductory training on operation ａnd user maintenance. The installation includes labor ａnd travel costs. The performance of the installation process is documented on a GMP/GLP-compliant Field Service document.CNY

9237175Guard Fan, Platic XYPCNY

9233209Tubing, 3/2,CNY

9233155Power Cord, EuropeanCNY

9236418Board, CPU, TWICNY

9236345Red LSRCNY

9236166Safety shield, RapidPlateCNY

9230863Anpressplatte Rose-80CNY

9235538Teaching ToolCNY

9230282Cable, RS323, robot to syringe pump, 225CNY

5050-2002hc2 Software V2 PackageCNY

BS96RNABioSprint 96 to RNA (384) - UDPCNY

9240730Tubing, 1/4" OD, Red, APCNY

9240713Poly Muffler Kit, AP96/196CNY

9240690Bearings, Lead Screws, APCNY

9243654Comprehen Valid., Other Quant. Sys."""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

6000-5013LumiCheck Plate User PackageCNY

288103bactotype Mycoplasma Mg/Ms PCR Kit (24)CNY

1048147QIAamp Viral RNA Mini Accessory SetCNY

270043cattletype BHV1 gB Ab (5)CNY

1019992Buffer Set (RNeasy 96 BioRobot 9604 KitCNY

273401pigtype Toxoplasma Ab (1)CNY