19076Buffer ATL200 ml Tissue Lysis Buffer for 1000 prepsCNY

19048EndoFree Plasmid Buffer SetBuffers P1, P2, P3, QBT, QC, QN, ER, TE, Endotoxin-free water, RNase A; for 10  plasmid mega- or 5 gigapreps (endotoxin-free)CNY

12961QIAGEN Plasmid Plus Maxi Sample Kit (5)QIAGEN Plasmid Plus Kits enable ultrafast, large-scale plasmid purification of pure plasmid DNA. The use of a vacuum manifold allows purification of up to 12 (Mega ａnd Giga) or up to 24 (Midi ａnd Maxi) samples in parallel with low hands-on needs. Low elution volumes yield highly concentrated plasmid DNA for direct use without ethanol precipitation. QIAGEN Plasmid Plus Kits also feature a novel wash buffer for endotoxin reduction.CNY

12243QIAfilter Plasmid Midi Kit (25)25 QIAGEN-tip 100, Reagents, Buffers, 25 QIAfilter Midi CartridgesCNY

12123QIAGEN Plasmid Mini Kit (25)25 QIAGEN-tip 20, Reagents, BuffersCNY

133276NeXtalStock Spermine (100)CNY

4503065artus CMV LC PCR Kit (96) CECNY

6000-5000Specimen Collection TubesCNY

5000-1430MST Vortexer II - FoamFeetAssembly, 110VCNY

5128-1220Specimen Transport Medium (STM) CECNY

5123-1220Female Swab Specimen Collection KitTMCNY

5100-1400IVDhc2 Sample Conversion KitCNY

EA11424EASYartus BKV RG_IICNY

5050-1075 V.1CD Rom Manual, MST Vortexer 2CNY

EA10124EASYartus EBV RG PCR Kit 2CNY

BR-02DxS B-RAF Mutation Test KitCNY

9240729Tubing, 3/8"OD , Red, APCNY

9240719Cable Carrier, Capper, Elevator, APCNY

9240701O-Ring, Shaker, Lower Body, AP96/196CNY

9240696Fitting, Barbed, 1/4" ID tube, APCNY

9243651Comprehen Valid., QIAgility"""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

218076miScript SYBR Green PCR Kit (2000)CNY

271906cattletype Milk Prep Kit (50)CNY

289980intype IC-DNA (1ml)CNY

280437virotype BTV RT-PCR Kit (480)CNY

932836#QIAsymphony Ni-NTA Denat. Kit (384)CNY

800511Verification Sequencing / DNA productionCNY

9238243ZLV BioRobot M96 User ManualCNY

9019988ZLV Mainboard, QGYCNY

9020553Foam angle, transport box, QIACCNY

9020582X-Motor, DML3000CNY