74121RNeasy Protect Starter KitRNAlater RNA Stabilization Reagent (20 ml), 6 RNeasy Mini Spin Columns, 2 RNeasy Midi Spin Columns, Collection Tubes (1.5 ａnd 2 ml), RNase-free Reagents ａnd BuffersCNY
74104RNeasy Mini Kit (50)50 RNeasy Mini Spin Columns, Collection Tubes (1.5 ml ａnd 2 ml), RNase-free Reagents ａnd BuffersCNY
72251TurboCapture 96 mRNA Kit (5)For rapid ａnd easy mRNA purification in high-throughput applications. The kit provides a fast ａnd simple procedure for purifying mRNA. Up to 96 samples can be processed simultaneously - ideal for high-throughput applications such as compound screening ａnd target validation (e.g. by siRNA screening).CNY
19407VacConnectors (500)500 disposable connectors for use with QIAamp spin columns on luer connectors. Should be ordered in conjuntion with 19408 - VacValves (24).CNY
12281QIAfilter Plasmid Mega Kit (5)5 QIAGEN-tip 2500, Reagents, Buffers, 5 QIAfilter Mega-Giga CartridgesCNY
12191QIAGEN Plasmid Giga Kit (5)5 QIAGEN-tip 10000, Reagents, BuffersCNY
4502103artus VZV TM PCR Kit (24) RUOCNY
133271NeXtalStock PIPES pH 7.0 (200)CNY
133270NeXtalStock Phosphate-citr. pH 5.2 (200)CNY
990512Filter-Tips, 50 µl (960)CNY
337620qBiomarker SYBR Green Fluor Mastermix(2)CNY
337011qBiomarker Somatic Mutations PCR AssaysCNY
4500263artus HSV-1/2 RG PCR Kit (24) CECNY
939016Buffer ATL ( 4 x 50 ml),GPRCNY
4500163artus HSV-1/2 TM PCR Kit (24) CECNY
1073925Ni-NTA Superflow (8 x 500 ml),cus,GCNY
9010931BGR Greifer P7 (alt)CNY
9010858BGR DT-Abstreifer 8-fach P7xxx DCNY
931036QIAsymphony Virus/Bact Mini Kit (192)CNY
133248NeXtalStock Sodium succinate pH6.5 (200)CNY
330603RT² SYBR Green FAST Mastermix (24)CNY
929608QX Pro Separation Buffer (40 ml)CNY
5000-1415Knob RB671CSKWL Matte, VTX2CNY
5000-1408Cable Shielded 1/17HP, VTX2CNY
L2170hc2 CT/GC HC2 DNA Test PI (CD-ROM)CNY
L1971Rotary Shaker User＇s ManualCNY
9240705O-ring Kit, Capper, Spindle, APCNY
9240693Actril Sterilant & Test Strips, APCNY
9243653Comprehen Valid., Other Extraction 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). 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
386516Investigator STR GO! Lysis Buffer (200)CNY
