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塑化劑檢測(cè)試劑盒
點(diǎn)擊次數(shù):62發(fā)布時(shí)間:2016/8/21 14:00:48

更新日期:2016/8/21 14:00:48
所 在 地:中國大陸
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【塑化劑檢測(cè)試劑盒】齊一生物您實(shí)驗(yàn)的好伙伴.感謝您對(duì)齊一生物科技的信任和支持.齊一生物為您提供品質(zhì)的產(chǎn)品和*優(yōu)質(zhì)的服務(wù)。代理品牌CUSABIO Randox-lifescience Santa Abcam jackson Sigma Amresco Qiagen Cayman millipore invitrogen merk ebioscience prospec歡迎廣大客戶咨詢,齊一生物另有大量宣傳海報(bào)和小禮品贈(zèng)送。網(wǎng)站:www.qiyibio.com
齊一生物銷售:021-6034 8496;181214 53965;173021 04490【塑化劑檢測(cè)試劑盒】
4502103 artus VZV TM PCR Kit (24) RUO CNY
133271 NeXtalStock PIPES pH 7.0 (200) CNY
133270 NeXtalStock Phosphate-citr. pH 5.2 (200) CNY 【塑化劑檢測(cè)試劑盒】
990512 Filter-Tips, 50 µl (960) CNY
337620 qBiomarker SYBR Green Fluor Mastermix(2) CNY
337011 qBiomarker Somatic Mutations PCR Assays CNY
4500263 artus HSV-1/2 RG PCR Kit (24) CE CNY
939016 Buffer ATL ( 4 x 50 ml),GPR CNY
4500163 artus HSV-1/2 TM PCR Kit (24) CE CNY
1073925 Ni-NTA Superflow (8 x 500 ml),cus,G CNY
9010931 BGR Greifer P7 (alt) CNY
9010858 BGR DT-Abstreifer 8-fach P7xxx D CNY
931036 QIAsymphony Virus/Bact Mini Kit (192) CNY
133248 NeXtalStock Sodium succinate pH6.5 (200) CNY
330603 RT² SYBR Green FAST Mastermix (24) CNY
929608 QX Pro Separation Buffer (40 ml) CNY
5000-1415 Knob RB671CSKWL Matte, VTX2 CNY
5000-1408 Cable Shielded 1/17HP, VTX2 CNY
L2170 hc2 CT/GC HC2 DNA Test PI (CD-ROM) CNY 【塑化劑檢測(cè)試劑盒】
L1971 Rotary Shaker User's Manual CNY
9240705 O-ring Kit, Capper, Spindle, AP CNY
9240693 Actril Sterilant & Test Strips, AP CNY
9243653 Comprehen 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
386516 Investigator STR GO! Lysis Buffer (200) CNY
208256 QuantiNova Probe PCR Kit (2500) CNY
208254 QuantiNova Probe PCR Kit (500) CNY
180984 GeneRead Adapter I Set 12plex (72) CNY
614035 careHPV Test, SFDA (96-test) CNY
282605 virotype Influenza A RT-PCR Kit (96) CNY
272703 pigtype PRRSV Ab (5) CNY
273003 pigtype Salmonella Ab (5) CNY
280377 virotype BVDV RT-PCR Kit (480) CNY
9018462 Marker Kit, QC tool, QX CNY
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