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您的位置:首页 > 产品展厅 >  化工原料 >  化学试剂 >  生化试剂 >  巨细胞病毒IgM抗体测定试剂盒

巨细胞病毒IgM抗体测定试剂盒

巨细胞病毒IgM抗体测定试剂盒

  • 价 格: 电议
  • 型号:
  • 生 产 地:中国大陆
  • 访问:20次
  • 发布日期:2016/6/20(更新日期:2016/8/27)

齐一生物科技(上海)有限公司

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QYBS6355 巨细胞病毒IgM抗体测定试剂盒 48T 供研究用
  • 详细内容
  • 公司简介
 巨细胞病毒IgM测定试剂盒齐一生物长期出售上万种进口试剂.对照品.药物杂质.中检所对照品.Sigma西格玛.美国BD.赛默飞thermofisher.日本wako.TCL.默克Merck .美国AMRESCO.Invitrogen.日本荣研化学株式会社.EP(欧洲药典).USP(美国药典).BP(英国药典).加拿大TRC.美国CaTO.标准品.对照品等保证原装产品,原装质量.到货快捷安全,专业的物流配送,专人全程跟踪订单,确保货物安全.准确.及时地送达指定地点.欢迎咨询齐一生物销售:0216034 8496181214 53965173021 04490

巨细胞病毒IgM测定试剂盒齐一生物专业代理Sigma西格玛.美国BD.赛默飞.日本wako.TCL.默克Merck .美国AMRESCO.日本荣研化学株式会社.EP(欧洲药典).USP(美国药典).BP(英国药典)加拿大TRC等试剂.标准品.对照品齐一生物销售:0216034 8496181214 53965173021 04490网站:www.qiyibio.com巨细胞病毒IgM测定试剂盒

 

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

9015599CD, Manual, Service, BIOROBOT 8000 IICNY

9015587EZ1 DNA Buffy Coat CardPre-programmed card for BioRobot EZ1 DNA Buffy Coat ProtocolCNY

 

9019166Lead screw - X, PyroQ96MDCNY


QY-x1140人肾上腺皮质腺癌细胞SW-13
QY-x1141人肾癌细胞系A498
QY-x1142人肾癌细胞系ACHN
QY-x1143人肾癌细胞GRC-1
QY-x1144人肾上皮细胞GES
QY-x1145人肾癌Wilms细胞G401
QY-x1146Asp2人胚胎肾细胞转化细胞FC33
QY-x1147人肾癌细胞SK-RC-42
QY-x1148人膀胱癌细胞EJ
QY-x1149人膀胱癌细胞5637(HTB-9)
QY-x1150人膀胱移行细胞癌细胞T24
QY-x1151人膀胱鳞癌细胞ScaBER
QY-x1152人膀胱癌细胞BIU-87
QY-x1153人胆管癌细胞RBE
QY-x1154人胆管癌细胞QBC939
QY-x1155人乳腺癌细胞MCF-7
QY-x1156人乳腺癌细胞MCF-7(NEW)
QY-x1157人乳腺癌细胞MCF-7(OLD)
QY-x1158人乳腺癌细胞MCF-7/ER36
QY-x1159人乳腺癌细胞(耐阿霉素)MCF-7/ADR
QY-x1160人乳腺癌细胞MCF-7B
QY-x1161人乳腺癌细胞SKBr-2HL
QY-x1162人乳腺癌细胞ZR75-1
QY-x1163人乳腺癌细胞ZR75-30
QY-x1164人乳腺癌细胞MDA-MB-231
QY-x1165人乳腺癌细胞MDA-MB-468
QY-x1166人乳腺癌细胞Hs-578T
QY-x1167人乳腺癌细胞HCC1937
QY-x1168人乳腺癌细胞MDA-MB-415
QY-x1169人乳腺癌高转移细胞MDA-MB-435
QY-x1170人乳腺癌细胞MDA-MB-435S
 

科研之路,您我并肩同行!齐一生物具有完善的ELISA试剂盒开发平台,成熟的抗原、抗体研发系统,熟练掌握各种酶联技术,如双抗夹心法、(直接)竞争法、间接竞争法、阻断法、间接法、双抗原夹心法等方法,结合我公司的诊断试剂开发团队我们可以有效的将试剂盒开发为临床诊断级别,质量处于全国前茅。齐一生物针对中高端客户推出自主品牌QIYBO试剂盒为了保证客户用货质量,我公司采用纯进口原料现包被生产,质量稳定高.
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