产品介绍
大鼠热休克蛋白70(HSP-70)ELISA试剂盒厂家
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发布日期:2016/8/5 22:43:31
更新日期:2016/8/5 22:43:31
详细内容
【大鼠热休克蛋白70(HSP-70)ELISA试剂盒厂家】齐一生物科技(上海)有限公司专业的供应商,提供报价,咨询,技术服务,欢迎来电齐一生物销售:021-6034 8496;181214 53965;173021 04490咨询选购。【大鼠热休克蛋白70(HSP-70)ELISA试剂盒厂家】齐一生物www.qiyibio.com 供应进口elisa试剂盒、elisa试剂盒,分子学试剂盒,免疫组化试剂盒,rna提取试剂盒,质粒提取试剂盒全套供应价格实惠,现货充足
QY-x983 人胰腺细胞AR42J 【大鼠热休克蛋白70(HSP-70)ELISA试剂盒厂家】
QY-x984 人胰腺癌细胞MIApaca-2
QY-x985 人胰腺癌细胞JF-305
QY-x986 人胰腺癌细胞PC-2
QY-x987 人胰腺癌细胞SW1990
QY-x988 人胰腺癌细胞CaPan-Ⅱ/Capan-2
QY-x989 人胰腺癌细胞CRL
QY-x990 人胰腺癌细胞SFPAC-1
QY-x991 人胚胎胰腺组织来源细胞CCC-HPE-2
QY-x992 人胰腺腺泡上皮癌HPAC
QY-x993 人胰腺腺癌细胞 Panc 10.05
QY-x994 人肝癌细胞HepG-2
QY-x995 人肝癌细胞HepG2.2.1.5
QY-x996 人肝癌细胞SMMC-7721
QY-x997 人肝癌细胞QGY-7701
QY-x998 人肝癌细胞QGY-7703
QY-x999 人肝癌细胞Bel-7402 【大鼠热休克蛋白70(HSP-70)ELISA试剂盒厂家】
QY-x1000 人肝癌细胞Bel-7405
QY-x1001 人肝癌细胞Hep3B2.1-7
QY-x1002 人肝癌细胞SK-HEP-1
QY-x1003 人肝癌亚力山大细胞HCCC-9810
QY-x1004 人胆囊癌细胞GBC-SD
QY-x1005 正常人肝细胞L-02
QY-x1006 人胚肝细胞正常QSG-7701
QY-x1007 人肝细胞正常HL-7702
QY-x1008 CCL13张氏肝细胞正常Chang liver
QY-x1009 人肝星形细胞正常LX-2
QY-x1010 人肝内胆管上皮细胞HIBEpiC
QY-x1011 人高转移肝癌细胞LM3
QY-x1012 人肝癌细胞系LM-6
3QY-x1013 人低转移肝癌细胞MHCC97-L
9022322 Power Supply, Controller, careHPV CNY
9022121 Tool. Rotor Hub Height Jig, RGQ CNY
9021404 RGQ MDx User manuals for IVD use(Europe) CNY
9238610 Collet chuck CNY
9238479 Motor, syringe, RapidPlate CNY
9238152 Elution Microplate Adapter 8000, SBS CNY
9237932 Syringe, 100µl CNY 【大鼠热休克蛋白70(HSP-70)ELISA试剂盒厂家】
9240663 Nut, Flangeless,1/4-28, Black, AP CNY
9240634 Power Supply, Main PCB, Aztec, AP196/98 CNY
9240630 Power Supply, 5VDC 1.5 AMP, AP96 CNY
9240593 Unload Valve, Pump, Pressure, AP196/98 CNY
9240562 Fuse, PCB, 315, Eppendorf, AP196/98 CNY
9240536 Motor Assy, SiNug, 17, All, AP96/196 CNY
9240514 CD R/W, AP196/98 CNY
9240504 PC-104, AP98 CNY
9240346 Autopure, Full Agreement "Repair service delivery: onsite
Service response time (repair): 48 hours/2 business days
Periodic inspection/maintenance: yes, 1/agreement year
Inspection/maintenance delivery: onsite
Cost coverage for repair parts: yes, included
Cost coverage for labor: yes, included
Cost coverage for travel: yes, included
Replacement system (Loaner) provision: not included
Transportation cost coverage: not applicable" CNY
9240098 Re-Installation, BR EZ1 The Re-Installation, BR EZ1 facilitates quick implementation of system back into lab routine by minimizing instrument set-up phase. It covers hardware and software check of instrument and provides user with operator refesher overview. Re-installation includes labor and travel costs. Re-installation performance process is documented on a GMP/GLP-compliant Field Service document. CNY
9239852 Foot bumpers, v2.0 (4) CNY
9019944 Cable, P-axis, wires, 8 ch. , C18 CNY
9238880 Bearings up. & low, BS96 CNY
9238836 BioSprint96, Basic Agreement, no PM "Repair service delivery: onsite
Service response time (repair): 5 business days
Periodic inspection/maintenance: not included
Inspection/maintenance delivery: not applicable
Cost coverage for Repair Parts : yes, full coverage
Cost coverage for labor: yes, full coverage
Cost coverage for travel: yes, full coverage
Replacement system (Loaner) provision: not applicable
Transportation cost coverage: not applicable" CNY
9241211 Full Agreement Depot Repair, DML2000, 1y "The Full Agreement Depot Repair, DML2000 provides full service coverage for the DML 2000 luminometer. 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
9241191 Magnet, tool, QX CNY 【大鼠热休克蛋白70(HSP-70)ELISA试剂盒厂家】
9238825 Spare bucket for plate rotor CNY
9238815 Rect. carrier for 12 tubes 10 ml w/ cap CNY
9019472 TAPE SPACER CLEAR GS CNY
9019464 UV tube, Cxx CNY
9243650 Comprehen 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
9237333 Install, BR plus 3 integr. w. scheduling Installation and training, BioRobot System including three approved integration devices with scheduling CNY
9237328 Upgrade, BR & 2 ext. devices w. sched. Upgrade BioRobot with two approved integration devices using scheduling software CNY
9237173 Shield, V-housing CNY
9233208 Tubing, liquid system 2.5/1.5 CNY
9237155 V-Housing with Sample Needle CNY