产品展示
Anti-NF-L(Neurofilament triplet L)低分子量神经丝蛋白抗体
点击次数:12发布时间:2016/7/21 23:40:29
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更新日期:2016/7/21 23:40:29
所 在 地:中国大陆
产品型号:
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详细内容
【Anti-NF-L(Neurofilament triplet L)低分子量神经丝蛋白抗体】齐一生物科技(上海)有限公司经营试剂种类众多:覆盖分析化学品,无机化学品,有机化学品,生物化学品,材料化学品等.试剂信息齐全:包含试剂特性描述,详细质量信息,应用方法.标准, 科研 用途以及正在开发的前沿应用欢迎前来选购。齐一生物销售:021-6034 8496;181214 53965;173021 04490网站:http://www.qiyibio.com
└ 心房肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 心室肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 心肌成纤维细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 心脏微血管内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 主动脉内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 主动脉平滑肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 脐静脉内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 脐动脉内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 脐静脉平滑肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 脐动脉平滑肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 大隐静脉平滑肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 冠状动脉内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 食管上皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 食管平滑肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 肠微血管内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 肠动脉内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 肠静脉内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 小肠平滑肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 结肠平滑肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 直结肠平滑肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 小肠粘膜上皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 结肠粘膜上皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 直肠粘膜上皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 肝内胆管上皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 肝实质细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 肝动脉内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 肝动脉平滑肌细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 肝星形细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 肝窦内皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
└ 胃粘膜上皮细胞总DNA 1μg/1μl(10μg/20ug/50ug)
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
9238825 Spare bucket for plate rotor CNY 【Anti-NF-L(Neurofilament triplet L)低分子量神经丝蛋白抗体】
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
9237150 Heater Top CNY
9016151 #App. Package, M48, Pathology CNY
9019179 Opto - plate lock closed, PyroQ96MD CNY
9011883 Upgrade, high speed pipetting system CNY
9011882 Back unit, BR9600 CNY
9011823 Z-Modul; Tip-Adapter 300µl; BR8000 CNY
9236916 3 Year Warranty, LiquiChip LiquiChip 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