產品展示
Anti-NF-L（Neurofilament triplet L)低分子量神經絲蛋白抗體
點擊次數：12發布時間：2016/7/21 23:40:29
更新日期：2016/7/21 23:40:29
所 在 地：中國大陸
產品型號：
優質供應
詳細內容
【Anti-NF-L（Neurofilament triplet L)低分子量神經絲蛋白抗體】齊一生物科技（上海）有限公司經營試劑種類眾多：覆蓋分析化學品,無機化學品,有機化學品,生物化學品,材料化學品等.試劑信息齊全：包含試劑特性描述,詳細質量信息,應用方法.標準, 科研 用途以及正在開發的前沿應用歡迎前來選購。齊一生物銷售：021－6034 8496；181214 53965；173021 04490網站：http://www.qiyibio.com
└ 心房肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 心室肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 心肌成纖維細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 心臟微血管內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 主動脈內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 主動脈平滑肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 臍靜脈內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 臍動脈內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 臍靜脈平滑肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 臍動脈平滑肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 大隱靜脈平滑肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 冠狀動脈內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 食管上皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 食管平滑肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 腸微血管內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 腸動脈內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 腸靜脈內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 小腸平滑肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 結腸平滑肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 直結腸平滑肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 小腸粘膜上皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 結腸粘膜上皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 直腸粘膜上皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 肝內膽管上皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 肝實質細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 肝動脈內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 肝動脈平滑肌細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 肝星形細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 肝竇內皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
└ 胃粘膜上皮細胞總DNA 1μg/1μl（10μg/20ug/50ug）
9240536 Motor Assy, SiNug, 17, All, AP96/196 CNY
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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
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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
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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
