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【Cathepsin D Inhibitor Screening Kit (Fluorometric)】齐一生物科技(上海)有限公司是一家专业销售生化检测试剂盒.酶联免疫试剂盒,抗体蛋白.生化试剂,标准品和对照品的大型化学科技公司.自公司成立以来,本着始终拥有的创业激情,公司的销售额保持高速增长,企业规模不断扩大. 齐一生物销售:021-6034 8496;181214 53965;173021 04490网址:www.qiyibio.com
9238854 #BR M96, Basic Agreement The Basic Cover Agreement M96 provides full service coverage for the BioRobot M96. Costs for service visits are fully covered including travel, labor, and parts. The agreement also includes one annual preventive maintenance visit, with costs for labor and parts covered. With a Basic Cover Agreement, the response time is 5 working days. CNY
9238842 RS232 box, non-online fill, RapidPlate CNY
9241215 Full Agreement Depot Repair, Shaker, 1yr "The Full Agreement Depot Repair, Shaker provides full service coverage for the plate shaker used in the digene HPV application. 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
9238833 #BR 9604, Basic Agreement The Basic Cover Agreement 9604, 1 PM provides full service coverage for the BioRobot 9604. Costs for service visits are fully covered including travel, labor, and parts. The agreement also includes one annual preventive maintenance visit, with costs for labor and parts covered. With a Basic Cover Agreement, the response time is 5 working days. CNY
9238832 BR 9600, Basic Agreement The Basic Cover Agreement 9600 provides full service coverage for the BioRobot 9600. Costs for service visits are fully covered including travel, labor, and parts. The agreement also includes one annual preventive maintenance visit, with costs for labor and parts covered. With a Basic Cover Agreement, the response time is 5 working days. CNY 【Cathepsin D Inhibitor Screening Kit (Fluorometric)】
9238819 Rect. carrier for 5 glass tubes 25ml CNY
9237527 Software LiquiChip Workstation IS V2.2. CNY
9237380 Installation, BR MDx & 2 react. setup Installation and training, including two customized reaction setup protocols CNY
9237379 Installation, BR MDx & 1 react. setup Installation and training, including one customized reaction setup protocol CNY
9237378 BR MDx, Installation The Installation, BR MDx facilitates the quick implementation of the BioRobot MDx into the lab routine by minimizing the instrument start-up phase. It covers the hardware and software installation of the BioRobot MDx instrument and provides the user with an introductory training on operation and user maintenance. The installation includes labor and travel costs. The performance of the installation process is documented on a GMP/GLP-compliant Field Service document. CNY
9237175 Guard Fan, Platic XYP CNY
9233209 Tubing, 3/2, CNY
9233155 Power Cord, European CNY
9236418 Board, CPU, TWI CNY
9236345 Red LSR CNY
9236166 Safety shield, RapidPlate CNY
9230863 Anpressplatte Rose-80 CNY
9235538 Teaching Tool CNY
9230282 Cable, RS323, robot to syringe pump, 225 CNY
5050-2002 hc2 Software V2 Package CNY
BS96RNA BioSprint 96 to RNA (384) - UDP CNY 【Cathepsin D Inhibitor Screening Kit (Fluorometric)】
9240730 Tubing, 1/4" OD, Red, AP CNY
9240713 Poly Muffler Kit, AP96/196 CNY
9240690 Bearings, Lead Screws, AP CNY
9243654 Comprehen Valid., Other Quant. 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). For planning purposes and to ensure a smooth process, the Customer is expected to have all materials on-hand and inventoried one (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
6000-5013 LumiCheck Plate User Package CNY
288103 bactotype Mycoplasma Mg/Ms PCR Kit (24) CNY
1048147 QIAamp Viral RNA Mini Accessory Set CNY
270043 cattletype BHV1 gB Ab (5) CNY
1019992 Buffer Set (RNeasy 96 BioRobot 9604 Kit CNY
273401 pigtype Toxoplasma Ab (1) CNY
QY-x1820 人神经母细胞瘤株 SY5Y
QY-x1821 人结肠腺癌 CaCo2
QY-x1822 中国仓鼠卵细胞 成纤维细胞 CHO
QY-x1823 中国仓鼠卵细胞GFP细胞 CHO-GFP
QY-x1824 人鼻咽癌细胞(低分化) CNE-2
QY-x1825 SV40病毒转化的非洲绿猴肾成纤维细胞 Cos7
QY-x1826 毛囊细胞 DPC 【Cathepsin D Inhibitor Screening Kit (Fluorometric)】
QY-x1827 人脐血内皮细胞 EVC304
QY-x1828 EMPM2
QY-x1829 小鼠乳腺癌细胞 EMT-6
QY-x1830 人永生化表皮细胞 Hacat
QY-x1831 人早幼白血病细胞 HC-60
QY-x1832 人宫颈癌细胞 hela
QY-x1833 Hela-LC3B
QY-x1834 人 肝细胞癌 上皮样 Hep G2
QY-x1835 人 喉鳞状细胞癌 Hep-2
QY-x1836 人原髓细胞白血病细胞 HL-60
QY-x1837 人腹膜间皮细胞株 HMrSV5
QY-x1838 HPME
QY-x1839 小鼠胚胎成纤维细胞 HSF1-/-
QY-x1840 小鼠胚胎成纤维细胞 HSF1+/+
QY-x1841 小鼠胚胎成纤维细胞 HSF1-/+
QY-x1842 人结肠癌 HT-29 【Cathepsin D Inhibitor Screening Kit (Fluorometric)】
QY-x1843 人脐静脉内皮细胞 HUVE(18)
QY-x1844 小鼠Lewis肺癌 LLC
QY-x1845 人乳腺癌 MCF7
QY-x1846 小鼠神经成纤维细胞瘤 N2a Albino mouse
QY-x1847 小鼠神经成纤维细胞瘤GFP N2a-GFP
QY-x1848 人大肺细胞癌细胞 NCIH460
QY-x1849 NIH小鼠成纤维细胞 NIH 3T3
QY-x1850 人卵巢癌细胞 OVCaR-3
QY-x1851 大鼠肾上腺髓质嗜铬细胞瘤 PC12
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