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【整合素样金属蛋白酶与凝血酶1型-7(抗体)】齐一生物您实验的好伙伴为您提供“最高品质的产品”和“最优质的服务”
CUSABIORandox-lifescienceSantaAbcamjacksonSigmaAmrescoQiagenCaymanmilliporeinvitrogenmerkebioscienceprospec欢迎广大客户咨询,另有大量宣传海报和小礼品赠送. 齐一生物销售:021-6034 8496;181214 53965;173021 04490【整合素样金属蛋白酶与凝血酶1型-7(抗体)】
QY-x1690 人肺腺癌
QY-x1691 人肺癌细胞 SPC-A-1 肺癌 RPMI 1640 + 10% FBS
QY-x1692 人肺癌细
QY-x1693 人非小细胞肺癌细胞 A549 CCL-185? 肺癌 RPMI 1640 + 10% NBCS
QY-x1694 人肺癌细胞 GLC82 肺癌
QY-x1695 人小细胞肺癌细胞
QY-x1696 人肺鳞癌细胞 NCI-H446 HTB-171? 肺癌 RPMI 1640 + 10% NBCS
QY-x1697 人肺鳞癌细胞 NC1-H460 肺鳞癌 RPMI 1640 + 10% FBS
QY-x1698 鼠Lewis肺腺癌细胞(非小细胞) LLC 肺癌 RPMI 1640 + 10% FBS
QY-x1699 人胃腺癌细胞(低分化) BGC-823 胃癌 RPMI 1640 + 10% NBCS
QY-x1700 人胃癌细胞 NCI-N87 CRL-5822? 胃癌 RPMI 1640 + 10% FBS
QY-x1701 人胃癌细胞(未分化) HGC-27 胃癌 RPMI 1640 + 10% NBCS
QY-x1702 人乳腺癌细胞 MCF-7 HTB-22? 腺癌,乳腺,胸水。 DMEM+10%NBCS
QY-x1703 人乳腺癌细胞 MDA-MB-435S HTB-129? mammary gland; breast DMEM+10%NBCS 129&Template=cellBiology
QY-x1704 人宫颈癌细胞 HeLa CCL-2? 宫颈腺癌 DMEM+10%NBCS 【整合素样金属蛋白酶与凝血酶1型-7(抗体)】
QY-x1705 人结肠癌细胞 CaCo-2 HTB-37? 结肠癌 DMEM+10%FBS
QY-x1706 人胰腺癌细胞 PANC-1 CRL-1469? 胰腺;胰管;上皮细胞癌 DMEM+10%FBS
QY-x1707 人恶性黑色素瘤细胞 A-375 CRL-1619? 皮肤;恶性黑色素瘤 DMEM+10%NBCS
QY-x1708 鼠黑色素瘤细胞 B16-luc 黑色素瘤 RPMI 1640 + 10% NBCS
QY-x1709 人纤维肉瘤细胞 HT1080 CCL-121? 纤维肉瘤 MEM或 DMEM+10%FBS
QY-x1710 人原髓细胞白血病细胞(悬浮) HL-60 CCL-240? 外周血;早幼粒细胞;急性粒-单核细胞白血病 RPMI 1640 + 10% NBCS
QY-x1711 人T淋巴细胞白血病细胞(悬浮) Jurkat E6-1 TIB-152? T淋巴细胞;急性T细胞白血病 RPMI 1640 + 10% FBS
QY-x1712 人T淋巴细胞白血病细胞株
QY-x1713 大鼠或人主动脉平滑稽细胞A10
QY-x1714 大鼠肝细胞株BRL3A
QY-x1715 人慢性髓原白血病细胞系 K562 DMEM+10%NBCS
QY-x1716 草地贪夜
QY-x1717 蛾细胞 sf-21 蛾
QY-x1718 (昆虫) S900
QY-x1719 昆虫细胞 Sf-9 昆虫 S900
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
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 【整合素样金属蛋白酶与凝血酶1型-7(抗体)】
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
273505 pigtype Trichinella Ab (20) CNY
9019538 ZLVBelting, flat cogged, 6T, 2.5mm, CASx CNY
9020591 Tray Assembly, DML 3000 CNY
9021007 Motor, Pipettor X, DCU CNY
9013373 Fix kit, liquid handling, BR8000 CNY
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