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人抗流行性出血热病毒抗体IgG(EHF)ELISA试剂盒现货
点击次数:10发布时间:2016/8/14 17:24:34
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更新日期:2016/8/14 17:24:34
所 在 地:中国大陆
产品型号:
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详细内容
Linco 公司主要致力于糖尿病与肥胖症研究及相关领域的新产品研发,以为广大研究人员提供值得信赖的高品质产品而自豪。在Luminex技术基础上开发出的LINCOplexTM系列产品,可以在一份25ul的样品中同时定量检测多种蛋白质分子。该系列包括人、小鼠和大鼠细胞因子检测试剂盒、apolipoproteins检测试剂盒和内分泌检测试剂盒,其中的细胞因子检测试剂盒可以根据客户的研究需要灵活提供(*少3种细胞因子)。Linco公司还在不断努力,为该系列试剂盒提供更多的检测指标。
http://www.millipore.com/index.do
Molecular Probes,作为Invitrogen的全资子公司,是全球*主要的用于的生物医药和其他科学研究的荧光检测产品的供货商,应用于基因组学,蛋白质组学及细胞生物学标记等方面,服务于全球的商业机构和科学实验室。自1975年成立以来,作为荧光技术的先锋,已经实现了基于持续的革新、卓越的服务和客户高满意度之上的高速增长。Molecular Probes已建立了多达3000种的荧光探针和生物化学品的生产线,使得在诸如分子和细胞生物、免疫学、生物化学和神经科学等不同领域的研究项目成为可能。
http://www.invitrogen.com/site/us/en/home.html
【人抗流行性出血热病毒抗体IgG(EHF)ELISA试剂盒现货】MBL 成立于1969年,是日本家抗体生产商。
公司早期致力于研究生产血浆蛋白质抗体,是抗体研究、发展和生产的先锋者。现在,公司提供3000多种细胞骨架、致癌基因产品和信号转导蛋白质抗体。MBL的自身免疫性疾病的诊断剂对医药界贡献非常大,该公司产品在自身免疫性疾病方面占据了日本国内市场80%的份额,在海外市场也同样受到欢迎。近年来,MBL大力引进重组DNA细胞和细胞融合技术来开发用于疾病诊断和疗效观察的诊断试剂。另外,公司开发了大量分子生物学和细胞生物学研究的产品,包括抗体和可溶性Fas ELISA试剂盒。
http://www.mblintl.com/
Merck 是生命科学领域的旗舰企业,拥有以下品牌:
Calbiochem corp. 为全球的信号转导类产品供应商。
Stratagene Cloning System. Stratagene产品涉及到分子生物学、蛋白质组学、药物研发等领域。
Oncogen 产品集中在细胞凋亡及周期研究领域,产品专而精。
Novagen 产品线从上游的基因及蛋白分离到表达、分析、纯化,覆盖面宽。
http://www.merck.com.cn/zh/index.html
【人抗流行性出血热病毒抗体IgG(EHF)ELISA试剂盒现货】Millipore 产品以纯水以及过滤相关产品为主,是目前纯水市场上的绝对领导者。2006年,Millipore又合并了生物试剂的知名公司Serologicals,从而获得了其旗下Upstate(信号转导、药物筛选专家)、Chemicon(干细胞和神经生物学专家)以及Linco(内分泌检测专家)的全部产品和技术等。从而成为生物界更全而有实力的供应商。
http://www.millipore.com/
Miltenyi (美天妮) 德国美天旎公司是一个以细胞分选技术为主、拥有多样化产品的生物技术公司。主要开发研制并销售世界上的细胞分选、细胞生物学、相关分子生物学产品和技术,尤其在干细胞分选、DC细胞分选与分析、细胞因子分泌细胞分选与分析、免疫治疗、再生医学方面占有极大的优势。CD133、BDCA-2(CD303)、BDCA-4(CD304)单抗均为其产品。
http://www.miltenyibiotec.com/en/default.aspx
NEB (New England Biolabs, Inc.)成立于20世纪70年代,致力于生化酶类及其它相关试剂的研发和生产。经过20多年的不懈努力, NEB凭借其高品质的产品、一流的专业服务,已成为限制性内切酶及相关产品*佳供应商。到目前为止,NEB可提供210多种内切酶,其中有130多种内切酶为重组酶。克隆及重组技术的运用,使NEB能在提高内切酶的纯度及品质的同时,极大地削减生产费用,从而为用户提供价格更合理、品质更优良的产品。NEB将通过不懈努力,在内切酶及相关领域继续保持地位,为客户提供更多更好的产品和更专业的服务。
http://www.neb-china.com/
【人抗流行性出血热病毒抗体IgG(EHF)ELISA试剂盒现货】Novus 位于美国科罗拉多州,是一家著名的抗体公司。公司的愿景是提供优质的产品,完善的客户服务以帮助客户快速找到*适合的抗体产品。通过全球代理商和网络提供10000多种研究级抗体,涉及生命科学的各个领域。
http://www.novusbio.com/
PeproTech 位于英国, 在美国也有公司。成立12年来,公司已开发了200种以上的重组细胞因子和相关抗体.所有产品以冻干形式提供,以方便运输和储存.目前公司正在扩大产品线,生产抗原亲和多抗及其生物素标记物,ELISA试剂盒和新型抗体。主要以小包装的细胞因子受广大研究生客户喜爱。【人抗流行性出血热病毒抗体IgG(EHF)ELISA试剂盒现货】
http://www.peprotech.com/
PhytoTech lab 美国著名的植物培养基供应商,公司集研发、生产、销售为一体,产品主要覆盖植物组织培养、植物生物技术与植物科学等领域。特色产品有优质 MURASHIGE & SKOOG (MS) 基础培养基、植物凝胶、琼脂粉、植物生长调节因子、抗生素等。
http://www.phytotechlab.com/
QY-x2031 CoC1 卵巢癌 1640+10%胎牛血清
QY-x2032 CoC2 卵巢癌 1640+10%胎牛血清
QY-x2033 OVCAR-3 卵巢癌 DMEM+10%胎牛血清
QY-x2034 SK-OV-3 卵巢腺癌 1640+10%胎牛血清 【人抗流行性出血热病毒抗体IgG(EHF)ELISA试剂盒现货】
QY-x2035 SK-OV-3/DDP 卵巢腺癌顺铂耐药株 1640+10%胎牛血清
QY-x2036 HeLa 宫颈癌 1640+10%胎牛血清
QY-x2037 HeLaS3 宫颈癌 1640+10%胎牛血清
QY-x2038 HEC-1B 子宫内膜癌
QY-x2039 JEG-3 绒癌 1640+10%胎牛血清
QY-x2040 Du145 前列腺癌 高糖DMEM+10%胎牛血清
QY-x2041 LNCaP 前列腺癌
QY-x2042 LNCaP clone 前列腺癌
QY-x2043 PC-3 前列腺癌 DMEM+10%胎牛血清
QY-x2044 Tsu-pr1 非雄激素依赖型前列腺癌 1640+10%胎牛血清
QY-x2045 HOS 骨肉瘤 MEM+非必需氨基酸+10%胎牛血清
QY-x2046 MG-63 成骨肉瘤 MEM+非必需氨基酸+10%胎牛血清
QY-x2047 Saos-2 骨肉瘤 1640+10%胎牛血清
QY-x2048 U-2OS 骨肉瘤 1640+10%胎牛血清
QY-x2049 OS-732 骨肉瘤 1640+10%胎牛血清 瘤株
QY-x2050 A-204 横纹肌肉瘤 【人抗流行性出血热病毒抗体IgG(EHF)ELISA试剂盒现货】
QY-x2051 HT1080 纤维肉瘤 1640+10%胎牛血清
QY-x2052 A375 皮肤黑色素瘤 DMEM+10%胎牛血清
QY-x2053 细胞中心实验室细胞库部分细胞系目录(鼠类肿瘤细胞)
QY-x2054 1.小鼠类
QY-x2055 细胞名称 组织类型 培养条件
QY-x2056 Lewis 肺癌 瘤株
QY-x2057 LA795 肺腺癌 瘤株
QY-x2058 EAC 艾氏腹水瘤 瘤株
QY-x2059 S180 腹水瘤 瘤株
QY-x2060 H22 肝癌 瘤株
QY-x2061 H22 肝癌 1640+10%胎牛血清 体外培养株
9241769 QIAxtractor, Full Agreement The Full Agreement, QIAxtractor provides full service coverage for the QIAxtractor and the CAS 1280. Costs for service visits are fully covered including travel, labor, and parts. One on-site pipetting head service and inspection is included . With a Full Agreement, there is a priority response time of 48 hours (2 working days). CNY
9241368 Interlock, IL1, EZ1a CNY
9241366 Cable, UV lamp voltage converter, EZ1a CNY
9240762 Co-Processor, AP96 CNY 【人抗流行性出血热病毒抗体IgG(EHF)ELISA试剂盒现货】
9240760 Update, Bucket/Elevator Head, AP196/98 CNY
9243549 Pyro Q96 MD, PM Service "Service response time (repair): not applicable
Periodic inspection/maintenance: yes
Inspection/maintenance delivery: onsite
Cost coverage for Repair Parts : not included
Cost coverage for labor: yes, full coverage
Cost coverage for travel: yes, full coverage
Replacement system (Loaner) provision: not applicable
Transportation cost coverage: yes, full coverage" CNY
9242786 RCS, Full Agreement, 2PM "Repair service delivery: onsite and to Regional Repair Center
Service response time (repair): 48 hours/2 business days or 7-10 working days for RRC repairs
Periodic inspection/maintenance: yes, 2/agreement year
Inspection/maintenance delivery: onsite for RCS only
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: yes, included" CNY
9242714 Validation Support, 5d, QIAgility The QIAGEN QIAgility Accelerated Validation Support service includes all travel and labor charges for a site visit up to 5 days by a QIAGEN Specialist. A QIAGEN specialist will provide an introduction to the QIAgility system and software, review the User Manual, as well as hands-on user support and QIAgility instrument operation. The Accelerated Validation service includes guidance on the laboratory’s validation experimental design, internal validation documentation support, and QIAGEN sponsored data templates. The QIAGEN Specialist will support the customer by running samples through the QIAGEN-only extraction method/system (does not include phenol-chloroform or similar methods), as well as general wet lab support such as pipetting for quantification, STR and CE setup, normalization, etc. to produce the data needed for the validation study. The customer is responsible for submitting the data to QIAGEN for assisted data analysis. The customer is responsible for final documentation and report using QIAGEN prepared templates provided with the final product. Enough consumable chemistry and accessories (QIAGEN or other vendors) should be purchased to cover the validation experimental design and are not included in the cost of validation support. Please indicate which processes (quant setup, normalization, PCR setup, CE setup) and kit manufacturer (Applied Biosystems, Promega, QIAGEN) need to be included in the validation. CNY
9242531 QIAsymphony SPAS, PM Agreement CNY
9242546 Probe Holder Assembly, LX200, LC CNY
9242152 Upgrade, CAS1820 vacuum DX/VX "The Upgrade, CAS 1820 vacuum DX/VX upgrades the X-tractorgene to use the improved vacuum system for the QIAxtractor. The upgrade is conducted as an on-site service, performed by a QIAGEN service specialist.
The upgrade allows for the usage of the QIAGEN DX and VX capture plates and the disposable silicon mats.
During the service, the new vacuum system is installed and the software is updated. Please note that due to the software upgrade the instrument will only run the QIAxtractor software applications. Customized run files from the previous version will have to be adapted beforehand for additional fees." CNY
5000-1404 Plate Cartridge 110V, VTX2 CNY
5000-1277 Top Housing W LID, DML2 CNY
5050-1029 Mouse, PC System spare CNY
5025-1011 Expand 4 Pipettor 240V CNY
9240747 Belt, Reagent Pump 117 groove, AP CNY
9240720 Cable Carrier, Tubing, Dispense Head, AP CNY
9240700 Tubing, Waste, 1 1\4", AP CNY
9243690 DML Luminometer, Repair Fee DML Repair Fee covers Regional Repair Center service for non-service agreement covered DML 2000 and DML 3000 units. Includes labor, parts and shipping materials. CNY
9243652 Comprehen Valid., QuantiPlex/QP Hyres """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 【人抗流行性出血热病毒抗体IgG(EHF)ELISA试剂盒现货】
6000-3101 Rapid Capture System CNY
19134 QIAGEN Proteinase K CNY
614033 careHPV Test, SFDA (24-test) CNY
274203 flocktype IBDV Ab (5) CNY
270803 cattletype MAP Ab (5) CNY
280303 cador BVDV RT-PCR Kit (24) CNY
282303 virotype PRRSV RT-PCR Kit (24) CNY
282305 virotype PRRSV RT-PCR Kit (96) CNY
280443 virotype BTV pan/8 RT-PCR Kit (24) CNY
939012 Buffer N2 (2 x 10 ml) CNY
871105 EGFR PCR Kit (100) CNY
800382 Restriction Map CNY
871005 KRAS PCR Kit (100) CNY