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大鼠结缔组织生长因子(CTGF)ELISA试剂盒
点击次数:15发布时间:2016/6/2 17:35:06
更新日期:2017/12/6 9:13:09
所 在 地:中国大陆
产品型号:
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详细内容
Pierce 公司是蛋白质化学、免疫学和层析等很多方面的先驱和领导者,主要产品包括:化学发光体和比色底物、分析试剂、荧光标记探针、酶联免疫分析试剂盒等。 现为Thermo Fisher Scientific生命科学部旗下产品。
http://www.piercenet.com/Default.cfm
Qiagen 核酸和蛋白纯化专家。质粒纯化、染色体DNA纯化、DNA胶回收、RNA纯化、核酸转染试剂、His标签蛋白纯化等。
http://www1.qiagen.com/Default.aspx
R&D 公司于1976年成立于美国,一直致力于各种细胞因子及其相关分子的生产研发,其生产的各种ELISA试剂盒、重组因子及抗体以其卓越的品质赢得了世界各国科研及临床诊断机构的青睐。 是全世界的细胞因子公司。该公司产品丰富涵盖了百余种细胞因子类ELISA试剂盒, 重组细胞因子类蛋白(209种之多)及相关的多达250余种单克隆、多克隆抗体;细胞凋亡、Caspase及胶原酶系列以及细胞因子类等热点领域。
http://www.rndsystems.com/ http://www.rndsystemschina.com.cn/
【大鼠结缔组织生长因子(CTGF)ELISA试剂盒】Roche 罗氏应用科学部(Roche Applied Science)做为罗氏诊断公司的业务部门,专业服务于全球科学研究领域用户。深受欢迎的FuGENE转染试剂、DIG地高辛核酸标记及杂交系统、TUNEL凋亡检测试剂、蛋白酶抑制剂药片等均为罗氏产品。
除实验室常用的生化及分子生物学产品外,罗氏应用科学部为客户提供一系列基因组学和蛋白质组学分子生物学研究系统解决方案,不断满足当今生命科学的研究应用需要;产品应用领域涉及基因检测、基因表达、基因沉默、基因测序等多个方面。
https://www.roche-applied-science.com/
Santa cruz 公司是世界上的抗体生产厂家,目前可提供的抗体种类多达两万多种,几乎覆盖了目前生命科学研究的各个*新领域,其每种抗体又有多个克隆可以选择,还提供一些对应蛋白标准品及相关产品,如ABC试剂盒,各种标记二抗,Western试剂盒,蛋白分子量Marker,核抽提物等,为免疫学研究工作提供了极大的方便。
http://www.scbt.com/
Sigma-Aldrich,Sigma 收购了Aldrich, Fuduka后,成为全球生化试剂厂家。Sigma-Aldrich集团是世界的化学/生物试剂供应商, 为进行研究的科学家和那些幻想着发现和治疗新的疾病的发明家们提供各种各样的化学/生物试剂。其试剂的应用面广,几乎涵盖工农业、科技、教育和技术产业各个部门,涉及生物、医药、化工、食品、材料等各个行业。Sigma-Aldrich集团公司以完整的产品线,优质的服务和良好的产品质量在世界范围内一直居地位。其产品数量超过120,000种。
http://www.sigmaaldrich.com.cn/china-mainland.html
Stressgen 是世界著名的以热休克蛋白研究突出的专业信号转导研究公司。
http://www.assaydesigns.com/
Tocris Bioscience 是高品质试剂提供商,共有2000多种产品,主要集中在神经科学和信号传导领域,产品类型包括小分子、多肽、抗体、配体和化合物筛选文库等,主要产品包括GPCR ligands,神经传递素,离子通道调控剂,信号通路抑制剂等,这些产品被广泛选择性地用于阻断或激活生物学通路。Tocris是世界上神经科学研究领域无可争议的领导者,其生产的影响神经系统的化学物质被多次引用,这些物质很多都来自Jeff Watkins(Tocris 的创立人)在Bristol大学原创性的研究工作。【大鼠结缔组织生长因子(CTGF)ELISA试剂盒】
http://www.tocris.com/
Thermo Fisher Scientific 生命科学部 是 Thermo Fisher Scientific 的主要部门,旗下产品线包括HyClone、Pierce、Endogen、Dharmacon、ABgene、Cellomics和Bioimage等。
Thermo Fisher Scientific生命科学部为生命科学和化学领域提供广泛的产品和服务,涵盖细胞培养、液体处理、蛋白质研究、RNA干扰、核酸扩增与生物贮存、高涵量细胞筛选与分析等领域。
http://www.thermo.com.cn/Default.aspx
【大鼠结缔组织生长因子(CTGF)ELISA试剂盒】Upstate 信号转导、药物筛选专家,主要产品有蛋白激酶与磷酸酶、蛋白质磷酸化位点特异性抗体、药物筛选、G蛋白偶联受体、染色质调控与基因印记学研究、组蛋白乙酰化抗体、染色质共沉淀抗体、神经生物学、细胞周期调控与细胞凋亡研究、脂分子信号调控、抗氧化损伤等。目前已被Millipore收购了。其抗体产品一直具有极强的特色。
http://www.millipore.com/
Vector Laboratories 公司是目前世界上著名的生物学检测试剂生产商。其产品主要包括ABC系列检测试剂盒、凝集素及各种来源和标记的二抗等,其产品质量优良,性能稳定。Vector公司于1977年率先开发出了生物素-亲和素系统,该产品系列是检测方法上的重要革命。其后,公司发展出ABC技术(Avidin : Biotinylated Enzyme Complex Technology,亲和素-生物素-过氧化物酶复合物技术),并建立了著名的VECTASTAIN?ABC系统,目前,该系统被视为*灵敏、*可靠与*有效的染色系统,并被广泛应用于免疫组织化学、免疫电镜、原位杂交与凝集素化学中。
http://www.vectorlabs.com/
Wako 日本和光纯药工业株式会社(Wako Pure Chemical Industries, Ltd) 创建于1922年,致力于提供实验用优质产品。目前产品达7万余种。【大鼠结缔组织生长因子(CTGF)ELISA试剂盒】
https://www.e-reagent.com/
Zymed Laboratories 公司位于美国生物科技重要城市南加州的圣迭亚哥市,目前是Invitrogen大家庭中的一员。是一家以生产免疫学检测试剂为主的综合性生物技术公司。Zymed公司的业务主要分为两大领域:生命科学和临床病理诊断。Zymed公司的所有产品反映了其在全球的自我定位策略-即一家重视质量、专注于全面解决问题的开发商、生产商和全球营销商。它在全球范围内为生命科学研究、临床研究、癌症诊断领域提供高质量的试剂和试剂盒。Zymed公司历史悠久,在抗体设计、开发、修饰、纯化和生产方面有21年的专业研究史。Zymed 公司得到 ISO 13485认证。
http://www.invitrogen.com/site/us/en/home.html
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9243650Comprehen 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
9237333Install, BR plus 3 integr. w. schedulingInstallation and training, BioRobot System including three approved integration devices with schedulingCNY
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92369163 Year Warranty, LiquiChipLiquiChip 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
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9015587EZ1 DNA Buffy Coat CardPre-programmed card for BioRobot EZ1 DNA Buffy Coat ProtocolCNY
9019166Lead screw - X, PyroQ96MDCNY