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人抗流行性出血熱病毒抗體IgG(EHF)ELISA試劑盒現貨
點擊次數:10發布時間:2016/8/14 17:24:34

更新日期:2016/8/14 17:24:34
所 在 地:中國大陸
產品型號:
優質供應
詳細內容
Linco 公司主要致力于糖尿病與肥胖癥研究及相關領域的新產品研發,以為廣大研究人員提供值得信賴的高品質產品而自豪。在Luminex技術基礎上開發出的LINCOplexTM系列產品,可以在一份25ul的樣品中同時定量檢測多種蛋白質分子。該系列包括人、小鼠和大鼠細胞因子檢測試劑盒、apolipoproteins檢測試劑盒和內分泌檢測試劑盒,其中的細胞因子檢測試劑盒可以根據客戶的研究需要靈活提供(*少3種細胞因子)。Linco公司還在不斷努力,為該系列試劑盒提供更多的檢測指標。
http://www.millipore.com/index.do
Molecular Probes,作為Invitrogen的全資子公司,是全球*主要的用于的生物醫藥和其他科學研究的熒光檢測產品的供貨商,應用于基因組學,蛋白質組學及細胞生物學標記等方面,服務于全球的商業機構和科學實驗室。自1975年成立以來,作為熒光技術的先鋒,已經實現了基于持續的革新、卓越的服務和客戶高滿意度之上的高速增長。Molecular Probes已建立了多達3000種的熒光探針和生物化學品的生產線,使得在諸如分子和細胞生物、免疫學、生物化學和神經科學等不同領域的研究項目成為可能。
http://www.invitrogen.com/site/us/en/home.html
【人抗流行性出血熱病毒抗體IgG(EHF)ELISA試劑盒現貨】MBL 成立于1969年,是日本家抗體生產商。
公司早期致力于研究生產血漿蛋白質抗體,是抗體研究、發展和生產的先鋒者,F在,公司提供3000多種細胞骨架、致癌基因產品和信號轉導蛋白質抗體。MBL的自身免疫性疾病的診斷劑對醫藥界貢獻非常大,該公司產品在自身免疫性疾病方面占據了日本國內市場80%的份額,在海外市場也同樣受到歡迎。近年來,MBL大力引進重組DNA細胞和細胞融合技術來開發用于疾病診斷和療效觀察的診斷試劑。另外,公司開發了大量分子生物學和細胞生物學研究的產品,包括抗體和可溶性Fas ELISA試劑盒。
http://www.mblintl.com/
Merck 是生命科學領域的旗艦企業,擁有以下品牌:
Calbiochem corp. 為全球的信號轉導類產品供應商。
Stratagene Cloning System. Stratagene產品涉及到分子生物學、蛋白質組學、藥物研發等領域。
Oncogen 產品集中在細胞凋亡及周期研究領域,產品專而精。
Novagen 產品線從上游的基因及蛋白分離到表達、分析、純化,覆蓋面寬。
http://www.merck.com.cn/zh/index.html
【人抗流行性出血熱病毒抗體IgG(EHF)ELISA試劑盒現貨】Millipore 產品以純水以及過濾相關產品為主,是目前純水市場上的絕對領導者。2006年,Millipore又合并了生物試劑的知名公司Serologicals,從而獲得了其旗下Upstate(信號轉導、藥物篩選專家)、Chemicon(干細胞和神經生物學專家)以及Linco(內分泌檢測專家)的全部產品和技術等。從而成為生物界更全而有實力的供應商。
http://www.millipore.com/
Miltenyi (美天妮) 德國美天旎公司是一個以細胞分選技術為主、擁有多樣化產品的生物技術公司。主要開發研制并銷售世界上的細胞分選、細胞生物學、相關分子生物學產品和技術,尤其在干細胞分選、DC細胞分選與分析、細胞因子分泌細胞分選與分析、免疫治療、再生醫學方面占有極大的優勢。CD133、BDCA-2(CD303)、BDCA-4(CD304)單抗均為其產品。
http://www.miltenyibiotec.com/en/default.aspx
NEB (New England Biolabs, Inc.)成立于20世紀70年代,致力于生化酶類及其它相關試劑的研發和生產。經過20多年的不懈努力, NEB憑借其高品質的產品、一流的專業服務,已成為限制性內切酶及相關產品*佳供應商。到目前為止,NEB可提供210多種內切酶,其中有130多種內切酶為重組酶?寺〖爸亟M技術的運用,使NEB能在提高內切酶的純度及品質的同時,極大地削減生產費用,從而為用戶提供價格更合理、品質更優良的產品。NEB將通過不懈努力,在內切酶及相關領域繼續保持地位,為客戶提供更多更好的產品和更專業的服務。
http://www.neb-china.com/
【人抗流行性出血熱病毒抗體IgG(EHF)ELISA試劑盒現貨】Novus 位于美國科羅拉多州,是一家著名的抗體公司。公司的愿景是提供優質的產品,完善的客戶服務以幫助客戶快速找到*適合的抗體產品。通過全球代理商和網絡提供10000多種研究級抗體,涉及生命科學的各個領域。
http://www.novusbio.com/
PeproTech 位于英國, 在美國也有公司。成立12年來,公司已開發了200種以上的重組細胞因子和相關抗體.所有產品以凍干形式提供,以方便運輸和儲存.目前公司正在擴大產品線,生產抗原親和多抗及其生物素標記物,ELISA試劑盒和新型抗體。主要以小包裝的細胞因子受廣大研究生客戶喜愛。【人抗流行性出血熱病毒抗體IgG(EHF)ELISA試劑盒現貨】
http://www.peprotech.com/
PhytoTech lab 美國著名的植物培養基供應商,公司集研發、生產、銷售為一體,產品主要覆蓋植物組織培養、植物生物技術與植物科學等領域。特色產品有優質 MURASHIGE & SKOOG (MS) 基礎培養基、植物凝膠、瓊脂粉、植物生長調節因子、抗生素等。
http://www.phytotechlab.com/
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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 【人抗流行性出血熱病毒抗體IgG(EHF)ELISA試劑盒現貨】
QY-x2035 SK-OV-3/DDP 卵巢腺癌順鉑耐藥株 1640+10%胎牛血清
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QY-x2037 HeLaS3 宮頸癌 1640+10%胎牛血清
QY-x2038 HEC-1B 子宮內膜癌
QY-x2039 JEG-3 絨癌 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 非雄激素依賴型前列腺癌 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 橫紋肌肉瘤 【人抗流行性出血熱病毒抗體IgG(EHF)ELISA試劑盒現貨】
QY-x2051 HT1080 纖維肉瘤 1640+10%胎牛血清
QY-x2052 A375 皮膚黑色素瘤 DMEM+10%胎牛血清
QY-x2053 細胞中心實驗室細胞庫部分細胞系目錄(鼠類腫瘤細胞)
QY-x2054 1.小鼠類
QY-x2055 細胞名稱 組織類型 培養條件
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 體外培養株
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 【人抗流行性出血熱病毒抗體IgG(EHF)ELISA試劑盒現貨】
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 【人抗流行性出血熱病毒抗體IgG(EHF)ELISA試劑盒現貨】
6000-3101 Rapid Capture System CNY
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