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广州市所在地
西班牙Certest乙型流感病毒单抗(克隆YB91)
广州健仑生物科技有限公司
广州健仑长期供应各种生物原料,主要代理品牌:西班牙Certest。
Certest Biotec,S.L. 是一家独立的生物技术公司,致力于人类临床领域的IVD诊断产品的开发和制造。快速检测是基于快速、准确和易于操作的诊断产品。 此外,Cerstest还有多种实时PCR产品,可以用于医院临床、实验室科研等。
Certest公司于2002年在萨拉戈萨成立,是一家创新技术型公司。公司的发展是基于新产品的开发、市场空间和机遇的探索,十几年来一直以高度专业化,以客户为导向,不断得创新,优化产品,专业知识,取得广大客户的信任和支持。Certest的质量体系已通过ISO 13485认证。
主要产品包括各种生物单克隆抗原抗体、重组蛋白。
轮状病毒单克隆抗体、腺病毒抗体、星状病毒单克隆抗体、诺如病毒单克隆抗体、幽门螺旋杆菌抗体、隐球菌抗体、肠道病毒抗体、贾第鞭毛虫抗体、弯曲杆菌抗体、阿米巴原虫抗体、呼吸道合胞病毒单抗等等。
西班牙Certest乙型流感病毒单抗(克隆YB91)
我司还提供其它进口或国产试剂盒:登革热、疟疾、流感、A链球菌、合胞病毒、腮病毒、乙脑、寨卡、黄热病、基孔肯雅热、克锥虫病、违禁品滥用、肺炎球菌、军团菌、化妆品检测、食品安全检测等试剂盒以及日本生研细菌分型诊断血清、德国SiFin诊断血清、丹麦SSI诊断血清等产品。
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西班牙Certest公司简介
Certest Biotec, S.L. is an independent biotechnology company devoted to the development and manufacturing of IVD diagnostic products in human clinical field. Our Rapid Test are based in a fast, reliable and easy-interpretation process. In addition, VIASURE contains a wide range of products for Real Time PCR that allow to identify the causal pathogens of the infectious diseases in physicians’ offices, labs and hospitals.
The company was established in Zaragoza in 2002 as an innovative and technology-based company. The company’s growth is based on the development of new products and the exploration for new market niches and opportunities. The key to understand its success is the way to understand its organization: highly specialised and customer-oriented based.
Mission, Vision, Values and Human Team
Mission
To develop, produce and market a wide range of innovative solutions and quality in vitro diagnostics for the detection of viruses, bacteria and parasites.
Vision
Being the international leader company in research and development for in vitro diagnostic solutions, increasing our distribution network through added value creation and company-customer trust.
Values
Customer orientation · Ethical behaviour · Teamwork · Continuous research and innovation ·Trained and motivated team · Quality and creativity in all processes
Human team
The multi-skilled team is a dedicated and experience professional group responsible for dealing with all the different company activities in an international environment.
Commitment to Innovation, Export and High-Technology.
Certest’s Quality System has been certified with ISO 13485.
One of the main objectives of Certest is to achieve customer satisfaction. For this, the management of the company ensures that customer requirements are determined and reviewed, identifying their needs and expectations, and translating them into requirements, all in order to maintain customer satisfaction.
See/Download the Certest Biotec ISO Standard Certification Certest Policy is consistent with its primary purpose, that of getting to all its products and services, quality and reliability, meeting the requirements and maintaining the effectiveness of the management system.
“Comparative study of two diagnostic tests for detection of RNA Zika Virus (ZIKV) in clinical samples”
“Comparison of Real-Time PCR test with the routine diagnosis technique to detect enteric pathogenic protozoa”
“Diagnostic of the Enteric Virus infection by Real-Time PCR in stool samples”
“Clinical performance evaluation of lyophilized VIASURE Real Time PCR Detection Kits for pathogen detection by participation in External Quality Assessment (EQA) programs”
“Detection and differentiation of Influenza A Virus, Influenza B Virus and H1N1 (pdm09) variant through an stabilized Real Time PCR Mix”
“Comparison of different molecular methods for the detection of non-influenza respiratory virus”virus”
【西班牙Certest生物原料】
货号 | 产品名称 | 规格 | 英文名称 |
MT-16R15 | 轮状病毒单克隆抗体(克隆R15) | x1mg | Anti-Rotavirus Mab (clone R15) |
MT-16R15s1 | 轮状病毒单克隆抗体(克隆R15) | x100μg | Anti-Rotavirus Mab (clone R15) |
MT-18A15 | 腺病毒抗体(克隆A15) | x1mg | Anti-Adenovirus Mab (clone A15) |
MT-18A15s1 | 腺病毒抗体(克隆A15) | x100μg | Anti-Adenovirus Mab (clone A15) |
MT-18AT18 | 星状病毒单克隆抗体(克隆AT18) | x1mg | Anti-Astrovirus Mab (clone AT18) |
MT-18AT18s1 | 星状病毒单克隆抗体(克隆AT18) | x100μg | Anti-Astrovirus Mab (clone AT18) |
MT-18AT8 | 星状病毒单克隆抗体(克隆AT8) | x1mg | Anti-Astrovirus Mab (clone AT8) |
MT-18AT8s1 | 星状病毒单克隆抗体(克隆AT8) | x100μg | Anti-Astrovirus Mab (clone AT8) |
MT-18NG28 | 诺如病毒GI单克隆抗体(克隆NG28) | x1mg | Anti-Norovirus GI Mab (clone NG28) |
MT-18NG28sl | 诺如病毒GI单克隆抗体(克隆NG28) | x100μg | Anti-Norovirus GI Mab (clone NG28) |
MT-18NP8 | 诺如病毒GII单克隆抗体(克隆NP8) | x1mg | Anti-Norovirus GII Mab (clone NP8) |
MT-18NP8sl | 诺如病毒GII单克隆抗体(克隆NP8) | x100μg | Anti-Norovirus GII Mab (clone NP8) |
MT-18EV5 | 肠道病毒抗体(克隆EV5) | x1mg | Anti-Enterovirus Mab (clone EV5) |
MT-18EV5sl | 肠道病毒抗体(克隆EV5) | x100μg | Anti-Enterovirus Mab (clone EV5) |
MT-16P2 | 幽门螺旋杆菌抗体(克隆P2)HP抗体 | x1mg | Anti-H. pylori Mab (clone P2) |
MT-16P2sl | 幽门螺旋杆菌抗体(克隆P2)HP抗体 | x100μg | Anti-H. pylori Mab (clone P2) |
MT-16GD10 | 艰难梭菌抗体(克隆GD10) | x1mg | Anti-GDH Mab (clone GD10) |
MT-16GD10sl | 艰难梭菌抗体(克隆GD10) | x100μg | Anti-GDH Mab (clone GD10) |
MT-18TA5 | 艰难梭菌毒素A抗(克隆TA5) | x1mg | Anti-CD Toxin A Mab (clone TA5) |
MT-18TA5sl | 艰难梭菌毒素A抗(克隆TA5) | x100μg | Anti-CD Toxin A Mab (clone TA5) |
MT-18TA7 | 艰难梭菌毒素A抗(克隆TA7) | x1mg | Anti-CD Toxin A Mab (clone TA7) |
MT-18TA7sl | 艰难梭菌毒素A抗(克隆TA7) | x100μg | Anti-CD Toxin A Mab (clone TA7) |
MT-18TB41 | 艰难梭菌毒素B抗(克隆TB41) | x1mg | Anti-CD Toxin B Mab (clone TB41) |
MT-18TB41sl | 艰难梭菌毒素B抗(克隆TB41) | x100μg | Anti-CD Toxin B Mab (clone TB41) |
MT-18TB48 | 艰难梭菌毒素B抗(克隆TB48) | x1mg | Anti-CD Toxin B Mab (clone TB48) |
MT-18TB48sl | 艰难梭菌毒素B抗(克隆TB48) | x100μg | Anti-CD Toxin B Mab (clone TB48) |
MT-18E10 | 大肠杆菌O157抗体(克隆E10) | x1mg | Anti-E. coli O157 Mab (clone E10) |
MT-18E10sl | 大肠杆菌O157抗体(克隆E10) | x100μg | Anti-E. coli O157 Mab (clone E10) |
MT-16CA29 | 弯曲杆菌抗体(克隆ECA29) | x1mg | Anti-Campylobacter Mab (clone CA29) |
MT-16CA29sl | 弯曲杆菌抗体(克隆ECA29) | x100μg | Anti-Campylobacter Mab (clone CA29) |
MT-18K31 | 隐球菌抗体(克隆K31) | x1mg | Anti-Crypto Mab (clone K31) |
MT-18K31sl | 隐球菌抗体(克隆K31) | x100μg | Anti-Crypto Mab (clone K31) |
MT-16G18 | 贾第鞭毛虫抗体(克隆G18) | x1mg | Anti-Giardia Mab trophozoite protein (clone G18) |
MT-16G18sl | 贾第鞭毛虫抗体(克隆G18) | x100μg | Anti-Giardia Mab trophozoite protein (clone G18) |
MT-16G22 | 贾第鞭毛虫抗体(克隆G22) | x1mg | Anti-Giardia Mab trophozoite protein (clone G22) |
MT-16G22sl | 贾第鞭毛虫抗体(克隆G22) | x100μg | Anti-Giardia Mab trophozoite protein (clone G22) |
MT-18EH30 | 阿米巴原虫抗体(克隆H30) | x1mg | Anti-Entamoeba Mab (clone EH30) |
MT-18EH30sl | 阿米巴原虫抗体(克隆H30) | x100μg | Anti-Entamoeba Mab (clone EH30) |
MT-16CP14 | 钙结合蛋白单克隆抗体(克隆CP14) | x1mg | Anti-Calprotectin Mab (clone CP14) |
MT-16CP14sl | 钙结合蛋白单克隆抗体(克隆CP14) | x100μg | Anti-Calprotectin Mab (clone CP14) |
MT-16F22 | 血红蛋白单抗(克隆F22) | x1mg | Anti-Haemoglobin Mab (clone F22) |
MT-16F22sl | 血红蛋白单抗(克隆F22) | x100μg | Anti-Haemoglobin Mab (clone F22) |
MT-16LC16 | 乳铁蛋白单抗(克隆LC16) | x1mg | Anti-Lactoferrin Mab (clone LC16) |
MT-16LC16sl | 乳铁蛋白单抗(克隆LC16) | x100μg | Anti-Lactoferrin Mab (clone LC16) |
MT-16LC4 | 乳铁蛋白单抗(克隆LC4) | x1mg | Anti-Lactoferrin Mab (clone LC4) |
MT-16LC4sl | 乳铁蛋白单抗(克隆LC4) | x100μg | Anti-Lactoferrin Mab (clone LC4) |
MT-26VP6 | 轮状病毒VP6重组蛋白 | x1mg | Rotavirus VP6 recombinant protein |
MT-26VP6 | 轮状病毒VP6重组蛋白 | x100μg | Rotavirus VP6 recombinant protein |
MT-25HEX | 腺病毒HEXON重组蛋白 | x1mg | Adenovirus HEXON recombinant protein |
MT-25HEXsl | 腺病毒HEXON重组蛋白 | x100μg | Adenovirus HEXON recombinant protein |
MT-25AST | 星状病毒衣壳重组蛋白 | x1mg | Astrovirus capsid recombinant protein |
MT-25ASTsl | 星状病毒衣壳重组蛋白 | x100μg | Astrovirus capsid recombinant protein |
MT-25NGI1 | 诺如病毒GI.1重组P结构域 | x1mg | Norovirus GI.1 recombinant P domain |
MT-25NGI1sl | 诺如病毒GI.1重组P结构域 | x100μg | Norovirus GI.1 recombinant P domain |
MT-25NGI3 | 诺如病毒GI.3重组P结构域 | x1mg | Norovirus GI.3 recombinant P domain |
MT-25NGI3sl | 诺如病毒GI.3重组P结构域 | x100μg | Norovirus GI.3 recombinant P domain |
MT-25NGII10 | 诺如病毒GII.10重组P结构域 | x1mg | Norovirus GII.10 recombinant P domain |
MT-25NGII10sl | 诺如病毒GII.10重组P结构域 | x100μg | Norovirus GII.10 recombinant P domain |
MT-25NGII17 | 诺如病毒GII.17重组P结构域 | x1mg | Norovirus GII.17 recombinant P domain |
MT-25NGII17sl | 诺如病毒GII.17重组P结构域 | x100μg | Norovirus GII.17 recombinant P domain |
MT-25NGII14 | 诺如病毒GII.4重组P结构域 | x1mg | Norovirus GII.4 recombinant P domain |
MT-25NGII14sl | 诺如病毒GII.4重组P结构域 | x100μg | Norovirus GII.4 recombinant P domain |
MT-25ETV | 肠道病毒VP1重组蛋白 | x1mg | Enterovirus VP1 recombinant protein |
MT-25ETVs1 | 肠道病毒VP1重组蛋白 | x100μg | Enterovirus VP1 recombinant protein |
MT-25PCH | 幽门螺杆菌重组外膜蛋白 | x1mg | H. pylori recombinant outer membrane protein |
MT-25PCHs1 | 幽门螺杆菌重组外膜蛋白 | x100μg | H. pylori recombinant outer membrane protein |
MT-25GDH | 艰难梭菌GDH重组蛋白 | x1mg | Clostridium difficile GDH recombinant protein |
MT-25GDHsl | 艰难梭菌GDH重组蛋白 | x100μg | Clostridium difficile GDH recombinant protein |
MT-24TXA | 艰难梭菌毒素A重组蛋白(无毒性片段) | x1mg | C. difficile Toxin A recombinant protein (fragment without toxic activity) |
MT-24TXAsl | 艰难梭菌毒素A重组蛋白(无毒性片段) | x100μg | C. difficile Toxin A recombinant protein (fragment without toxic activity) |
MT-24TXB | 艰难梭菌毒素B重组蛋白(无毒性片段) | x1mg | C. difficile Toxin B recombinant protein (fragment without toxic activity) |
MT-24TXBsl | 艰难梭菌毒素B重组蛋白(无毒性片段) | x100μg | C. difficile Toxin B recombinant protein (fragment without toxic activity) |
MT-25STX | 大肠杆菌O157 VT1重组蛋白 | x1mg | E. coli O157 VT1 recombinant protein |
MT-25STXsl | 大肠杆菌O157 VT1重组蛋白 | x100μg | E. coli O157 VT1 recombinant protein |
MT-25VT2 | 大肠杆菌O157 VT2重组蛋白 | x1mg | E. coli O157 VT2 recombinant protein |
MT-25VT2sl | 大肠杆菌O157 VT2重组蛋白 | x100μg | E. coli O157 VT2 recombinant protein |
MT-25CCP | 弯曲杆菌重组外膜蛋白 | x1mg | Campylobacter coli recombinant outer membrane protein |
MT-25CCPsl | 弯曲杆菌重组外膜蛋白 | x100μg | Campylobacter coli recombinant outer membrane protein |
MT-25CEP | 空肠弯曲杆菌重组外膜蛋白 | x1mg | Campylobacter jejuni recombinant outer membrane protein |
MT-25CEPsl | 空肠弯曲杆菌重组外膜蛋白 | x100μg | Campylobacter jejuni recombinant outer membrane protein |
MT-25A1G | 贾第虫肠道滋养体重组蛋白 | x1mg | Giardia intestinalis trophozoite recombinant protein |
MT-25A1Gsl | 贾第虫肠道滋养体重组蛋白 | x100μg | Giardia intestinalis trophozoite recombinant protein |
MT-25GCP | 贾第虫肠囊菌重组蛋白 | x1mg | Giardia intestinalis cyst recombinant protein |
MT-25GCPsl | 贾第虫肠囊菌重组蛋白 | x100μg | Giardia intestinalis cyst recombinant protein |
MT-25EDP | 内阿米巴重组蛋白 | x1mg | Entamoeba dispar recombinant protein |
MT-25EDPsl | 内阿米巴重组蛋白 | x100μg | Entamoeba dispar recombinant protein |
MT-25EHP | 溶组织内阿米巴重组蛋白 | x1mg | Entamoeba histolytica recombinant protein |
MT-25EHPsl | 溶组织内阿米巴重组蛋白 | x100μg | Entamoeba histolytica recombinant protein |
MT-25HCP | 人类钙卫蛋白重组蛋白 | x1mg | Human Calprotectin recombinant protein |
MT-25HCPs1 | 人类钙卫蛋白重组蛋白 | x100μg | Human Calprotectin recombinant protein |
MT-31NGA | 诺如病毒GI.1重组VLP | x1mg | Norovirus GI.1 recombinant VLP |
MT-31NGAsl | 诺如病毒GI.1重组VLP | x100μg | Norovirus GI.1 recombinant VLP |
MT-31NPA | 诺如病毒GII.4重组VLP | x1mg | Norovirus GII.4 recombinant VLP |
MT-31NPAsl | 诺如病毒GII.4重组VLP | x100μg | Norovirus GII.4 recombinant VLP |
MT-28PECU | 灭活的幽门螺杆菌抗原(天然提取物) | x1mg | Inactivated H. pylori antigen (native extract) |
MT-28PECUsl | 灭活的幽门螺杆菌抗原(天然提取物) | x100μg | Inactivated H. pylori antigen (native extract) |
MT-28EC7U | 灭活的大肠杆菌O157抗原(天然提取物) | x1mg | Inactivated E. coli O157 antigen (native extract) |
MT-28EC7Usl | 灭活的大肠杆菌O157抗原(天然提取物) | x100μg | Inactivated E. coli O157 antigen (native extract) |
MT-28CCU | 灭活的大肠杆菌抗原(天然提取物) | x1mg | Inactivated Campylobacter coli antigen (native extract) |
MT-28CCUsl | 灭活的大肠杆菌抗原(天然提取物) | x100μg | Inactivated Campylobacter coli antigen (native extract) |
MT-28CJU | 灭活的空肠弯曲杆菌抗原(天然提取物) | x1mg | Inactivated Campylobacter jejuni antigen (native extract) |
MT-28CJUsl | 灭活的空肠弯曲杆菌抗原(天然提取物) | x100μg | Inactivated Campylobacter jejuni antigen (native extract) |
MT-28SEU | 灭活肠炎沙门氏菌抗原(天然提取物) | x1mg | Inactivated Salmonella enteritidis antigen (native extract) |
MT-28SEUs1 | 灭活肠炎沙门氏菌抗原(天然提取物) | x100μg | Inactivated Salmonella enteritidis antigen (native extract) |
MT-28SPAU | 灭活沙门氏菌副伤寒A抗原(天然提取物) | x1mg | Inactivated Salmonella paratyphi A antigen (native extract) |
MT-28SPAUsl | 灭活沙门氏菌副伤寒A抗原(天然提取物) | x100μg | Inactivated Salmonella paratyphi A antigen (native extract) |
MT-28SPBU | 灭活沙门氏菌副伤寒B抗原(天然提取物) | x1mg | Inactivated Salmonella paratyphi B antigen (native extract) |
MT-28SPBUsl | 灭活沙门氏菌副伤寒B抗原(天然提取物) | x100μg | Inactivated Salmonella paratyphi B antigen (native extract) |
MT-28STMU | 灭活的鼠伤寒沙门氏菌抗原(天然提取物) | x1mg | Inactivated Salmonella typhimurium antigen (native extract) |
MT-28STMUsl | 灭活的鼠伤寒沙门氏菌抗原(天然提取物) | x100μg | Inactivated Salmonella typhimurium antigen (native extract) |
MT-28STU | 灭活伤寒沙门氏菌抗原(天然提取物) | x1mg | Inactivated Salmonella typhi antigen (native extract) |
MT-28STUsl | 灭活伤寒沙门氏菌抗原(天然提取物) | x100μg | Inactivated Salmonella typhi antigen (native extract) |
MT-28LMU | 灭活的单核细胞增生李斯特菌抗原(天然提取物) | x1mg | Inactivated Listeria monocytogenes antigen (native extract) |
MT-28LMUsl | 灭活的单核细胞增生李斯特菌抗原(天然提取物) | x100μg | Inactivated Listeria monocytogenes antigen (native extract) |
MT-28YE3U | 灭活小肠结肠炎耶尔森氏菌O:3抗原(天然提取物) | x1mg | Inactivated Yersinia enterocolitica O:3 antigen (native extract) |
MT-28YE3Usl | 灭活小肠结肠炎耶尔森氏菌O:3抗原(天然提取物) | x100μg | Inactivated Yersinia enterocolitica O:3 antigen (native extract) |
MT-28YE9U | 灭活小肠结肠炎耶尔森氏菌O:9抗原(天然提取物) | x1mg | Inactivated Yersinia enterocolitica O:9 antigen (native extract) |
MT-28YE9Usl | 灭活小肠结肠炎耶尔森氏菌O:9抗原(天然提取物) | x100μg | Inactivated Yersinia enterocolitica O:9 antigen (native extract) |
MT-28SBU | 灭活的鲍氏志贺氏菌抗原(天然提取物) | x1mg | Inactivated Shigella boydii antigen (native extract) |
MT-28SBUsl | 灭活的鲍氏志贺氏菌抗原(天然提取物) | x100μg | Inactivated Shigella boydii antigen (native extract) |
MT-28SDU | 灭活的痢疾志贺氏菌抗原(天然提取物) | x1mg | Inactivated Shigella dysenteriae antigen (native extract) |
MT-28SDUsl | 灭活的痢疾志贺氏菌抗原(天然提取物) | x100μg | Inactivated Shigella dysenteriae antigen (native extract) |
MT-28SFU | 灭活的福氏志贺氏菌抗原(天然提取物) | x1mg | Inactivated Shigella flexneri antigen (native extract) |
MT-28SFUdl | 灭活的福氏志贺氏菌抗原(天然提取物) | x100μg | Inactivated Shigella flexneri antigen (native extract) |
MT-28SSU | 灭活的宋内氏志贺菌抗原(天然提取物) | x1mg | Inactivated Shigella sonnei antigen (native extract) |
MT-28SSUsl | 灭活的宋内氏志贺菌抗原(天然提取物) | x100μg | Inactivated Shigella sonnei antigen (native extract) |
MT-29KOE | 灭活小球隐孢子虫抗原(天然提取物) | x1mg | Inactivated Cryptosporidium parvum antigen (native extract) |
MT-29KOEsl | 灭活小球隐孢子虫抗原(天然提取物) | x100μg | Inactivated Cryptosporidium parvum antigen (native extract) |
MT-29HHB | 人血红蛋白蛋白质(天然提取物) | x1mg | Human Haemoglobin protein (native extract) |
MT-29HHBsl | 人血红蛋白蛋白质(天然提取物) | x100μg | Human Haemoglobin protein (native extract) |
MT-29HLF | 人乳铁蛋白蛋白质(天然提取物) | x1mg | Human Lactoferrin protein (native extract) |
MT-29HLF | 人乳铁蛋白蛋白质(天然提取物) | x100μg | Human Lactoferrin protein (native extract) |
MT-29HTF | 人转铁蛋白蛋白质(天然提取物) | x1mg | Human Transferrin protein (native extract) |
MT-29HTFsl | 人转铁蛋白蛋白质(天然提取物) | x100μg | Human Transferrin protein (native extract) |
MT-20TSS | 溶血性A链球菌抗体 | x1mg | Anti-Strep A Pab |
MT-20TSSsl | 溶血性A链球菌抗体 | x100μg | Anti-Strep A Pab |
MT-18RV3 | 呼吸道合胞病毒单抗(克隆RV3) | x1mg | Anti-RSV Mab (clone RV3) |
MT-18RV3sl | 呼吸道合胞病毒单抗(克隆RV3) | x100μg | Anti-RSV Mab (clone RV3) |
MT-18RV4 | 呼吸道合胞病毒单抗(克隆RV4) | x1mg | Anti-RSV Mab (clone RV4) |
MT-18RV4sl | 呼吸道合胞病毒单抗(克隆RV4) | x100μg | Anti-RSV Mab (clone RV4) |
MT-18A14 | 腺病毒单克隆抗体(克隆A14) | x1mg | Anti-Adenovirus Mab (clone A14) |
MT-18A14sl | 腺病毒单克隆抗体(克隆A14) | x100μg | Anti-Adenovirus Mab (clone A14) |
MT-18A15 | 腺病毒单克隆抗体(克隆A15) | x1mg | Anti-Adenovirus Mab (clone A15) |
MT-18A15Rsl | 腺病毒单克隆抗体(克隆A15) | x100μg | Anti-Adenovirus Mab (clone A15) |
MT-18Y77 | 甲型流感病毒单抗(克隆Y77) | x1mg | Anti-Influenza A Mab (clone Y77) |
MT-18Y77sl | 甲型流感病毒单抗(克隆Y77) | x100μg | Anti-Influenza A Mab (clone Y77) |
MT-18YB91 | 乙型流感病毒单抗(克隆YB91) | x1mg | Anti-Influenza B Mab (clone YB91) |
MT-18YB91sl | 乙型流感病毒单抗(克隆YB91) | x100μg | Anti-Influenza B Mab (clone YB91) |
MT-18LN14 | 嗜肺军团菌单抗(克隆LN14) | x1mg | Anti-Legionella pneumophila Mab (clone LN14) |
MT-18LN14sl | 嗜肺军团菌单抗(克隆LN14) | x100μg | Anti-Legionella pneumophila Mab (clone LN14) |
MT-18LN29 | 嗜肺军团菌单抗(克隆LN29) | x1mg | Anti-Legionella pneumophila Mab (clone LN29) |
MT-18LN29sl | 嗜肺军团菌单抗(克隆LN29) | x100μg | Anti-Legionella pneumophila Mab (clone LN29) |
MT-18SN3 | 肺炎链球菌单克隆抗体(克隆SN3) | x1mg | Anti-Streptococcus pneumoniae Mab (clone SN3) |
MT-18SN3s1 | 肺炎链球菌单克隆抗体(克隆SN3) | x100μg | Anti-Streptococcus pneumoniae Mab (clone SN3) |
MT-18SN4 | 肺炎链球菌单克隆抗体(克隆SN4) | x1mg | Anti-Streptococcus pneumoniae Mab (clone SN4) |
MT-18SN4sl | 肺炎链球菌单克隆抗体(克隆SN4) | x100μg | Anti-Streptococcus pneumoniae Mab (clone SN4) |
MT-25RSV | 呼吸道合胞病毒重组融合蛋白 | x1mg | RSV recombinant fusion protein |
MT-25RSVsl | 呼吸道合胞病毒重组融合蛋白 | x100μg | RSV recombinant fusion protein |
MT-25HEXR | 腺病毒六邻体重组蛋白 | x1mg | Adenovirus HEXON recombinant protein |
MT-25HEXRsl | 腺病毒六邻体重组蛋白 | x100μg | Adenovirus HEXON recombinant protein |
MT-25FAN | 甲型流感病毒重组核蛋白 | x1mg | Influenza A recombinant nucleoprotein |
MT-25FANsl | 甲型流感病毒重组核蛋白 | x100μg | Influenza A recombinant nucleoprotein |
MT-25FBN | 乙型流感病毒重组核蛋白 | x1mg | Influenza B recombinant nucleoprotein |
MT-25FBNsl | 乙型流感病毒重组核蛋白 | x100μg | Influenza B recombinant nucleoprotein |
MT-28SAGU | 灭活A链球菌抗原(天然提取物) | x1mg | Inactivated STREP A antigen (native extract) |
MT-28SAGUsl | 灭活A链球菌抗原(天然提取物) | x100μg | Inactivated STREP A antigen (native extract) |
MT-29RVV | 灭活呼吸道合胞病毒抗原(天然提取物) | x1mg | Inactivated RSV antigen (native extract) |
MT-29RVVsl | 灭活呼吸道合胞病毒抗原(天然提取物) | x100μg | Inactivated RSV antigen (native extract) |
MT-28LNU | 灭活的嗜肺军团菌抗原(天然提取物) | x1mg | Inactivated Legionella pneumophila antigen (native extract) |
MT-28LNUsl | 灭活的嗜肺军团菌抗原(天然提取物) | x100μg | Inactivated Legionella pneumophila antigen (native extract) |
MT-28SPNU | 灭活的肺炎链球菌抗原(天然提取物) | x1mg | Inactivated Streptococcus pneumoniae antigen (native extract) |
MT-28SPNUsl | 灭活的肺炎链球菌抗原(天然提取物) | x100μg | Inactivated Streptococcus pneumoniae antigen (native extract) |
西班牙
3、代谢组学(metabonomics/metabolomics)
定性和定量分析特定条件下的特定生物样品中所有代谢物组分。在分析方法上,样品预处理和检测要满足对所有代谢物组分的检测,因此要保证高灵敏度、高选择性、高通量的要求。庞大的数据结果需要利用化学计量学技术进行数据的解析。
4、代谢指纹分析(metabolic fingerprinting analysis)
高通量定性分析所有的代谢物,以此描述某种生理状态的各种代谢类型的变化。该方法一般不进行定量分析。
生物复杂系统的研究既要求对目标化合物的精确定量分析(靶标分析)又需要对系统整体的定性评价(全局分析),这对分析技术提出了挑战:一方面,现有的面向靶标分析的方法与面向系统的整体分析(全面性)存在矛盾;另一方面,样品的复杂性反过来影响了靶标分析的可靠性(特异性)。
至今为止,还没有一种方法可以真正准确测定所有的代谢物,因此往往将代谢组学不同层次的方法相结合,一方面对于代谢物全谱作全面的分析,另一方面用靶标分析的方法补充全局分析的不足,从而达到分析尽可能多的代谢组分的研究目的。
构建系统进化树的理论方法主要有基于距离的方法UPGMA、ME(Minimum Evolution,zui小进化法)和NJ(Neighbor-Joining,邻接法)等。此外,还包括MP(Maximum parsimony,zui大简约法)、ML(Maximum likelihood,zui大似然法)以及贝叶斯(Bayesian)推断等方法。其中UPGMA法已经较少使用。下面对其中zui常用的3种方法简要介绍。
1、邻接法(Neighbor-Joining,NJ):
该方法通过确定距离zui近或相邻的成对分类单位来使系统树的总距离达到zui小。相邻是指两个分类单位在某一无根分叉树中仅通过一个节点(Node)相连。通过循序地将相邻点合并成新的点,就可以建立一个相应的拓扑树。
2、zui大似然法(Maximum likelihood,ML):
zui早应用于系统发育分析是在对基因频率数据的分析上,后来基于分子序列的分析中也引入了zui大似然法的分析方法。zui大似然法分析中,选取一个特定的替代模型来分析给定的一组序列数据,使得获得的每一个拓扑结构的似然率都为zui大值,然后再挑出其中似然率zui大的拓扑结构作为*树。在zui大似然法的分析中,所考虑的参数并不是拓扑结构而是每个拓扑结构的枝长,并对似然率球zui大值来估计枝长。zui大似然法的建树过程是个很费时的过程,因为在分析过程中有很大的计算量,每个步骤都要考虑内部节点的所有可能性。zui大似然法也是一个比较成熟的参数估计的统计学方法,具有很好的统计学理论基础,在当样本量很大的时候,似然法可以获得参数统计的zui小方差。只要使用了一个合理的、正确的替代模型,zui大似然法可以推导出一个很好的进化树结果。
西班牙
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3, Metabolomics (metabonomics / metabolomics)
Qualitatively and quantitatively analyze all metabolite components in a specific biological sample under specific conditions. In the analytical method, sample preparation and testing to meet the detection of all metabolite components, so to ensure high sensitivity, high selectivity, high throughput requirements. Large data results require the use of chemometrics techniques for data analysis.
4, metabolic fingerprinting analysis (metabolic fingerprinting analysis)
High-throughput qualitative analysis of all metabolites, in order to describe a variety of physiological state of the various metabolic changes. This method is generally not quantitative analysis.
The research of biological complex system not only requires the accurate quantitative analysis (target analysis) but also the qualitative evaluation (global analysis) of the target compound, which poses a challenge to the analytical technique. On the one hand, the existing target-oriented analysis method Contradictory to the overall system-oriented analysis (comprehensiveness); on the other hand, the complexity of the sample in turn affects the reliability (specificity) of the target analysis.
To date, there is no single method for truly accurate determination of all metabolites. Therefore, methods at different levels of metabolomics are often combined to provide a comprehensive analysis of the full spectrum of metabolites on the one hand, and methods of target analysis on the other Complement the deficiencies of global analysis, so as to achieve the purpose of analyzing as many metabolic components as possible.
The theoretical methods of constructing phylogenetic tree mainly include distance-based methods UPGMA, ME (Minimum Evolution) and NJ (Neighbor-Joining). In addition, methods such as MP (Maximum parsimony), ML (Maximum likelihood) and Bayesian inference are also included. Which UPGMA method has been less used. Here's a brief introduction of the three most commonly used methods.
1, Neighbor-Joining (NJ):
The method minimizes the total distance of the system tree by determining the nearest or adjacent pairs of taxa. Adjacent means that two taxa are connected by only one node in a rootless-bifurcated tree. By sequentially merging adjacent points into new points, a corresponding topological tree can be established.
2, Maximum likelihood method (ML):
The earliest application in phylogenetic analysis was based on the analysis of gene frequency data. Later analysis based on molecular sequences also introduced the method of maximum likelihood analysis. In the maximum likelihood analysis, a specific alternative model is selected to analyze a given set of sequence data such that the likelihood of each topology obtained is the maximum, and then the one with the highest likelihood is singled out Structure as the optimal tree. In the analysis of the maximum likelihood method, the parameter under consideration is not the topology but the branch length of each topology, and the branch length is estimated from the maximum value of the likelihood sphere. The process of establishing the maximum likelihood method is a time-consuming process because of the large amount of computation involved in the analysis and each step taking into account all the possibilities of internal nodes. The maximum likelihood method is also a relatively mature statistical method of parameter estimation. It has a good statistical theory foundation. When the sample size is very large, the likelihood method can obtain the minimum variance of the parameter statistics. As long as a reasonable and correct alternative model is used, the maximum likelihood method can derive a good evolutionary tree result.