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西班牙Certest星状病毒衣壳重组蛋白
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星状病毒衣壳重组蛋白
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Certest星状病毒衣壳重组蛋白
邻接法（Neighbor Joining，NJ）是距离法建树中比较有实用价值的方法。与UPGMA相比，NJ方法不用假设进化树中所有物种的进化速率相同，因此在大多数情况下比较令人信服。该方法思想是：通过确定距离zui近的成对分类物种组来使进化树的进化距离之和达到zui小。在进行序列合并时，不仅要满足待合并序列进化距离的相近，同时也要求待合并的序列与其它序列的近似距离较远。
zui大似然法（Maximum likelihood，ML）于1981年被提出，该方法构建思想基于统计学。在预先选择的进化模型下计算每一种进化树生成的可能性，选择zui大可能性的进化树即为zui大似然树。zui大似然法在构建进化树的准确度方面很高，但是在处理大数据量时效率比较低，并且对模型的依赖比较严重。
zui大简约法（Maximum parsimony，MP）依据各个位置上由一条生物序列突变成另一条生物序列所需zui小数量突变来进行比较分析和聚类树生成，zui终的进化树是基于整条序列所需的突变总数的。
高精度宏基因组特指具有明确科学或技术问题导向的宏基因组研究，能够极大降低传统宏基因组的复杂度，显著提高其科学研究与应用开发价值。例如，每克土壤中基因数量zui高可达4万亿，目前条件下很难整体破译所有功能基因，特别是数量少，但功能重要的基因。因此，通过对复杂环境样品进行特定处理，如针对病原微生物滤膜处理，针对互营菌的共生培养以及免培养策略等，即可定向培育目标微生物群落，开展高精度宏基因组分析挖掘。
宏基因组及海量数据分析是生物信息学和相关学科未来重要的前沿技术。例如，在环境科学研究中，每克土壤通常含有10亿微生物，每个微生物平均有4000个基因，宏基因组即可针对每克土壤中的这4万亿个基因进行分类、注释，并挖掘其功能。但是，据估计，用目前的技术对环境中有高达99%的微生物还难以进行分离或培养，对这些微生物的功能及其基因序列更是一无所知。在没有参考序列的条件下，如何对某种环境下海量的微生物遗传信息进行储存、分类和比较分析，是目前宏基因组研究所遇到的难点之一。
宏基因组的快速注释用子系统技术（Metagenomic for Rapid Annotations using Subsystems Technology，MG-RAST）能有效解决这一问题，该技术特别适用于一些非生物信息专业实验室，极大促进了宏基因组的科学研究与技术应用。
西班牙Certest星状病毒衣壳重组蛋白
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【公司名称】 广州健仑生物科技有限公司
【市场部】 杨永汉
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【腾讯 】 2042552662
【公司地址】 广州清华科技园创新基地番禺石楼镇创启路63号二期2幢101-103室
Neighbor Joining (NJ) is a more practical method of establishing distance. In contrast to UPGMA, the NJ method does not assume that all species in the phylogenetic tree will evolve at the same rate and is therefore most convincing in most cases. The idea of this method is to minimize the sum of the evolutionary distances of the evolutionary trees by identifying the nearest pairwise species groups. When performing sequence merging, not only the evolutionary distances of the sequences to be merged are similar, but also the distances between the sequences to be merged and the approximate distances of other sequences are also required.
The Maximum Likelihood (ML) was proposed in 1981, and the idea of this method is based on statistics. In the pre-selected evolutionary model to calculate the possibility of each generation of evolutionary tree, choose the maximum likelihood of the tree is the maximum likelihood tree. Maximum likelihood method in building the accuracy of the tree is very high, but when dealing with large amounts of data, the efficiency is low, and more dependent on the model.
Maximum parsimony (MP) performs comparative analysis and clustering tree generation based on the minimum number of mutations needed to mutate one biological sequence to another at each position. The final phylogenetic tree is based on the entire sequence required The total number of mutations.
High-precision metagenomics specifically refers to metagenomic research with clear scientific or technical problems, which can greatly reduce the complexity of the traditional metagenome and significantly increase the value of its scientific research and application development. For example, the maximum number of genes per gram of soil is up to 4 trillion, making it difficult to decipher all functional genes as a whole in the current conditions, especially for a small number of genes that are functionally important. Therefore, targeted processing of complex environmental samples, such as the treatment of pathogenic microorganisms, co-culture of intercropped bacteria, and culture-free strategies, targeted c*tion of targeted microorganisms and mining of metagenomics with high precision.
Metagenomics and mass data analysis are important cutting-edge technologies for bioinformatics and related disciplines in the future. For example, in environmental sciences, where soil contains typically 1 billion microorganisms per gram of soil and an average of 4,000 genes per microorganism, the metagenome can classify, annotate and interpret these 4 trillion genes per gram of soil Features. However, it is estimated that up to 99% of the microorganisms in the environment can hardly be isolated or cultured using the current technology, even without any knowledge of the function of these microorganisms and their genetic sequences. Under the condition of no reference sequence, how to store, sort and comparatively analyze the genetic information of a large number of microorganisms in an environment is one of the difficulties encountered in the metagenomics research.
This problem can be effectively solved by Metagenomic for Rapid Annotations using Subsystems Technology (MG-RAST), which is especially suitable for some non-biological information laboratories and greatly promotes the science of metagenomics Research and Technology Application.
