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西班牙Certest星狀病毒衣殼重組蛋白
廣州健侖生物科技有限公司
廣州健侖長期供應各種生物原料,主要代理品牌:西班牙Certest。
Certest Biotec,S.L. 是一家獨立的生物技術公司,致力于人類臨床領域的IVD診斷產品的開發(fā)和制造??焖贆z測是基于快速、準確和易于操作的診斷產品。 此外,Cerstest還有多種實時PCR產品,可以用于醫(yī)院臨床、實驗室科研等。
Certest公司于2002年在薩拉戈薩成立,是一家創(chuàng)新技術型公司。公司的發(fā)展是基于新產品的開發(fā)、市場空間和機遇的探索,十幾年來一直以高度專業(yè)化,以客戶為導向,不斷得創(chuàng)新,優(yōu)化產品,專業(yè)知識,取得廣大客戶的信任和支持。Certest的質量體系已通過ISO 13485認證。
主要產品包括各種生物單克隆抗原抗體、重組蛋白。
輪狀病毒單克隆抗體、腺病毒抗體、星狀病毒單克隆抗體、諾如病毒單克隆抗體、幽門螺旋桿菌抗體、隱球菌抗體、腸道病毒抗體、賈第鞭毛蟲抗體、彎曲桿菌抗體、阿米巴原蟲抗體、呼吸道合胞病毒單抗等等。
西班牙Certest星狀病毒衣殼重組蛋白
我司還提供其它進口或國產試劑盒:登革熱、瘧疾、流感、A鏈球菌、合胞病毒、腮病毒、乙腦、寨卡、黃熱病、基孔肯雅熱、克錐蟲病、違禁品濫用、肺炎球菌、軍團菌、化妝品檢測、食品安全檢測等試劑盒以及日本生研細菌分型診斷血清、德國SiFin診斷血清、丹麥SSI診斷血清等產品。
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西班牙Certest公司簡介
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】
貨號 | 產品名稱 | 規(guī)格 | 英文名稱 |
MT-16R15 | 輪狀病毒單克隆抗體(克隆R15) | x1mg | Anti-Rotavirus Mab (clone R15) |
MT-16R15s1 | 輪狀病毒單克隆抗體(克隆R15) | x100μg | Anti-Rotavirus Mab (clone R15) |
MT-18A15 | 腺病毒抗體(克隆A15) | x1mg | Anti-Adenovirus Mab (clone A15) |
MT-18A15s1 | 腺病毒抗體(克隆A15) | x100μg | Anti-Adenovirus Mab (clone A15) |
MT-18AT18 | 星狀病毒單克隆抗體(克隆AT18) | x1mg | Anti-Astrovirus Mab (clone AT18) |
MT-18AT18s1 | 星狀病毒單克隆抗體(克隆AT18) | x100μg | Anti-Astrovirus Mab (clone AT18) |
MT-18AT8 | 星狀病毒單克隆抗體(克隆AT8) | x1mg | Anti-Astrovirus Mab (clone AT8) |
MT-18AT8s1 | 星狀病毒單克隆抗體(克隆AT8) | x100μg | Anti-Astrovirus Mab (clone AT8) |
MT-18NG28 | 諾如病毒GI單克隆抗體(克隆NG28) | x1mg | Anti-Norovirus GI Mab (clone NG28) |
MT-18NG28sl | 諾如病毒GI單克隆抗體(克隆NG28) | x100μg | Anti-Norovirus GI Mab (clone NG28) |
MT-18NP8 | 諾如病毒GII單克隆抗體(克隆NP8) | x1mg | Anti-Norovirus GII Mab (clone NP8) |
MT-18NP8sl | 諾如病毒GII單克隆抗體(克隆NP8) | x100μg | Anti-Norovirus GII Mab (clone NP8) |
MT-18EV5 | 腸道病毒抗體(克隆EV5) | x1mg | Anti-Enterovirus Mab (clone EV5) |
MT-18EV5sl | 腸道病毒抗體(克隆EV5) | x100μg | Anti-Enterovirus Mab (clone EV5) |
MT-16P2 | 幽門螺旋桿菌抗體(克隆P2)HP抗體 | x1mg | Anti-H. pylori Mab (clone P2) |
MT-16P2sl | 幽門螺旋桿菌抗體(克隆P2)HP抗體 | x100μg | Anti-H. pylori Mab (clone P2) |
MT-16GD10 | 艱難梭菌抗體(克隆GD10) | x1mg | Anti-GDH Mab (clone GD10) |
MT-16GD10sl | 艱難梭菌抗體(克隆GD10) | x100μg | Anti-GDH Mab (clone GD10) |
MT-18TA5 | 艱難梭菌毒素A抗(克隆TA5) | x1mg | Anti-CD Toxin A Mab (clone TA5) |
MT-18TA5sl | 艱難梭菌毒素A抗(克隆TA5) | x100μg | Anti-CD Toxin A Mab (clone TA5) |
MT-18TA7 | 艱難梭菌毒素A抗(克隆TA7) | x1mg | Anti-CD Toxin A Mab (clone TA7) |
MT-18TA7sl | 艱難梭菌毒素A抗(克隆TA7) | x100μg | Anti-CD Toxin A Mab (clone TA7) |
MT-18TB41 | 艱難梭菌毒素B抗(克隆TB41) | x1mg | Anti-CD Toxin B Mab (clone TB41) |
MT-18TB41sl | 艱難梭菌毒素B抗(克隆TB41) | x100μg | Anti-CD Toxin B Mab (clone TB41) |
MT-18TB48 | 艱難梭菌毒素B抗(克隆TB48) | x1mg | Anti-CD Toxin B Mab (clone TB48) |
MT-18TB48sl | 艱難梭菌毒素B抗(克隆TB48) | x100μg | Anti-CD Toxin B Mab (clone TB48) |
MT-18E10 | 大腸桿菌O157抗體(克隆E10) | x1mg | Anti-E. coli O157 Mab (clone E10) |
MT-18E10sl | 大腸桿菌O157抗體(克隆E10) | x100μg | Anti-E. coli O157 Mab (clone E10) |
MT-16CA29 | 彎曲桿菌抗體(克隆ECA29) | x1mg | Anti-Campylobacter Mab (clone CA29) |
MT-16CA29sl | 彎曲桿菌抗體(克隆ECA29) | x100μg | Anti-Campylobacter Mab (clone CA29) |
MT-18K31 | 隱球菌抗體(克隆K31) | x1mg | Anti-Crypto Mab (clone K31) |
MT-18K31sl | 隱球菌抗體(克隆K31) | x100μg | Anti-Crypto Mab (clone K31) |
MT-16G18 | 賈第鞭毛蟲抗體(克隆G18) | x1mg | Anti-Giardia Mab trophozoite protein (clone G18) |
MT-16G18sl | 賈第鞭毛蟲抗體(克隆G18) | x100μg | Anti-Giardia Mab trophozoite protein (clone G18) |
MT-16G22 | 賈第鞭毛蟲抗體(克隆G22) | x1mg | Anti-Giardia Mab trophozoite protein (clone G22) |
MT-16G22sl | 賈第鞭毛蟲抗體(克隆G22) | x100μg | Anti-Giardia Mab trophozoite protein (clone G22) |
MT-18EH30 | 阿米巴原蟲抗體(克隆H30) | x1mg | Anti-Entamoeba Mab (clone EH30) |
MT-18EH30sl | 阿米巴原蟲抗體(克隆H30) | x100μg | Anti-Entamoeba Mab (clone EH30) |
MT-16CP14 | 鈣結合蛋白單克隆抗體(克隆CP14) | x1mg | Anti-Calprotectin Mab (clone CP14) |
MT-16CP14sl | 鈣結合蛋白單克隆抗體(克隆CP14) | x100μg | Anti-Calprotectin Mab (clone CP14) |
MT-16F22 | 血紅蛋白單抗(克隆F22) | x1mg | Anti-Haemoglobin Mab (clone F22) |
MT-16F22sl | 血紅蛋白單抗(克隆F22) | x100μg | Anti-Haemoglobin Mab (clone F22) |
MT-16LC16 | 乳鐵蛋白單抗(克隆LC16) | x1mg | Anti-Lactoferrin Mab (clone LC16) |
MT-16LC16sl | 乳鐵蛋白單抗(克隆LC16) | x100μg | Anti-Lactoferrin Mab (clone LC16) |
MT-16LC4 | 乳鐵蛋白單抗(克隆LC4) | x1mg | Anti-Lactoferrin Mab (clone LC4) |
MT-16LC4sl | 乳鐵蛋白單抗(克隆LC4) | x100μg | Anti-Lactoferrin Mab (clone LC4) |
MT-26VP6 | 輪狀病毒VP6重組蛋白 | x1mg | Rotavirus VP6 recombinant protein |
MT-26VP6 | 輪狀病毒VP6重組蛋白 | x100μg | Rotavirus VP6 recombinant protein |
MT-25HEX | 腺病毒HEXON重組蛋白 | x1mg | Adenovirus HEXON recombinant protein |
MT-25HEXsl | 腺病毒HEXON重組蛋白 | x100μg | Adenovirus HEXON recombinant protein |
MT-25AST | 星狀病毒衣殼重組蛋白 | x1mg | Astrovirus capsid recombinant protein |
MT-25ASTsl | 星狀病毒衣殼重組蛋白 | x100μg | Astrovirus capsid recombinant protein |
MT-25NGI1 | 諾如病毒GI.1重組P結構域 | x1mg | Norovirus GI.1 recombinant P domain |
MT-25NGI1sl | 諾如病毒GI.1重組P結構域 | x100μg | Norovirus GI.1 recombinant P domain |
MT-25NGI3 | 諾如病毒GI.3重組P結構域 | x1mg | Norovirus GI.3 recombinant P domain |
MT-25NGI3sl | 諾如病毒GI.3重組P結構域 | x100μg | Norovirus GI.3 recombinant P domain |
MT-25NGII10 | 諾如病毒GII.10重組P結構域 | x1mg | Norovirus GII.10 recombinant P domain |
MT-25NGII10sl | 諾如病毒GII.10重組P結構域 | x100μg | Norovirus GII.10 recombinant P domain |
MT-25NGII17 | 諾如病毒GII.17重組P結構域 | x1mg | Norovirus GII.17 recombinant P domain |
MT-25NGII17sl | 諾如病毒GII.17重組P結構域 | x100μg | Norovirus GII.17 recombinant P domain |
MT-25NGII14 | 諾如病毒GII.4重組P結構域 | x1mg | Norovirus GII.4 recombinant P domain |
MT-25NGII14sl | 諾如病毒GII.4重組P結構域 | x100μg | Norovirus GII.4 recombinant P domain |
MT-25ETV | 腸道病毒VP1重組蛋白 | x1mg | Enterovirus VP1 recombinant protein |
MT-25ETVs1 | 腸道病毒VP1重組蛋白 | x100μg | Enterovirus VP1 recombinant protein |
MT-25PCH | 幽門螺桿菌重組外膜蛋白 | x1mg | H. pylori recombinant outer membrane protein |
MT-25PCHs1 | 幽門螺桿菌重組外膜蛋白 | x100μg | H. pylori recombinant outer membrane protein |
MT-25GDH | 艱難梭菌GDH重組蛋白 | x1mg | Clostridium difficile GDH recombinant protein |
MT-25GDHsl | 艱難梭菌GDH重組蛋白 | x100μg | Clostridium difficile GDH recombinant protein |
MT-24TXA | 艱難梭菌毒素A重組蛋白(無毒性片段) | x1mg | C. difficile Toxin A recombinant protein (fragment without toxic activity) |
MT-24TXAsl | 艱難梭菌毒素A重組蛋白(無毒性片段) | x100μg | C. difficile Toxin A recombinant protein (fragment without toxic activity) |
MT-24TXB | 艱難梭菌毒素B重組蛋白(無毒性片段) | x1mg | C. difficile Toxin B recombinant protein (fragment without toxic activity) |
MT-24TXBsl | 艱難梭菌毒素B重組蛋白(無毒性片段) | x100μg | C. difficile Toxin B recombinant protein (fragment without toxic activity) |
MT-25STX | 大腸桿菌O157 VT1重組蛋白 | x1mg | E. coli O157 VT1 recombinant protein |
MT-25STXsl | 大腸桿菌O157 VT1重組蛋白 | x100μg | E. coli O157 VT1 recombinant protein |
MT-25VT2 | 大腸桿菌O157 VT2重組蛋白 | x1mg | E. coli O157 VT2 recombinant protein |
MT-25VT2sl | 大腸桿菌O157 VT2重組蛋白 | x100μg | E. coli O157 VT2 recombinant protein |
MT-25CCP | 彎曲桿菌重組外膜蛋白 | x1mg | Campylobacter coli recombinant outer membrane protein |
MT-25CCPsl | 彎曲桿菌重組外膜蛋白 | x100μg | Campylobacter coli recombinant outer membrane protein |
MT-25CEP | 空腸彎曲桿菌重組外膜蛋白 | x1mg | Campylobacter jejuni recombinant outer membrane protein |
MT-25CEPsl | 空腸彎曲桿菌重組外膜蛋白 | x100μg | Campylobacter jejuni recombinant outer membrane protein |
MT-25A1G | 賈第蟲腸道滋養(yǎng)體重組蛋白 | x1mg | Giardia intestinalis trophozoite recombinant protein |
MT-25A1Gsl | 賈第蟲腸道滋養(yǎng)體重組蛋白 | x100μg | Giardia intestinalis trophozoite recombinant protein |
MT-25GCP | 賈第蟲腸囊菌重組蛋白 | x1mg | Giardia intestinalis cyst recombinant protein |
MT-25GCPsl | 賈第蟲腸囊菌重組蛋白 | x100μg | Giardia intestinalis cyst recombinant protein |
MT-25EDP | 內阿米巴重組蛋白 | x1mg | Entamoeba dispar recombinant protein |
MT-25EDPsl | 內阿米巴重組蛋白 | x100μg | Entamoeba dispar recombinant protein |
MT-25EHP | 溶組織內阿米巴重組蛋白 | x1mg | Entamoeba histolytica recombinant protein |
MT-25EHPsl | 溶組織內阿米巴重組蛋白 | x100μg | Entamoeba histolytica recombinant protein |
MT-25HCP | 人類鈣衛(wèi)蛋白重組蛋白 | x1mg | Human Calprotectin recombinant protein |
MT-25HCPs1 | 人類鈣衛(wèi)蛋白重組蛋白 | x100μg | Human Calprotectin recombinant protein |
MT-31NGA | 諾如病毒GI.1重組VLP | x1mg | Norovirus GI.1 recombinant VLP |
MT-31NGAsl | 諾如病毒GI.1重組VLP | x100μg | Norovirus GI.1 recombinant VLP |
MT-31NPA | 諾如病毒GII.4重組VLP | x1mg | Norovirus GII.4 recombinant VLP |
MT-31NPAsl | 諾如病毒GII.4重組VLP | x100μg | Norovirus GII.4 recombinant VLP |
MT-28PECU | 滅活的幽門螺桿菌抗原(天然提取物) | x1mg | Inactivated H. pylori antigen (native extract) |
MT-28PECUsl | 滅活的幽門螺桿菌抗原(天然提取物) | x100μg | Inactivated H. pylori antigen (native extract) |
MT-28EC7U | 滅活的大腸桿菌O157抗原(天然提取物) | x1mg | Inactivated E. coli O157 antigen (native extract) |
MT-28EC7Usl | 滅活的大腸桿菌O157抗原(天然提取物) | x100μg | Inactivated E. coli O157 antigen (native extract) |
MT-28CCU | 滅活的大腸桿菌抗原(天然提取物) | x1mg | Inactivated Campylobacter coli antigen (native extract) |
MT-28CCUsl | 滅活的大腸桿菌抗原(天然提取物) | x100μg | Inactivated Campylobacter coli antigen (native extract) |
MT-28CJU | 滅活的空腸彎曲桿菌抗原(天然提取物) | x1mg | Inactivated Campylobacter jejuni antigen (native extract) |
MT-28CJUsl | 滅活的空腸彎曲桿菌抗原(天然提取物) | x100μg | Inactivated Campylobacter jejuni antigen (native extract) |
MT-28SEU | 滅活腸炎沙門氏菌抗原(天然提取物) | x1mg | Inactivated Salmonella enteritidis antigen (native extract) |
MT-28SEUs1 | 滅活腸炎沙門氏菌抗原(天然提取物) | x100μg | Inactivated Salmonella enteritidis antigen (native extract) |
MT-28SPAU | 滅活沙門氏菌副傷寒A抗原(天然提取物) | x1mg | Inactivated Salmonella paratyphi A antigen (native extract) |
MT-28SPAUsl | 滅活沙門氏菌副傷寒A抗原(天然提取物) | x100μg | Inactivated Salmonella paratyphi A antigen (native extract) |
MT-28SPBU | 滅活沙門氏菌副傷寒B抗原(天然提取物) | x1mg | Inactivated Salmonella paratyphi B antigen (native extract) |
MT-28SPBUsl | 滅活沙門氏菌副傷寒B抗原(天然提取物) | x100μg | Inactivated Salmonella paratyphi B antigen (native extract) |
MT-28STMU | 滅活的鼠傷寒沙門氏菌抗原(天然提取物) | x1mg | Inactivated Salmonella typhimurium antigen (native extract) |
MT-28STMUsl | 滅活的鼠傷寒沙門氏菌抗原(天然提取物) | x100μg | Inactivated Salmonella typhimurium antigen (native extract) |
MT-28STU | 滅活傷寒沙門氏菌抗原(天然提取物) | x1mg | Inactivated Salmonella typhi antigen (native extract) |
MT-28STUsl | 滅活傷寒沙門氏菌抗原(天然提取物) | x100μg | Inactivated Salmonella typhi antigen (native extract) |
MT-28LMU | 滅活的單核細胞增生李斯特菌抗原(天然提取物) | x1mg | Inactivated Listeria monocytogenes antigen (native extract) |
MT-28LMUsl | 滅活的單核細胞增生李斯特菌抗原(天然提取物) | x100μg | Inactivated Listeria monocytogenes antigen (native extract) |
MT-28YE3U | 滅活小腸結腸炎耶爾森氏菌O:3抗原(天然提取物) | x1mg | Inactivated Yersinia enterocolitica O:3 antigen (native extract) |
MT-28YE3Usl | 滅活小腸結腸炎耶爾森氏菌O:3抗原(天然提取物) | x100μg | Inactivated Yersinia enterocolitica O:3 antigen (native extract) |
MT-28YE9U | 滅活小腸結腸炎耶爾森氏菌O:9抗原(天然提取物) | x1mg | Inactivated Yersinia enterocolitica O:9 antigen (native extract) |
MT-28YE9Usl | 滅活小腸結腸炎耶爾森氏菌O:9抗原(天然提取物) | x100μg | Inactivated Yersinia enterocolitica O:9 antigen (native extract) |
MT-28SBU | 滅活的鮑氏志賀氏菌抗原(天然提取物) | x1mg | Inactivated Shigella boydii antigen (native extract) |
MT-28SBUsl | 滅活的鮑氏志賀氏菌抗原(天然提取物) | x100μg | Inactivated Shigella boydii antigen (native extract) |
MT-28SDU | 滅活的痢疾志賀氏菌抗原(天然提取物) | x1mg | Inactivated Shigella dysenteriae antigen (native extract) |
MT-28SDUsl | 滅活的痢疾志賀氏菌抗原(天然提取物) | x100μg | Inactivated Shigella dysenteriae antigen (native extract) |
MT-28SFU | 滅活的福氏志賀氏菌抗原(天然提取物) | x1mg | Inactivated Shigella flexneri antigen (native extract) |
MT-28SFUdl | 滅活的福氏志賀氏菌抗原(天然提取物) | x100μg | Inactivated Shigella flexneri antigen (native extract) |
MT-28SSU | 滅活的宋內氏志賀菌抗原(天然提取物) | x1mg | Inactivated Shigella sonnei antigen (native extract) |
MT-28SSUsl | 滅活的宋內氏志賀菌抗原(天然提取物) | x100μg | Inactivated Shigella sonnei antigen (native extract) |
MT-29KOE | 滅活小球隱孢子蟲抗原(天然提取物) | x1mg | Inactivated Cryptosporidium parvum antigen (native extract) |
MT-29KOEsl | 滅活小球隱孢子蟲抗原(天然提取物) | x100μg | Inactivated Cryptosporidium parvum antigen (native extract) |
MT-29HHB | 人血紅蛋白蛋白質(天然提取物) | x1mg | Human Haemoglobin protein (native extract) |
MT-29HHBsl | 人血紅蛋白蛋白質(天然提取物) | x100μg | Human Haemoglobin protein (native extract) |
MT-29HLF | 人乳鐵蛋白蛋白質(天然提取物) | x1mg | Human Lactoferrin protein (native extract) |
MT-29HLF | 人乳鐵蛋白蛋白質(天然提取物) | x100μg | Human Lactoferrin protein (native extract) |
MT-29HTF | 人轉鐵蛋白蛋白質(天然提取物) | x1mg | Human Transferrin protein (native extract) |
MT-29HTFsl | 人轉鐵蛋白蛋白質(天然提取物) | x100μg | Human Transferrin protein (native extract) |
MT-20TSS | 溶血性A鏈球菌抗體 | x1mg | Anti-Strep A Pab |
MT-20TSSsl | 溶血性A鏈球菌抗體 | x100μg | Anti-Strep A Pab |
MT-18RV3 | 呼吸道合胞病毒單抗(克隆RV3) | x1mg | Anti-RSV Mab (clone RV3) |
MT-18RV3sl | 呼吸道合胞病毒單抗(克隆RV3) | x100μg | Anti-RSV Mab (clone RV3) |
MT-18RV4 | 呼吸道合胞病毒單抗(克隆RV4) | x1mg | Anti-RSV Mab (clone RV4) |
MT-18RV4sl | 呼吸道合胞病毒單抗(克隆RV4) | x100μg | Anti-RSV Mab (clone RV4) |
MT-18A14 | 腺病毒單克隆抗體(克隆A14) | x1mg | Anti-Adenovirus Mab (clone A14) |
MT-18A14sl | 腺病毒單克隆抗體(克隆A14) | x100μg | Anti-Adenovirus Mab (clone A14) |
MT-18A15 | 腺病毒單克隆抗體(克隆A15) | x1mg | Anti-Adenovirus Mab (clone A15) |
MT-18A15Rsl | 腺病毒單克隆抗體(克隆A15) | x100μg | Anti-Adenovirus Mab (clone A15) |
MT-18Y77 | 甲型流感病毒單抗(克隆Y77) | x1mg | Anti-Influenza A Mab (clone Y77) |
MT-18Y77sl | 甲型流感病毒單抗(克隆Y77) | x100μg | Anti-Influenza A Mab (clone Y77) |
MT-18YB91 | 乙型流感病毒單抗(克隆YB91) | x1mg | Anti-Influenza B Mab (clone YB91) |
MT-18YB91sl | 乙型流感病毒單抗(克隆YB91) | x100μg | Anti-Influenza B Mab (clone YB91) |
MT-18LN14 | 嗜肺軍團菌單抗(克隆LN14) | x1mg | Anti-Legionella pneumophila Mab (clone LN14) |
MT-18LN14sl | 嗜肺軍團菌單抗(克隆LN14) | x100μg | Anti-Legionella pneumophila Mab (clone LN14) |
MT-18LN29 | 嗜肺軍團菌單抗(克隆LN29) | x1mg | Anti-Legionella pneumophila Mab (clone LN29) |
MT-18LN29sl | 嗜肺軍團菌單抗(克隆LN29) | x100μg | Anti-Legionella pneumophila Mab (clone LN29) |
MT-18SN3 | 肺炎鏈球菌單克隆抗體(克隆SN3) | x1mg | Anti-Streptococcus pneumoniae Mab (clone SN3) |
MT-18SN3s1 | 肺炎鏈球菌單克隆抗體(克隆SN3) | x100μg | Anti-Streptococcus pneumoniae Mab (clone SN3) |
MT-18SN4 | 肺炎鏈球菌單克隆抗體(克隆SN4) | x1mg | Anti-Streptococcus pneumoniae Mab (clone SN4) |
MT-18SN4sl | 肺炎鏈球菌單克隆抗體(克隆SN4) | x100μg | Anti-Streptococcus pneumoniae Mab (clone SN4) |
MT-25RSV | 呼吸道合胞病毒重組融合蛋白 | x1mg | RSV recombinant fusion protein |
MT-25RSVsl | 呼吸道合胞病毒重組融合蛋白 | x100μg | RSV recombinant fusion protein |
MT-25HEXR | 腺病毒六鄰體重組蛋白 | x1mg | Adenovirus HEXON recombinant protein |
MT-25HEXRsl | 腺病毒六鄰體重組蛋白 | x100μg | Adenovirus HEXON recombinant protein |
MT-25FAN | 甲型流感病毒重組核蛋白 | x1mg | Influenza A recombinant nucleoprotein |
MT-25FANsl | 甲型流感病毒重組核蛋白 | x100μg | Influenza A recombinant nucleoprotein |
MT-25FBN | 乙型流感病毒重組核蛋白 | x1mg | Influenza B recombinant nucleoprotein |
MT-25FBNsl | 乙型流感病毒重組核蛋白 | x100μg | Influenza B recombinant nucleoprotein |
MT-28SAGU | 滅活A鏈球菌抗原(天然提取物) | x1mg | Inactivated STREP A antigen (native extract) |
MT-28SAGUsl | 滅活A鏈球菌抗原(天然提取物) | x100μg | Inactivated STREP A antigen (native extract) |
MT-29RVV | 滅活呼吸道合胞病毒抗原(天然提取物) | x1mg | Inactivated RSV antigen (native extract) |
MT-29RVVsl | 滅活呼吸道合胞病毒抗原(天然提取物) | x100μg | Inactivated RSV antigen (native extract) |
MT-28LNU | 滅活的嗜肺軍團菌抗原(天然提取物) | x1mg | Inactivated Legionella pneumophila antigen (native extract) |
MT-28LNUsl | 滅活的嗜肺軍團菌抗原(天然提取物) | x100μg | Inactivated Legionella pneumophila antigen (native extract) |
MT-28SPNU | 滅活的肺炎鏈球菌抗原(天然提取物) | x1mg | Inactivated Streptococcus pneumoniae antigen (native extract) |
MT-28SPNUsl | 滅活的肺炎鏈球菌抗原(天然提取物) | x100μg | Inactivated Streptococcus pneumoniae antigen (native extract) |
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鄰接法(Neighbor Joining,NJ)是距離法建樹中比較有實用價值的方法。與UPGMA相比,NJ方法不用假設進化樹中所有物種的進化速率相同,因此在大多數情況下比較令人信服。該方法思想是:通過確定距離zui近的成對分類物種組來使進化樹的進化距離之和達到zui小。在進行序列合并時,不僅要滿足待合并序列進化距離的相近,同時也要求待合并的序列與其它序列的近似距離較遠。
zui大似然法(Maximum likelihood,ML)于1981年被提出,該方法構建思想基于統計學。在預先選擇的進化模型下計算每一種進化樹生成的可能性,選擇zui大可能性的進化樹即為zui大似然樹。zui大似然法在構建進化樹的準確度方面很高,但是在處理大數據量時效率比較低,并且對模型的依賴比較嚴重。
zui大簡約法(Maximum parsimony,MP)依據各個位置上由一條生物序列突變成另一條生物序列所需zui小數量突變來進行比較分析和聚類樹生成,zui終的進化樹是基于整條序列所需的突變總數的。
高精度宏基因組特指具有明確科學或技術問題導向的宏基因組研究,能夠極大降低傳統宏基因組的復雜度,顯著提高其科學研究與應用開發(fā)價值。例如,每克土壤中基因數量zui高可達4萬億,目前條件下很難整體破譯所有功能基因,特別是數量少,但功能重要的基因。因此,通過對復雜環(huán)境樣品進行特定處理,如針對病原微生物濾膜處理,針對互營菌的共生培養(yǎng)以及免培養(yǎng)策略等,即可定向培育目標微生物群落,開展高精度宏基因組分析挖掘。
宏基因組及海量數據分析是生物信息學和相關學科未來重要的前沿技術。例如,在環(huán)境科學研究中,每克土壤通常含有10億微生物,每個微生物平均有4000個基因,宏基因組即可針對每克土壤中的這4萬億個基因進行分類、注釋,并挖掘其功能。但是,據估計,用目前的技術對環(huán)境中有高達99%的微生物還難以進行分離或培養(yǎng),對這些微生物的功能及其基因序列更是一無所知。在沒有參考序列的條件下,如何對某種環(huán)境下海量的微生物遺傳信息進行儲存、分類和比較分析,是目前宏基因組研究所遇到的難點之一。
宏基因組的快速注釋用子系統技術(Metagenomic for Rapid Annotations using Subsystems Technology,MG-RAST)能有效解決這一問題,該技術特別適用于一些非生物信息專業(yè)實驗室,極大促進了宏基因組的科學研究與技術應用。
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【公司名稱】 廣州健侖生物科技有限公司
【市場部】 楊永漢
【】
【騰訊 】 2042552662
【公司地址】 廣州清華科技園創(chuàng)新基地番禺石樓鎮(zhèn)創(chuàng)啟路63號二期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.
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