西班牙Certest腺病毒抗體（克隆A15）
廣州健侖生物科技有限公司
廣州健侖長(zhǎng)期供應(yīng)各種生物原料，主要代理品牌：西班牙Certest。
Certest Biotec，S.L. 是一家獨(dú)立的生物技術(shù)公司，致力于人類臨床領(lǐng)域的IVD診斷產(chǎn)品的開發(fā)和制造。快速檢測(cè)是基于快速、準(zhǔn)確和易于操作的診斷產(chǎn)品。 此外，Cerstest還有多種實(shí)時(shí)PCR產(chǎn)品，可以用于醫(yī)院臨床、實(shí)驗(yàn)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(shù)型公司。公司的發(fā)展是基于新產(chǎn)品的開發(fā)、市場(chǎng)空間和機(jī)遇的探索，十幾年來(lái)一直以高度專業(yè)化，以客戶為導(dǎo)向，不斷得創(chuàng)新，優(yōu)化產(chǎn)品，專業(yè)知識(shí)，取得廣大客戶的信任和支持。Certest的質(zhì)量體系已通過ISO 13485認(rèn)證。
主要產(chǎn)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腺病毒抗體（克隆A15）
我司還提供其它進(jìn)口或國(guó)產(chǎn)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(tuán)菌、化妝品檢測(cè)、食品安全檢測(cè)等試劑盒以及日本生研細(xì)菌分型診斷血清、德國(guó)SiFin診斷血清、丹麥SSI診斷血清等產(chǎn)品。
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西班牙Certest公司簡(jiǎn)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(hào) | 產(chǎn)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(jié)合蛋白單克隆抗體（克隆CP14） | x1mg | Anti-Calprotectin Mab (clone CP14) |
MT-16CP14sl | 鈣結(jié)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(jié)構(gòu)域 | x1mg | Norovirus GI.1 recombinant P domain |
MT-25NGI1sl | 諾如病毒GI.1重組P結(jié)構(gòu)域 | x100μg | Norovirus GI.1 recombinant P domain |
MT-25NGI3 | 諾如病毒GI.3重組P結(jié)構(gòu)域 | x1mg | Norovirus GI.3 recombinant P domain |
MT-25NGI3sl | 諾如病毒GI.3重組P結(jié)構(gòu)域 | x100μg | Norovirus GI.3 recombinant P domain |
MT-25NGII10 | 諾如病毒GII.10重組P結(jié)構(gòu)域 | x1mg | Norovirus GII.10 recombinant P domain |
MT-25NGII10sl | 諾如病毒GII.10重組P結(jié)構(gòu)域 | x100μg | Norovirus GII.10 recombinant P domain |
MT-25NGII17 | 諾如病毒GII.17重組P結(jié)構(gòu)域 | x1mg | Norovirus GII.17 recombinant P domain |
MT-25NGII17sl | 諾如病毒GII.17重組P結(jié)構(gòu)域 | x100μg | Norovirus GII.17 recombinant P domain |
MT-25NGII14 | 諾如病毒GII.4重組P結(jié)構(gòu)域 | x1mg | Norovirus GII.4 recombinant P domain |
MT-25NGII14sl | 諾如病毒GII.4重組P結(jié)構(gòu)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(wú)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(wú)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(wú)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(wú)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(nèi)阿米巴重組蛋白 | x1mg | Entamoeba dispar recombinant protein |
MT-25EDPsl | 內(nèi)阿米巴重組蛋白 | x100μg | Entamoeba dispar recombinant protein |
MT-25EHP | 溶組織內(nèi)阿米巴重組蛋白 | x1mg | Entamoeba histolytica recombinant protein |
MT-25EHPsl | 溶組織內(nèi)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(xì)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(xì)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(jié)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(jié)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(jié)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(jié)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(nèi)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(nèi)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(zhì)（天然提取物） | x1mg | Human Haemoglobin protein (native extract) |
MT-29HHBsl | 人血紅蛋白蛋白質(zhì)（天然提取物） | x100μg | Human Haemoglobin protein (native extract) |
MT-29HLF | 人乳鐵蛋白蛋白質(zhì)（天然提取物） | x1mg | Human Lactoferrin protein (native extract) |
MT-29HLF | 人乳鐵蛋白蛋白質(zhì)（天然提取物） | x100μg | Human Lactoferrin protein (native extract) |
MT-29HTF | 人轉(zhuǎn)鐵蛋白蛋白質(zhì)（天然提取物） | x1mg | Human Transferrin protein (native extract) |
MT-29HTFsl | 人轉(zhuǎn)鐵蛋白蛋白質(zhì)（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(tuán)菌單抗(克隆LN14) | x1mg | Anti-Legionella pneumophila Mab (clone LN14) |
MT-18LN14sl | 嗜肺軍團(tuán)菌單抗(克隆LN14) | x100μg | Anti-Legionella pneumophila Mab (clone LN14) |
MT-18LN29 | 嗜肺軍團(tuán)菌單抗(克隆LN29) | x1mg | Anti-Legionella pneumophila Mab (clone LN29) |
MT-18LN29sl | 嗜肺軍團(tuán)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(yù)鏈球菌抗原（天然提取物） | x1mg | Inactivated STREP A antigen (native extract) |
MT-28SAGUsl | 滅活A(yù)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(tuán)菌抗原（天然提取物） | x1mg | Inactivated Legionella pneumophila antigen (native extract) |
MT-28LNUsl | 滅活的嗜肺軍團(tuán)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) |
西班牙Certest腺病毒抗體（克隆A15）
微生物是地球上種類zui多、數(shù)量zui大、分布zui廣的生物群，與人類、動(dòng)植物和環(huán)境有著密切的相互作用，同時(shí)也是工業(yè)生物技術(shù)的核心及重要的競(jìng)爭(zhēng)戰(zhàn)略資源。隨著測(cè)序技術(shù)的不斷進(jìn)步以及測(cè)序成本的不斷降低，越來(lái)越多的微生物基因組序列得到測(cè)定，其中包括一些重要的病原微生物、工業(yè)微生物、微生物以及生物學(xué)研究中有重要意義的一些模式微生物。
隨著新一代測(cè)序技術(shù)的商業(yè)化應(yīng)用，使得測(cè)序成本不斷降低，測(cè)序通量不斷提高，越來(lái)越多的微生物基因組得到測(cè)定，極大地促進(jìn)了微生物基因組學(xué)的發(fā)展。然而，由于測(cè)序讀長(zhǎng)短、數(shù)據(jù)量大、基因組結(jié)構(gòu)復(fù)雜以及測(cè)序過程中的偏向性等原因，使得已完成測(cè)序的一些物種的基因組中含有數(shù)目不等的空缺區(qū)域。據(jù)統(tǒng)計(jì)，自2008年以來(lái)GenBank釋放的5276個(gè)微生物基因組序列中僅有32% (1692)是完整序列。基因組空缺區(qū)域中可能存在重要的生物學(xué)信息，如果不能補(bǔ)齊所有的Gap，不僅無(wú)法獲得完整的基因組圖譜，還會(huì)給后續(xù)的基因組信息解讀(操縱子結(jié)構(gòu)、基因調(diào)控、SNP分析以及比較基因組等)造成困難。因此，完整微生物基因組序列的獲得需要在完成測(cè)序之后對(duì)空缺區(qū)域進(jìn)行填充，即將測(cè)序拼裝后生成的疊聯(lián)群(Contig)之間的Gap進(jìn)行填充，然后按照一定的次序和方向拼裝生成一條完整的基因組序列(完成圖)，這個(gè)過程稱之為基因組的Gap closure(或補(bǔ)洞)。
Gap closure的關(guān)鍵在于準(zhǔn)確定位不同Contig之間的相對(duì)位置關(guān)系(Linkage關(guān)系)，一旦位置關(guān)系確定，即可通過PCR擴(kuò)增Gap區(qū)域序列或是文庫(kù)克隆步移測(cè)序的方式補(bǔ)齊Gap區(qū)域。然而，由于一些微生物基因組GC含量高、重復(fù)序列數(shù)目多且長(zhǎng)度大(插入序列、rDNA操縱子、大片段重復(fù)等)以及NGS測(cè)序讀長(zhǎng)較短等原因造成測(cè)序偏向性高、拼接后生成過多的Contig，從而增加了Gap closure的難度。此外，缺少基因組參考序列或是與參考序列比對(duì)同源性低等因素，使得生成的Contig無(wú)法有效定位，也會(huì)導(dǎo)致Gap closure難度增加，因此Contig定位被認(rèn)為是微生物基因組Gap closure過程中zui困難和zui耗時(shí)的階段。一些生物信息學(xué)軟件被開發(fā)用于微生物基因組的Gap closure，并取得了一定的效果；但對(duì)于基因組中的高度重復(fù)區(qū)域和低覆蓋率區(qū)域的干擾仍無(wú)法有效解決，必需借助實(shí)驗(yàn)手段獲得額外的序列信息才能zui終完成基因組的Gap closure，因而應(yīng)用的范圍和準(zhǔn)確性受到一定限制。
西班牙
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想了解更多的產(chǎn)品及服務(wù)請(qǐng)掃描下方二維碼：
【公司名稱】 廣州健侖生物科技有限公司
【市場(chǎng)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(hào)二期2幢101-103室
Microbes are the largest, largest and most widely distributed biota in the world. They have close interaction with humans, animals and plants and the environment. They are also the core of industrial biotechnology and an important source of international competitive strategy. As sequencing technology continues to evolve and sequencing costs continue to decline, more and more microbial genome sequences have been determined, including some important pathogenic, industrial, and extreme microorganisms, as well as some models of biological significance in microbiology .
With the commercialization of next-generation sequencing technologies, sequencing costs have been continuously reduced, sequencing fluxes have been continuously increasing, and more and more microorganism genomes have been determined, greatly promoting the development of microbial genomics. However, due to the length of sequencing reads, large amount of data, complicated genome structure and bias in the sequencing process, some species have been sequenced and genomes contain unequal number of vacancies. According to statistics, only 32% (1692) of 5276 microbial genome sequences released by GenBank since 2008 are the complete sequences. There may be important biological information in the genomic locus where not all of the Gap can be populated, not only failing to obtain a complete genome map, but also interpreting subsequent genomic information (operon structure, gene regulation, SNP analysis, and comparative genomics Cause difficulties. Therefore, the complete microbial genome sequence needs to be filled after the completion of the sequencing of the vacancy region, that is to say, the Gap between contigs generated after sequencing and assembly is filled in, and then assembled according to a certain order and direction to generate a complete Genome sequence (complete map), this process is called the genome Gap closure (or fill hole).
The key of Gap closure lies in accuray locating the relative position relationship between different Contigs (Linkage relationship). Once the positional relationship is determined, the Gap region can be filled up by PCR amplification of Gap region sequence or library clone walking sequencing. However, due to the high sequencing accuracy of some GCs such as high GC content, large number of repetitive sequences and large length (insert sequence, rDNA operator, large fragment repeat, etc.) and NGS sequencing, Contig, which increases the difficulty of Gap closure. In addition, the absence of genomic reference sequences or the lack of homology to reference sequences make Contig unable to be efficiently mapped and result in increased difficulty of Gap closure, so Contig localization is considered to be the most difficult in the Gap closure of microbial genomes And the most time-consuming stage. Some bioinformatics software has been developed for use in the Gap closure of microbial genomes and has achieved some results. However, the interference with highly repeated regions and low coverage regions in the genome can not be effectively solved, and additional sequences must be obtained experimentally Information can eventually complete the genome Gap closure, and thus the scope and accuracy of the application subject to certain restrictions.
