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西班牙Certest滅活的空腸彎曲桿菌抗原(天然提取物)
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。
主要產品包括各種生物單克隆抗原抗體、重組蛋白。
西班牙Certest滅活的空腸彎曲桿菌抗原(天然提取物)
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【產品介紹】
貨號 | 產品名稱 | 規格 | 英文名稱 |
MT-18EH30 | 阿米巴原蟲抗體(克隆H30) | x1mg | Anti-Entamoeba Mab (clone EH30) |
MT-25ETV | 腸道病毒VP1重組蛋白 | x1mg | Enterovirus VP1 recombinant protein |
MT-18EV5 | 腸道病毒抗體(克隆EV5) | x1mg | Anti-Enterovirus Mab (clone EV5) |
MT-25STX | 大腸桿菌O157 VT1重組蛋白 | x1mg | 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-18E10 | 大腸桿菌O157抗體(克隆E10) | x1mg | Anti-E. coli O157 Mab (clone E10) |
MT-18SN3 | 肺炎鏈球菌單克隆抗體(克隆SN3) | x1mg | 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-16CP14 | 鈣結合蛋白單克隆抗體(克隆CP14) | x1mg | Anti-Calprotectin Mab (clone CP14) |
MT-18RV3 | 呼吸道合胞病毒單抗(克隆RV3) | x1mg | 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-25RSV | 呼吸道合胞病毒重組融合蛋白 | x1mg | RSV recombinant fusion protein |
MT-18Y77 | 甲型流感病毒單抗(克隆Y77) | x1mg | Anti-Influenza A Mab (clone Y77) |
MT-25FAN | 甲型流感病毒重組核蛋白 | x1mg | Influenza A recombinant nucleoprotein |
MT-16G18 | 賈第鞭毛蟲抗體(克隆G18) | x1mg | 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-25A1G | 賈第蟲腸道滋養體重組蛋白 | x1mg | Giardia intestinalis trophozoite recombinant protein |
MT-25GCP | 賈第蟲腸囊菌重組蛋白 | x1mg | Giardia intestinalis cyst recombinant protein |
MT-25GDH | 艱難梭菌GDH重組蛋白 | x1mg | Clostridium difficile GDH recombinant protein |
MT-18TA5 | 艱難梭菌毒素A抗(克隆TA5) | x1mg | 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-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-18TB41 | 艱難梭菌毒素B抗(克隆TB41) | x1mg | 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-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-16GD10 | 艱難梭菌抗體(克隆GD10) | x1mg | Anti-GDH Mab (clone GD10) |
MT-25CEP | 空腸彎曲桿菌重組外膜蛋白 | x1mg | Campylobacter jejuni recombinant outer membrane protein |
MT-26VP6 | 輪狀病毒VP6重組蛋白 | x1mg | Rotavirus VP6 recombinant protein |
MT-16R15 | 輪狀病毒單克隆抗體(克隆R15) | x1mg | Anti-Rotavirus Mab (clone R15) |
MT-28SAGU | 滅活A鏈球菌抗原(天然提取物) | x1mg | Inactivated STREP A 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-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-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-28CCU | 滅活的大腸桿菌抗原(天然提取物) | x1mg | Inactivated Campylobacter coli 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-28SPNU | 滅活的肺炎鏈球菌抗原(天然提取物) | x1mg | Inactivated Streptococcus pneumoniae 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-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-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-28LNU | 滅活的嗜肺軍團菌抗原(天然提取物) | x1mg | Inactivated Legionella pneumophila 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-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-28PECU | 滅活的幽門螺桿菌抗原(天然提取物) | x1mg | Inactivated H. pylori 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-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-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-28STU | 滅活傷寒沙門氏菌抗原(天然提取物) | x1mg | Inactivated Salmonella typhi 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-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-29KOE | 滅活小球隱孢子蟲抗原(天然提取物) | x1mg | Inactivated Cryptosporidium parvum antigen (native extract) |
MT-25EDP | 內阿米巴重組蛋白 | x1mg | Entamoeba dispar recombinant protein |
MT-25NGI1 | 諾如病毒GI.1重組P結構域 | x1mg | Norovirus GI.1 recombinant P domain |
MT-31NGA | 諾如病毒GI.1重組VLP | x1mg | Norovirus GI.1 recombinant VLP |
MT-25NGI3 | 諾如病毒GI.3重組P結構域 | x1mg | 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-25NGII17 | 諾如病毒GII.17重組P結構域 | x1mg | 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-31NPA | 諾如病毒GII.4重組VLP | x1mg | Norovirus GII.4 recombinant VLP |
MT-18NP8 | 諾如病毒GII單克隆抗體(克隆NP8) | x1mg | Anti-Norovirus GII Mab (clone NP8) |
MT-18NG28 | 諾如病毒GI單克隆抗體(克隆NG28) | x1mg | Anti-Norovirus GI Mab (clone NG28) |
MT-25HCP | 人類鈣衛蛋白重組蛋白 | x1mg | Human Calprotectin recombinant protein |
MT-29HLF | 人乳鐵蛋白蛋白質(天然提取物) | x1mg | Human Lactoferrin protein (native extract) |
MT-29HHB | 人血紅蛋白蛋白質(天然提取物) | x1mg | Human Haemoglobin 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-20TSS | 溶血性A鏈球菌抗體 | x1mg | Anti-Strep A Pab |
MT-25EHP | 溶組織內阿米巴重組蛋白 | x1mg | Entamoeba histolytica recombinant protein |
MT-16LC16 | 乳鐵蛋白單抗(克隆LC16) | x1mg | Anti-Lactoferrin Mab (clone LC16) |
MT-16LC4 | 乳鐵蛋白單抗(克隆LC4) | x1mg | Anti-Lactoferrin Mab (clone LC4) |
MT-18LN14 | 嗜肺軍團菌單抗(克隆LN14) | x1mg | 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-16CA29 | 彎曲桿菌抗體(克隆ECA29) | x1mg | Anti-Campylobacter Mab (clone CA29) |
MT-25CCP | 彎曲桿菌重組外膜蛋白 | x1mg | Campylobacter coli recombinant outer membrane protein |
MT-25HEX | 腺病毒HEXON重組蛋白 | x1mg | Adenovirus HEXON recombinant protein |
MT-18A14 | 腺病毒單克隆抗體(克隆A14) | x1mg | 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-18A15 | 腺病毒抗體(克隆A15) | x1mg | Anti-Adenovirus Mab (clone A15) |
MT-25HEXR | 腺病毒六鄰體重組蛋白 | x1mg | Adenovirus HEXON recombinant protein |
MT-18AT18 | 星狀病毒單克隆抗體(克隆AT18) | x1mg | 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-25AST | 星狀病毒衣殼重組蛋白 | x1mg | Astrovirus capsid recombinant protein |
MT-16F22 | 血紅蛋白單抗(克隆F22) | x1mg | Anti-Haemoglobin Mab (clone F22) |
MT-18YB91 | 乙型流感病毒單抗(克隆YB91) | x1mg | Anti-Influenza B Mab (clone YB91) |
MT-25FBN | 乙型流感病毒重組核蛋白 | x1mg | Influenza B recombinant nucleoprotein |
MT-18K31 | 隱球菌抗體(克隆K31) | x1mg | Anti-Crypto Mab (clone K31) |
MT-25PCH | 幽門螺桿菌重組外膜蛋白 | x1mg | H. pylori recombinant outer membrane protein |
MT-16P2 | 幽門螺旋桿菌抗體(克隆P2)HP抗體 | x1mg | Anti-H. pylori Mab (clone P2) |
西班牙Certest滅活的空腸彎曲桿菌抗原(天然提取物)
研究團隊首先建立了從尿液細胞、羊水細胞誘導iPS的技術平臺,中國醫學科學院血液學研究所程濤教授研究組建立了外周血細胞無基因插入的episomal方法誘導iPS的技術平臺,北京大學鄧宏魁教授研究組在世界上*在小鼠建立了*利用小分析化合物誘導iPS的技術平臺。這些技術使得建立人誘導全能干細胞更方便、更安全,為今后的臨床應用打下了重要基礎。
同時,課題組建立了多個的疾病ips細胞模型,如帕金森氏疾病、老年癡呆癥、血友病及白血病等疾病iPS細胞模型,并進行了疾病發生發展的研究,為今后的細胞治療、基因治療提供了可靠的科學依據。例如,課題組在小鼠上做了初步嘗試,iPS細胞可以成功分化為視網膜底干細胞,并且移植獲得成功。血友病的基因矯正實驗研究也正在血研所開展。
由于iPS細胞的起始細胞來源于自體細胞,不產生免疫反應,和其他細胞相比,iPS細胞具有更廣闊的潛在臨床應用前景。隨著細胞重編程技術逐漸成熟,iPS細胞已經在逐漸接近臨床應用,我們期待著在未來:通過在體外分化獲得所需要的有功能但沒有致瘤性的目的細胞或干細胞,在移植到患者體內后,治愈一些過去沒有有效治療方法的疾病,特別是遺傳疾病和腫瘤。
新的研究證明,地球上至少有相當一部分水,形成于星際空間,可以追溯到太陽形成之前。這也意味著,太陽系外的其他行星也會在含有大量水的環境中形成,意味著生命在銀河系中遍地開花的前景相當樂觀。圖片來源:阿五,夜空中國
水是地球上生命起源的關鍵物質,對于評估其他行星上是否可能存在生命也相當重要。確定地球上水的zui初來源,是了解養育生命的環境如何形成的關鍵,也是了解其他地方有多大可能性找到類似環境的關鍵。一項新的研究發現,我們太陽系中有許多水,很可能起源于星際空間中形成的冰。他們的研究論文9月25日發表在《科學》(science)雜志上。
在我們的太陽系中,水可以說是無處不在。不只地球上有水,那些冰質彗星和衛星上也有水,甚至連水星上永遠曬不到陽光的陰影盆地中也有水冰的存在。水還存在于來自隕石、月球和火星的礦物樣本之中。尤其是彗星和小行星,由于本身就較為原始,它們為我們太陽系早期的環境提供了天然的“時間膠囊”。
在太陽尚處在幼年時,它被一個原行星盤所包圍,也就是所謂的“太陽星云”(solar nebula),行星便在其中誕生。但是,科學家此前一直不太清楚,太陽星云中的冰,到底來源于太陽形成之前的星際分子云,還是在太陽形成的過程中全部被破壞然后又通過化學反應重新形成的。
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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】 廣州清華科技園創新基地番禺石樓鎮創啟路63號二期2幢101-103室
The research team first established a technology platform for inducing iPS from urine cells and amniotic fluid cells. Professor Cheng Tao of the Institute of Hematology, Chinese Academy of Medical Sciences established a technology platform for induction of iPS by the episomal method of gene insertion without peripheral blood cells. Professor Deng Hongkui of Peking University The research team is the first in the world to set up a technology platform for fully utilizing small analytical compounds to induce iPS in mice. These techniques make it more convenient and safer to establish human-induced totipotent stem cells and lay an important foundation for future clinical applications.
At the same time, the research group established a number of ips cell models of diseases, such as Parkinson's disease, Alzheimer's disease, hemophilia and leukemia and other diseases iPS cell model, and carried out the development of disease research for future cell therapy, Gene therapy provides a reliable scientific basis. For example, the group made a preliminary attempt in mice, iPS cells can be successfully differentiated into stem cells of the retina, and the transplant was successful. Hemophilia gene correction experiments are also carried out by the Institute of Blood.
Since iPS cells originate from autologous cells, the iPS cells do not produce an immune response. Compared with other cells, iPS cells have a broader potential for clinical application. With the gradual maturation of cell reprogramming technology, iPS cells are gradually getting closer to clinical application. We are looking forward to: In the future, by in vitro differentiation to obtain the desired target cells or stem cells with function but not tumorigenicity, After the cure for some past no effective treatment of diseases, especially genetic diseases and tumors.
New research shows that at least some of the Earth's water is formed in interslar space, dating back to the time when the sun was formed. This also means that other planets outside the solar system will also form in an environment that contains a lot of water, which means that the prospect of blooming of life throughout the Milky Way is quite optimistic. Photo Source: Ah Wu, the night sky China
Water is a key material in the origin of life on Earth, and it is important to assess whether life may exist on other planets. Determining the initial source of water on Earth is the key to understanding how the environment for nourishing life forms and how likely it is to find similar environments elsewhere. A new study found that much of the water in our solar system is likely to originate from the formation of ice in interslar space. Their research paper was published in the science magazine on September 25.
Water can be ubiquitous in our solar system. Not only is there water on Earth, there are also water on ice-bound comets and salites, and there is ice in the shaded basins that never reach the sunshine on Mercury. Water is also present in mineral samples from meteorites, the moon and Mars. In particular, comets and asteroids, by their very nature, provide natural "time capsules" for the early environment of our solar system.
When the sun is still in its infancy, it is surrounded by a primitive planet plate, the so-called solar nebula, in which planets are born. However, scientists have been less clear about whether the ice in the solar nebula, in the end, originated from the interslar cloud of clouds before the sun was formed or compley destroyed by the sun's formation and then re-formed by chemical reactions.
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