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西班牙Certest滅活的大腸桿菌抗原(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滅活的大腸桿菌抗原(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
ohn Cooke教授表示,據我們所知,本文研究是*利用小分子和蛋白來完成治療細胞類型的分化轉移,在特殊情況下我們就可以將成纖維細胞轉化成為所需的細胞類型。文章中研究者首先將成纖維細胞暴露于多聚胞苷酸(polyinosinic-polycytidylic acid,poly I:C)中,雙鏈RNA分子的一小部分會結合宿主細胞的TLR3(toll樣受體3)來“哄騙”細胞好像針對病毒攻擊那樣產生反應;在2012年發表在Cell上的一篇研究文章中,Cooke教授就揭示了成纖維細胞對病毒攻擊的反應,在利用poly I:C處理成纖維細胞后,研究者觀察到了細胞核染色質的重新組裝,這種組裝可以使得之前關閉的基因重新表達,隨后利用諸如VEGF等因子對成纖維細胞進行處理,就可以將少量分化的細胞轉化成為內皮細胞。
在這項研究中,研究者報道可以將2%的成纖維細胞轉化成為內皮細胞,這種比例可以和其它利用病毒及基因療法得到的轉化率等同,但Cooke補充道,目前我們可以使得轉化率高達15%;我們并不想讓所有的成纖維細胞都發生轉化,因為成纖維細胞還發揮著非常重要的作用,文章中我們只是促進部分的抗原抗體細胞轉化成為血管細胞,從而為損傷組織提供血液供給。
隨著研究的深入,研究者將已經轉化的人類細胞(血管細胞)引入到免疫缺陷的小鼠機體中,這些小鼠下肢的血液流動較差,研究者發現人類的血管細胞可以增加小鼠下肢的血管數量,有效改善其血液循環。這些血管細胞可以自發形成血管組織;下一步研究人員想去研究是否其可以拯救受傷的動物,如果該療法可以通過增加受損組織的血液流動從而達到治愈的目的,那么其或許就為開發治療局部缺血等一系列疾病的新型療法提供希望。
食道癌是癌癥死亡的第六大原因,是存活zui少的癌癥之一,食道癌在不同人口中的發病率顯示出巨大的差異,這就表明環境或生活方式是可以控制減少這些疾病風險的因素。
食道上皮惡性腫瘤有兩個主要的病理類型,即鱗狀細胞癌和腺癌。zui近,在發達國家腺癌發病率正在增加,在美國50%以上是腺癌,尤其是在白人男性,約為70%是腺癌。食管腺癌發生在食管的下部。與此形成鮮明對比的是,在日本,腺癌的增加并不清楚,大多數(90%)的食管癌都是鱗狀細胞癌,這樣的鱗狀細胞癌大多發生在食管中段,60%或更多的食道癌也發生在中部和上部。這些差異都會影響治療的結果。
日本岐阜市醫院診斷病理學Naoki Watanabe通過對食道癌組織病理學特點及分子機制的概述,討論了食道的致癌作用,文章發表在科研出版社英文期刊《Open Journal of Pathology》(病理學期刊)2014年10月刊上。
西班牙Certest滅活的大腸桿菌O157抗原(天然提取物)
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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
Professor Ohn Cooke said that, to our knowledge, this study is the first to utilize small molecules and proteins to complete the differentiation and metastasis of treated cell types. Under special circumstances, we can transform fibroblasts into desired cell types. In the article, researchers first exposed fibroblasts to polyinosinic-polycytidylic acid (poly I: C), and a small portion of the double-stranded RNA molecule binds to the host cell's TLR3 (toll-like receptor 3) "Kidding" cells seem to react as they did to virus attacks; in a research article published in the Cell in 2012, Professor Cooke revealed the fibroblast response to viral challenge by treating fibroblasts with poly I: C After the researchers observed a reassembly of the chromatin in the nucleus, this assembly allows the previously closed gene to be re-expressed, followed by treatment of fibroblasts with factors such as VEGF, which can transform small numbers of differentiated cells into endothelial cells.
In this study, researchers report that 2% of fibroblasts can be transformed into endothelial cells, which is equivalent to other rates of virus and gene therapy conversion, but Cooke added that we can now convert Up to 15%. We do not want to transform all the fibroblasts because fibroblasts play a very important role. In this article, we only promote part of the antigen-antibody cells into blood vessels to provide blood to damaged tissues supply.
With further research, researchers introduced already transformed human cells (vascular cells) into immunocompromised mice. The blood flow in the lower extremities of these mice was poor. The researchers found that human vascular cells can increase the number of lower extremities The number of blood vessels, effectively improve their blood circulation. These vascular cells spontaneously develop into vascular tissue; the next step researchers want to investigate is whether it can save an injured animal, and if the therapy can be cured by increasing the blood flow in the damaged tissue for the purpose of healing Ischemia and a series of new diseases such as therapies provide hope.
Esophageal cancer is the sixth leading cause of cancer deaths and one of the least survivors of cancer. The incidence of esophageal cancer in different populations shows a huge difference, indicating that the environment or lifestyle is the factor that can control the risk of reducing these diseases .
Esophageal malignancies have two major pathological types, squamous cell carcinoma and adenocarcinoma. Recently, the incidence of adenocarcinoma is increasing in developed countries, with more than 50% of adenocarcinomas in the United States, especially in white men, and about 70% are adenocarcinomas. Esophageal adenocarcinoma occurs in the lower part of the esophagus. In sharp contrast, in Japan, the increase in adenocarcinoma is not clear, and most (90%) of esophageal cancers are squamous cell carcinomas. Most of these squamous cell carcinomas occur in the middle of the esophagus, and 60% or More esophageal cancer also occurs in the middle and upper part. These differences will affect the outcome of treatment.
Diagnostic Pathology in Gifu City, Japan Naoki Watanabe discusses the carcinogenicity of the esophagus through an overview of the histopathological features and molecular mechanisms of esophageal cancer. The article was published in the journal Open Journal of Pathology 2014 In October issue.
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