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西班牙Certest人血紅蛋白蛋白質(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人血紅蛋白蛋白質(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人血紅蛋白蛋白質(天然提取物)
方法技術從來都是科學進步的推動力,三位獲獎者的研究成果發展出了多項納米顯微技術,目前已被世界各地廣泛使用。功能強大的納米顯微鏡所展示的微小世界,也產生了很多前沿認知。斯特凡·黑爾看到了活神經細胞的內部,這能幫助更好地理解大腦突觸;威廉·莫納研究了與亨廷頓氏病相關的蛋白質;而埃里克·貝齊格對胚胎中的細胞分裂進行了跟蹤。類似的例子不勝枚舉。毫無疑問,2014年諾貝爾化學獎得主們所作出的成就,將對*的福祉作出重大貢獻。
研究人員在干細胞成為血液細胞的過程中(該過程稱為造血作用),發現以前未被發現的步驟。一個研究組,包括溫斯洛普教授溫迪·埃伯,已經建立了一個非常復雜的一系列事件確定血液祖細胞群密切相關的命運。
埃伯教授,這項研究的一個共同作者,是西澳大利亞州大學病理學和實驗室醫學學院的負責人。
這項研究,是大型藍圖研究項目中用于了解血液疾病的一部分,識別血液細胞類型之間的基因表達的成千上萬的差異。這些差異導致了許多特定事件,這些事件在血液正常發育中起著至關重要的作用。在這個過程中出錯可能會導致血液疾病,包括白血病。相關文章發表于2014年9月26日的《Science》雜志上。
*生成轉錄因子和其他蛋白質調控這個復雜過程的綜合目錄。這項研究發現,RNA在造血過程中以不同的方式被剪切并粘貼到一起,導致每一個階段的蛋白特定形式。直至本研究,血細胞生成在DNA的水平上有了比較充分的了解。不知道的是,然后DNA上的遺傳信息是如何轉錄生成RNA,導致蛋白的形成。、
“我們已經確定了上千個新的RNA被另一種方式處理的位點,” 劍橋大學實驗血液學和威康信托基金會桑格研究所的教授Willem Ouwehand說。在血細胞發育的RNA的可變剪接的關鍵重要性是,通過研究兩種不同形式的同種轉錄因子在巨核細胞(血小板的的前體細胞)形成中的作用來說明的。
埃伯教授說:“這樣的事件改變了來源于單一基因的蛋白質的數量,結構和行為。替代蛋白可促進干細胞轉化為不同的成熟血細胞。”
這項研究所需的造血干細胞和其他細胞沒有被先前的人們研究的很詳細,是因為它們在成人的骨髓中極為罕見。埃伯教授說:“在這項研究中,我們能夠從捐贈的臍帶血中純化出這些細胞,這些祖細胞在臍帶血中的濃度高得驚人。”
西班牙Certest人血紅蛋白蛋白質(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
Methodology has always been the driving force of scientific progress, the three winners of the research results developed a number of nano-microscopy, has been widely used around the world. The tiny world displayed by powerful nano-microscopes also generates a lot of cutting-edge awareness. Stefan Hale sees the inside of living nerve cells, which helps to better understand brain synapses; William Mona studied proteins associated with Huntington's disease; and Eric Bezig on embryos The cell division was followed. There are many similar examples. Undoubtedly, the achievements made by 2014 Nobel Laureates in Chemistry will make a significant contribution to the well-being of all humanity.
Researchers in the stem cells into blood cells (the process known as hematopoietic), found that previously undiscovered steps. An international study group, including Wendy Eppe, of Winthrop, has established a very complex series of events that determine the fate of closely related blood progenitor populations.
Professor Eber, co-author of the study, is the head of Western Australia's College of Pathology and Laboratory Medicine.
This study, which is part of a large international blueprint research project used to understand blood diseases, identifies thousands of differences in gene expression between blood cell types. These differences lead to a number of specific events that play a crucial role in the normal development of blood. Errors in the process can lead to blood diseases, including leukemia. A related article was published in the September 26, 2014 issue of Science.
For the first time a comprehensive list of transcription factors and other protein-regulated complex processes is generated. The study found that RNA is sheared and pasted together in different ways during hematopoiesis, resulting in a protein-specific form of each stage. Up to this study, hematopoiesis was well understood at the DNA level. I do not know is how the genetic information on the DNA is then transcribed into RNA, leading to the formation of the protein. ,
"We have identified thousands of new RNAs that are treated differently by another approach," said Willem Ouwehand, a professor of experimental hematology at the University of Cambridge and the Sanger Institute of Wellcome Trust. The crucial importance of alternative splicing of RNA in blood cell development is illustrated by studying the role of two different forms of the same transcription factor in the formation of megakaryocytes (plaet precursors).
Professor Eber said: "Such events change the number, structure and behavior of proteins that originate from a single gene, and alternative proteins can promote the conversion of stem cells into different mature blood cells."
The hematopoietic stem cells and other cells needed for this study have not been studied in great detail by previous studies because they are extremely rare in adult bone marrow. Professor Eber said: "In this study, we were able to purify these cells from donated umbilical cord blood. The progenitor cells were unusually high in umbilical cord blood."
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