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西班牙Certest星狀病毒單克隆抗體(克隆AT18)
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。
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。
Certest公司 Certest星狀病毒單克隆抗體(克隆AT18)
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【西班牙Certest生物原料】
貨號 | 產品名稱 | 規格 | 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-18A15 | 腺病毒抗體(克隆A15) | x1mg | 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-18AT8 | 星狀病毒單克隆抗體(克隆AT8) | x1mg | 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-18NP8 | 諾如病毒GII單克隆抗體(克隆NP8) | x1mg | Anti-Norovirus GII Mab (clone NP8) |
MT-18EV5 | 腸道病毒抗體(克隆EV5) | x1mg | 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-16GD10 | 艱難梭菌抗體(克隆GD10) | x1mg | 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-18TA7 | 艱難梭菌毒素A抗(克隆TA7) | x1mg | 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-18TB48 | 艱難梭菌毒素B抗(克隆TB48) | x1mg | 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-16CA29 | 彎曲桿菌抗體(克隆ECA29) | x1mg | Anti-Campylobacter Mab (clone CA29) |
MT-18K31 | 隱球菌抗體(克隆K31) | x1mg | 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-16G22 | 賈第鞭毛蟲抗體(克隆G22) | x1mg | 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-16CP14 | 鈣結合蛋白單克隆抗體(克隆CP14) | x1mg | Anti-Calprotectin Mab (clone CP14) |
MT-16F22 | 血紅蛋白單抗(克隆F22) | x1mg | Anti-Haemoglobin Mab (clone F22) |
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-26VP6 | 輪狀病毒VP6重組蛋白 | x1mg | Rotavirus VP6 recombinant protein |
MT-25HEX | 腺病毒HEXON重組蛋白 | x1mg | Adenovirus HEXON recombinant protein |
MT-25AST | 星狀病毒衣殼重組蛋白 | x1mg | 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-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-25ETV | 腸道病毒VP1重組蛋白 | x1mg | 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-25GDH | 艱難梭菌GDH重組蛋白 | x1mg | 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-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-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-25CCP | 彎曲桿菌重組外膜蛋白 | x1mg | 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-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-25EDP | 內阿米巴重組蛋白 | x1mg | Entamoeba dispar recombinant protein |
MT-25EHP | 溶組織內阿米巴重組蛋白 | x1mg | Entamoeba histolytica recombinant protein |
MT-25HCP | 人類鈣衛蛋白重組蛋白 | x1mg | Human Calprotectin recombinant protein |
MT-31NGA | 諾如病毒GI.1重組VLP | x1mg | Norovirus GI.1 recombinant VLP |
MT-31NPA | 諾如病毒GII.4重組VLP | x1mg | 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-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-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-28SEU | 滅活腸炎沙門氏菌抗原(天然提取物) | x1mg | 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-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-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-28STU | 滅活傷寒沙門氏菌抗原(天然提取物) | x1mg | 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-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-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-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-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-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-29KOE | 滅活小球隱孢子蟲抗原(天然提取物) | x1mg | 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-29HLF | 人乳鐵蛋白蛋白質(天然提取物) | x1mg | 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-20TSS | 溶血性A鏈球菌抗體 | x1mg | 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-18RV4 | 呼吸道合胞病毒單抗(克隆RV4) | x1mg | 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-18A15 | 腺病毒單克隆抗體(克隆A15) | x1mg | 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-18YB91 | 乙型流感病毒單抗(克隆YB91) | x1mg | 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-18LN29 | 嗜肺軍團菌單抗(克隆LN29) | x1mg | 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-18SN4 | 肺炎鏈球菌單克隆抗體(克隆SN4) | x1mg | 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-25HEXR | 腺病毒六鄰體重組蛋白 | x1mg | Adenovirus HEXON recombinant protein |
MT-25FAN | 甲型流感病毒重組核蛋白 | x1mg | Influenza A recombinant nucleoprotein |
MT-25FBN | 乙型流感病毒重組核蛋白 | x1mg | 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-29RVV | 滅活呼吸道合胞病毒抗原(天然提取物) | x1mg | 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-28SPNU | 滅活的肺炎鏈球菌抗原(天然提取物) | x1mg | Inactivated Streptococcus pneumoniae antigen (native extract) |
Certest公司
細胞質
對細胞質的認識落后于對細胞核或染色體的認識,而且經歷很長時期才得到改善。
1、1865年,C.弗羅曼認為細胞中含有纖維狀物質交織成框架或網狀。
2、1875年,德國生物學家O.赫特維希發現了中心體。
3、1882年,W.弗勒明錯誤地把所看到的線粒體、紡錘絲以及固定樣品中的其他纖維狀構造推而廣之,認為細胞質是由埋藏在基質中的這些絲狀成分構成的。
4、1886年,德國組織學家R.阿爾特曼甚至認為一定的小顆粒是zui簡單的、活的、“細胞的基本有機體”,由于它們的特殊方式的集聚而構成細胞;這可能也是由于誤認了線粒體以及分泌和貯藏顆粒。
5、1888年,德國動物學家O.比奇利提出了蜂窩或泡沫學說,即:細胞質是由較粘的物質(透明質hyalopla-sm)形成的精細的蜂窩狀構造構成的,其中充滿另一種稱之為細胞液(enchylema)的物質。這個學說在一定程度上符合實際情況,也比較容易被人接受,因為比奇利不是根據對固定的標本觀查,而是根據對原生動物的活體觀察提出的。(注:原生動物太陽蟲的細胞質確實是泡沫狀的──關于原生動物是否單細胞的問題爭論了差不多半個世紀,直到1875年經比奇利研究纖毛蟲后才予以肯定──因此泡沫狀學說維持的時間zui長。)
6、1895年,高爾基發現了被他稱之為Apparato reticulare interno的網狀結構物質(后稱:高爾基器)。
7、1897年,C.本達發現了線粒體并命名,對于它的存在意見比較*。在一些細胞中經一定的固定劑固定后,可被一定的染料染色,也可在活體中觀察到。但是在光學顯微鏡下其形狀各式各樣,或是線狀或是顆粒狀或是一串顆粒;至于是否存在于動物的各種細胞內或一切生物體的細胞內,當時還沒有定論。
8、1899年,加尼耶在研究各類腺體細胞時發現細胞質中含有嗜堿性的呈現動態變化的絲狀或棒狀的結構,認為這不是細胞質的內含物,而是細胞質的組成部分,因而命名為動質(后稱內質網),并且對此做了詳細的敘述。
進入20世紀之后,尤其是電子顯微鏡得到廣泛使用,標本的包埋、切片一套技術逐漸完善,才有了很大改變。通過大量的工作,不僅弄清楚了從前在光學顯微鏡下可以看到而又看不清,或者尚有爭議的細胞器,如線粒體、高爾基器、中心體、內質網、纖毛、鞭毛等構造,而且還發現了許多從前未曾看到過的構造如溶酶體、過氧化酶體、核糖體以及構成細胞骨架的各種纖維物質。
細胞膜
20世紀40年代后,利用高壓電鏡觀察到了由 1~10埃粗細的纖維組成的支撐著各種細胞器的微梁系統,而且看到了細胞的各種膜。在電鏡下斷定了所有的膜都是 75~100埃厚的三層結構(稱之為單位膜)。不僅如此,一個細胞的各部分膜都是相連的,質膜與內質網,內質網與高爾基器或核膜相連。核膜是雙層的,由內外兩層膜構成,并且具有有一定結構的核膜孔,通過它,細胞質的物質和細胞核的物質得以交流。在質膜上還發現了細胞間連結:橋粒、緊密連接和間隙連接等。這些結構與細胞間的結合或細胞間的物質交流有關;利用冰凍蝕刻技術,可以更好地觀察它們。
推動核酸檢測試劑盒
細胞學的研究,在相當程度上受到其他學科的推動,根據各學科的影響大致地可以劃分幾個階段,當然這些階段不可能截然分開。
胚胎學
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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
Cytoplasm
Understanding of the cytoplasm behind the understanding of the nucleus or chromosome, and only after a long period of time to be improved.
1, 1865, C. Foerman believes that the cells contain fibrous material interwoven into a framework or reticular.
In 1875, the German biologist O. Hertwich found the centrosome.
3. In 1882, W. Fleming mistakenly viewed the mitochondria, spindle filaments and other fibrous structures seen in fixed samples by mistake, believing that the cytoplasm consisted of these filamentous components buried in the matrix .
4. In 1886, the German histologist R. Altman even considered certain small particles to be the simplest, living, "basic organism of cells" that, because of their particular manner of aggregation, formed cells; this could also be due to Mistaken for mitochondria and secreted and stored particles.
5. In 1888, the German zoologist O. Beechley proposed the cellular or foam theory that the cytoplasm consists of a fine, honeycomb-like structure made of a more viscous material (hyaloplast-sm) A substance called enchylema. This doctrine to a certain extent in line with the actual situation, but also relatively easy to be accepted, because Beechley is not based on a fixed specimen examination, but on the protozoan live observations made. (Note: The cytoplasm of protozoan sun bugs is indeed foamy - arguing for about a half century whether the protozoan is single-celled or not until affirmative in 1875 after studying ciliates in Beechley - Doctrine persists for the longest time.)
6, 1895, Gorky found what he called Apparato reticulare interno mesh material (later: Golgi apparatus).
7, 1897, C. Benda found mitochondria and named, for its existence is more consistent opinion. In some cells by a fixed fixative, can be a certain dye staining, but also observed in living. But under the light microscope its shape is varied, either linear or granular or a string of particles; as to whether it exists in various animal cells or cells of all living organisms, was not conclusive at the time.
8, 1899, Garnier in the study of various types of glandular cells found in the cytoplasm containing basophilic dynamic changes in the filamentous or rod-shaped structure, that this is not a cytoplasmic inclusion, but a component of the cytoplasm , Hence its name verb (later referred to as the endoplasmic reticulum), and described in detail.
Into the 20th century, especially the widespread use of electron microscopy, specimen embedding, slicing a set of technologies gradually improved, only a great change. Through a great deal of work, not only can we see clearly the structure of the organelles, such as mitochondria, Golgi apparatus, centrosome, endoplasmic reticulum, cilia, A number of other previously unknown structures such as lysosomes, peroxisomes, ribosomes, and various fibrous materials that make up the cytoskeleton have also been discovered.
Cell membrane
After the 1940s, a microbeam system supporting various organelles consisting of 1 to 10 angstrom thick fibers was observed by high-pressure electron microscopy and various membranes of cells were seen. Electron microscopy concluded that all membranes were three-layer structures of 75-100 angstroms thick (called unit membranes). Not only that, all parts of a cell membrane are connected, the plasma membrane and the endoplasmic reticulum, endoplasmic reticulum and Golgi apparatus or the nuclear membrane connected. The nuclear membrane is double-layered, composed of two layers of membranes, inside and outside, and has a structured nuclear membrane pore through which cytoplasmic and nuclear substances are exchanged. Interstitial cells were also found on the plasma membrane: desmosomes, tight junctions and gap junctions. These structures are associated with cell-cell binding or cell-to-cell material exchange; they can be better visualized using freeze-etching techniques.
Promote nucleic acid testing kits
Cytological research, to a considerable extent by other disciplines to promote, according to the impact of various disciplines can be divided into several stages, of course, these stages can not be compley separated.
Embryology
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