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Certest星狀病毒單克隆抗體(克隆AT18)

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產品型號Anti-Astrovirus Mab

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更新時間:2022-11-29 10:15:33瀏覽次數:678次

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Certest公司 Anti-Astrovirus Mab Certest星狀病毒單克隆抗體(克隆AT18) 需要了解西班牙Certest的產品可以,本產品由廣州健侖生物供應。

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

Certest公司 

想了解更多的產品及服務請掃描下方二維碼:

【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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