2ml單價(jià)O變形桿菌診斷血清 OXK

廣州健侖生物科技有限公司

我司長(zhǎng)期供應(yīng)尼古?。商鎸帲z測(cè)試劑盒，違禁品檢測(cè)試劑盒，單卡檢測(cè)，3聯(lián)卡到12聯(lián)卡，可以自由組合，根據(jù)您的需求自由組合，*，性價(jià)比高，產(chǎn)品質(zhì)量很好。

保存要求：除了有特殊說(shuō)明，免疫檢測(cè)產(chǎn)品應(yīng)保存在2-8°C

產(chǎn)品規(guī)格：2ml/瓶

保質(zhì)期：2年

本試劑盒主要用于對(duì)病菌細(xì)菌進(jìn)行檢測(cè)，利用快速玻片凝集檢測(cè)技術(shù)

利用快速玻片凝集和對(duì)流免疫電泳(CIE)鑒定流感嗜血桿菌

2ml單價(jià)O變形桿菌診斷血清 OXK

我司還有很多種血清學(xué)診斷血清、血液檢測(cè)、免疫檢測(cè)產(chǎn)品、毒素檢測(cè)、凝集檢測(cè)、酶免檢測(cè)、層析檢測(cè)、免疫熒光檢測(cè)產(chǎn)品，。

（ MOB：楊永漢）

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【公司名稱】 廣州健侖生物科技有限公司
【市場(chǎng)部】    楊永漢

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【騰訊  】 
【公司地址】 廣州清華科技園創(chuàng)新基地番禺石樓鎮(zhèn)創(chuàng)啟路63號(hào)二期2幢101-103

大腸桿菌核糖體蛋白的初級(jí)結(jié)構(gòu)均被確定。核糖體蛋白核糖體蛋白大腸桿菌核糖體的S亞基含S—S共種蛋白質(zhì)，S亞基含L—L共種蛋白質(zhì)。這些蛋白質(zhì)已被全部分離純化。分子量約萬(wàn)到萬(wàn)。除S、L、L之外全是堿性蛋白質(zhì)。這些蛋白質(zhì)是免疫學(xué)上獨(dú)立的蛋白質(zhì)，只有L、L顯示出相互交叉反應(yīng)。
The primary structure of E. coli ribosomal protein was determined. The ribosomal protein ribosomal protein S-subunit of the E. coli ribosome contains the S-S co-species protein and the S subunit contains the L-L co-species protein. All of these proteins have been isolated and purified. About 10,000 to 10,000 molecular weight. Except for S, L, and L, all are basic proteins. These proteins are immunologically independent proteins and only L and L show cross-reactions.

 用已知種類的熒光抗體浸染待檢的含有抗原的細(xì)胞或組織切片，如有相應(yīng)抗原存在，則抗原即與此種抗體發(fā)生特異性結(jié)合，形成復(fù)合物而粘著在細(xì)胞上，不易洗脫，在熒光顯微鏡下成為發(fā)出熒光的可見物，可達(dá)到診斷或定位的目的。包括直接法和間接法。．酶聯(lián)免疫吸附試驗(yàn)。本法的原理是利用酶（常用辣根過(guò)氧化物酶）標(biāo)記的抗原或抗體，以測(cè)定被檢標(biāo)本中有無(wú)相應(yīng)的抗原或抗體。有間接法、雙抗體法、競(jìng)爭(zhēng)法三種。．溶血空斑試驗(yàn)。．免疫印跡技術(shù)。免疫印跡或免疫轉(zhuǎn)印技術(shù)(immunoblotting或Westernblot）是在Southern()抗體抗原反應(yīng)創(chuàng)建的DNA印跡術(shù)(Southernblotting）基礎(chǔ)上發(fā)展起來(lái)的新型免疫生化技術(shù)。細(xì)胞免疫檢測(cè)法近代免疫學(xué)廣泛采用了細(xì)胞生物學(xué)、免疫血清學(xué)、免疫標(biāo)記、免疫組化等多方面技術(shù)，不斷發(fā)展和完善了一系列細(xì)胞免疫檢測(cè)技術(shù)，用于檢測(cè)各類免疫細(xì)胞的表面標(biāo)志（包括抗原及受體）、細(xì)胞的活化、增殖、吞噬、殺傷功能、各種細(xì)胞因子的活性或含量等方面。這些技術(shù)為深入研究和認(rèn)識(shí)機(jī)體免疫系統(tǒng)的生理、病理改變，闡明某些疾病的發(fā)病機(jī)制和臨床診治提供了有用的手段。隨著細(xì)胞免疫學(xué)的迅猛發(fā)展，時(shí)有新的細(xì)胞免疫檢測(cè)技術(shù)出現(xiàn)。
The antigen-containing cells or tissue sections to be detected are impregnated with a known type of fluorescent antibody. If there is a corresponding antigen, the antigen specifically binds to the antibody and forms a complex that adheres to the cells and does not elute easily. Under the fluorescence microscope, it becomes a visible object that emits fluorescence and can be used for diagnosis or positioning. Including direct and indirect methods. . Enzyme-linked immunosorbent assay. The principle of this method is to use an enzyme (common horseradish peroxidase) labeled antigen or antibody to determine whether there is a corresponding antigen or antibody in the test sample. There are three kinds of indirect method, double antibody method and competition method. . Hemolysis plaque assay. . Immunoblotting technique. Western blotting or immunoblotting (immunoblotting or Western blot) is a new type of immune biochemistry developed on the basis of Southern blotting created by Southern () antibody antigen reaction. Cellular Immunoassay Methods Modern immunology has extensively used cell biology, immunological serology, immunolabeling, and immunohistochemistry to develop and perfect a series of cellular immunoassay techniques for the detection of various immune cell surfaces. Signs (including antigens and receptors), cell activation, proliferation, phagocytosis, killing function, activity or content of various cytokines. These technologies provide useful tools for the in-depth study and understanding of the physiological and pathological changes of the body's immune system, and clarify the pathogenesis and clinical diagnosis and treatment of certain diseases. With the rapid development of cellular immunology, new cellular immunoassay techniques have emerged.