變形桿菌血清型鑒定OX2

廣州健侖生物科技有限公司

我司長期供應(yīng)尼古?。商鎸帲z測試劑盒，違禁品檢測試劑盒，單卡檢測，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，*，性價比高，產(chǎn)品質(zhì)量很好。

保存要求：除了有特殊說明，免疫檢測產(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病菌細菌進行檢測，利用快速玻片凝集檢測技術(shù)

利用快速玻片凝集和對流免疫電泳(CIE)鑒定流感嗜血桿菌

2ml單價變形桿菌診斷血清 OX19

2ml單價變形桿菌診斷血清 OX19

2ml單價O桿菌診斷血清 OXK

2ml單價O桿菌診斷血清 OXK

變形桿菌凝集抗血清診斷-試劑盒

變形桿菌凝集抗血清診斷-試劑盒

變形桿菌血清型鑒定OX2

變形桿菌屬（Proteus）也是腸桿菌科成員，現(xiàn)有5個種，普通變形桿菌、奇異變形桿菌、產(chǎn)黏變形桿菌、潘氏變形桿菌和豪氏變形桿菌。其中普通變形桿菌（P. vulgaris）和奇異變形桿菌（P. mirabilis）與臨床關(guān)系較為密切。
變形桿菌食物中毒是我國常見的食物中毒之一，引起食物中毒的變形桿菌主要是普通變形桿菌(P．vulgaris)和奇異變形桿菌(P．mirabikis)。過去，變形桿菌食物中毒還包括普羅威登斯菌屬(Providencid)中的雷氏普羅威登斯菌(P．rettgeri)及摩根菌屬(Morganella)中的摩氏摩根菌(M．morganii)食物中毒。普通變形桿菌、奇異變形桿菌分別有100多個血清型，雷氏普羅威登斯菌有93個血清型，摩氏摩根菌有75個血清型。變形桿菌屬于菌，一般不致病，需氧或兼性厭氧，其生長繁殖對營養(yǎng)要求不高，在4～7℃即可繁殖，屬低溫菌。因此，此菌可以在低溫儲存的食品中繁殖。變形桿菌對熱抵抗力不強，加熱55℃持續(xù)1h可被殺滅。

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

（ MOB：楊永漢）

我司還提供其它進口或國產(chǎn)試劑盒：登革熱、瘧疾、流感、A鏈球菌、合胞病毒、腮病毒、乙腦、寨卡、黃熱病、基孔肯雅熱、克錐蟲病、違禁品濫用、肺炎球菌、軍團菌、化妝品檢測、食品安全檢測等試劑盒以及日本生研細菌分型診斷血清、德國SiFin診斷血清、丹麥SSI診斷血清等產(chǎn)品。

想了解更多的產(chǎn)品及服務(wù)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

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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號二期2幢101-103

E-花環(huán)法。人類T細胞表面有羊細胞受體(CD）能與羊紅細胞結(jié)合形成玫瑰花樣結(jié)構(gòu)。即將分離液分離出的外周的單個核細胞懸液與羊紅細胞在體外混合，經(jīng)℃培養(yǎng)～分鐘后放℃過夜，取細胞懸液計數(shù)，外周血淋巴細胞中約%～%淋巴細胞結(jié)成花環(huán)即為T細胞，此法可用來分離T細胞。．T細胞亞群檢測。．細胞毒試驗。Tc細胞、NK細胞、LAK細胞、TIL細胞等對其靶細胞有直接的細胞毒（殺傷）作用。抗體制備常用的檢測方法是Cr（鉻）釋放法，將Cr-NaCrO鹽水溶液與靶細胞（不同的細胞需不同的靶細胞，如NK細胞的靶細胞為K），于℃培養(yǎng)小時左右，Cr即進入靶細胞，與胞漿結(jié)合，洗去游離的Cr后，即可得到Cr標記的靶細胞，將待測細胞毒的細胞與Cr標記的靶細胞混合（比例約為:或:），靶細胞殺傷越多，釋放到上清液中的游離Cr就越多，且不能再被其他細胞吸收，用γ射線測量儀檢測上清液中的cm值，可計算出待檢細胞殺傷活性高低。細胞毒的檢測對腫瘤免疫有較大價值。．巨噬細胞吞噬功能的測定。將中藥(%斑蝥）乙醇浸出液浸漬的濾紙（cm大?。┲糜谑茉囌咔氨矍鼈?cè)皮膚上，～小時后取下濾紙。小時內(nèi)皮膚局部可水泡，內(nèi)含巨噬細胞。取水泡液.ml加雞紅細胞懸液.ml，℃經(jīng)分鐘后作涂片、染色與鏡檢，計算吞噬百分率及每個巨噬細胞吞噬雞紅細胞的平均數(shù)。
E-garland method. There is a sheep cell receptor (CD) on the surface of human T cells that can be combined with sheep erythrocytes to form a rose-like structure. The peripheral mononuclear cell suspension separated from the separation liquid was mixed with sheep erythrocytes in vitro. The cells were incubated for one minute at °C and then allowed to stand at °C overnight. The cell suspension was counted and about % to % lymphocytes in the peripheral blood lymphocytes were garlanded. That is T cells, this method can be used to isolate T cells. . T-cell subset detection. . Cytotoxicity test. Tc cells, NK cells, LAK cells, TIL cells, etc. have a direct cytotoxic (killing) effect on their target cells. The commonly used detection method for antibody preparation is Cr (chromium) release method. Cr-NaCrO saline solution and target cells (different cells require different target cells, such as NK cell target cells for K), incubate at about °C, Cr Into the target cells, combined with the cytoplasm, washed free Cr, you can get the Cr labeled target cells, the test cytotoxic cells and Cr labeled target cells mixed (ratio of about: or:), the target The more cell killing, the more free Cr released into the supernatant and can no longer be absorbed by other cells. The cm value in the supernatant can be measured with a gamma ray measuring instrument to calculate the killing activity of the cells to be examined. The detection of cytotoxicity is of great value for tumor immunity. . Determination of phagocytic function of macrophages. The filter paper (cm size) impregnated with the ethanol extract of the Chinese herbal medicine (%Spotted turtle) was placed on the skin of the forearm flexor skin of the subject, and the filter paper was removed after -hours. Within a few hours, the skin can be blisters and contains macrophages. Take blisters.ml plus chicken erythrocyte suspension.ml, °C, smear, staining and microscopy after minutes, calculate the percentage of phagocytosis and the average number of chicken erythrocytes engulfed by each macrophage.