变形杆菌血清型鉴定OX2

变形杆菌血清型鉴定OX2

广州健仑生物科技有限公司

我司长期供应尼古丁（可替宁）检测试剂盒，违禁品检测试剂盒，单卡检测，3联卡到12联卡，可以自由组合，根据您的需求自由组合，*，性价比高，产品质量很好。

保存要求：除了有特殊说明，免疫检测产品应保存在2-8°C

产品规格：2ml/瓶

保质期：2年

本试剂盒主要用于对病菌细菌进行检测，利用快速玻片凝集检测技术

利用快速玻片凝集和对流免疫电泳(CIE)鉴定流感嗜血杆菌

2ml单价变形杆菌诊断血清 OX19

2ml单价变形杆菌诊断血清 OX19

2ml单价O杆菌诊断血清 OXK

2ml单价O杆菌诊断血清 OXK

变形杆菌凝集抗血清诊断-试剂盒

变形杆菌凝集抗血清诊断-试剂盒

变形杆菌血清型鉴定OX2

变形杆菌属（Proteus）也是肠杆菌科成员，现有5个种，普通变形杆菌、奇异变形杆菌、产黏变形杆菌、潘氏变形杆菌和豪氏变形杆菌。其中普通变形杆菌（P. vulgaris）和奇异变形杆菌（P. mirabilis）与临床关系较为密切。
变形杆菌食物中毒是我国常见的食物中毒之一，引起食物中毒的变形杆菌主要是普通变形杆菌(P．vulgaris)和奇异变形杆菌(P．mirabikis)。过去，变形杆菌食物中毒还包括普罗威登斯菌属(Providencid)中的雷氏普罗威登斯菌(P．rettgeri)及摩根菌属(Morganella)中的摩氏摩根菌(M．morganii)食物中毒。普通变形杆菌、奇异变形杆菌分别有100多个血清型，雷氏普罗威登斯菌有93个血清型，摩氏摩根菌有75个血清型。变形杆菌属于菌，一般不致病，需氧或兼性厌氧，其生长繁殖对营养要求不高，在4～7℃即可繁殖，属低温菌。因此，此菌可以在低温储存的食品中繁殖。变形杆菌对热抵抗力不强，加热55℃持续1h可被杀灭。

我司还有很多种血清学诊断血清、血液检测、免疫检测产品、毒素检测、凝集检测、酶免检测、层析检测、免疫荧光检测产品，。

（ MOB：杨永汉）

我司还提供其它进口或国产试剂盒：登革热、疟疾、流感、A链球菌、合胞病毒、腮病毒、乙脑、寨卡、黄热病、基孔肯雅热、克锥虫病、违禁品滥用、肺炎球菌、军团菌、化妆品检测、食品安全检测等试剂盒以及日本生研细菌分型诊断血清、德国SiFin诊断血清、丹麦SSI诊断血清等产品。

想了解更多的产品及服务请扫描下方二维码：

【公司名称】 广州健仑生物科技有限公司
【市场部】    杨永汉

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【腾讯  】 
【公司地址】 广州清华科技园创新基地番禺石楼镇创启路63号二期2幢101-103

E-花环法。人类T细胞表面有羊细胞受体(CD）能与羊红细胞结合形成玫瑰花样结构。即将分离液分离出的外周的单个核细胞悬液与羊红细胞在体外混合，经℃培养～分钟后放℃过夜，取细胞悬液计数，外周血淋巴细胞中约%～%淋巴细胞结成花环即为T细胞，此法可用来分离T细胞。．T细胞亚群检测。．细胞毒试验。Tc细胞、NK细胞、LAK细胞、TIL细胞等对其靶细胞有直接的细胞毒（杀伤）作用。抗体制备常用的检测方法是Cr（铬）释放法，将Cr-NaCrO盐水溶液与靶细胞（不同的细胞需不同的靶细胞，如NK细胞的靶细胞为K），于℃培养小时左右，Cr即进入靶细胞，与胞浆结合，洗去游离的Cr后，即可得到Cr标记的靶细胞，将待测细胞毒的细胞与Cr标记的靶细胞混合（比例约为:或:），靶细胞杀伤越多，释放到上清液中的游离Cr就越多，且不能再被其他细胞吸收，用γ射线测量仪检测上清液中的cm值，可计算出待检细胞杀伤活性高低。细胞毒的检测对肿瘤免疫有较大价值。．巨噬细胞吞噬功能的测定。将中药(%斑蝥）乙醇浸出液浸渍的滤纸（cm大小）置于受试者前臂屈侧皮肤上，～小时后取下滤纸。小时内皮肤局部可水泡，内含巨噬细胞。取水泡液.ml加鸡红细胞悬液.ml，℃经分钟后作涂片、染色与镜检，计算吞噬百分率及每个巨噬细胞吞噬鸡红细胞的平均数。
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.