詳細(xì)介紹
流感嗜血桿菌診斷血清(6種血清型價(jià)格)
廣州健侖生物科技有限公司
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),,對(duì)大腸桿菌培養(yǎng)物進(jìn)行血清學(xué)鑒定,。本試劑盒僅供科研使用。
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
進(jìn)口流感嗜血桿菌凝集抗血清E群檢測(cè)
進(jìn)口流感嗜血桿菌凝集抗血清E群檢測(cè)
進(jìn)口流感嗜血桿菌凝集抗血清F群檢測(cè)
進(jìn)口流感嗜血桿菌凝集抗血清F群檢測(cè)
流感嗜血桿菌血清型A鑒定
流感嗜血桿菌血清型A鑒定
流感嗜血桿菌診斷血清(6種血清型價(jià)格)
【流感嗜血桿菌相關(guān)知識(shí)】
流感嗜血桿菌分類為兩類,,即莢膜菌株及沒(méi)有莢膜的菌株。雖然已知莢膜類的乙型流感嗜血桿菌(或是b型流感嗜血桿菌,,簡(jiǎn)稱HiB)是毒性的主因之一,,但感染流感嗜血桿菌的病因卻仍未*清楚。它們的莢膜能幫助它們抵抗在沒(méi)有免疫的寄主體內(nèi)的吞噬作用及不觸發(fā)補(bǔ)體介導(dǎo)的裂解,。沒(méi)有莢膜的菌株則較少侵略性,,但它們能誘發(fā)炎癥而產(chǎn)生其他病癥,如會(huì)厭炎,。
我司還提供其它進(jìn)口或國(guó)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(chóng)病,、違禁品濫用,、肺炎球菌、軍團(tuán)菌,、化妝品檢測(cè),、食品安全檢測(cè)等試劑盒以及日本生研細(xì)菌分型診斷血清、德國(guó)SiFin診斷血清、丹麥SSI診斷血清等產(chǎn)品,。
( MOB:楊永漢)
想了解更多的產(chǎn)品及服務(wù)請(qǐng)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(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
在顯微鏡下檢查糞便粘液,,并檢查大量膿細(xì)胞。如果使用革蘭氏染色,,則通過(guò)顯微鏡觀察大量的革蘭氏陽(yáng)性球菌,。在糞便中培養(yǎng)金黃色葡萄球菌的生長(zhǎng)并且可以確認(rèn)診斷。球菌測(cè)試首先,,無(wú)菌處理金黃色葡萄球菌的測(cè)試樣品:將25g或25mL食物樣品無(wú)菌取出并置于225mL無(wú)菌生理鹽水溶液中以制備10-1稀釋液,。富集培養(yǎng):將10-1稀釋液加入到7.5%NaCl肉湯或胰蛋白胨肉湯中,并在37℃下培養(yǎng)24小時(shí),。分離和培養(yǎng):將上述稀釋液或培養(yǎng)物在血板和Baird-Parker平板上劃線,,并在37℃下培養(yǎng)24至48小時(shí)。金黃色葡萄球菌是血板上的金黃色或白色菌落,,大而凸,,表面光滑,周圍溶血環(huán),。 Baird-Parker板上的菌落為圓形,,直徑2至3mm,灰色或黑色,,并被混濁區(qū)包圍,。染色觀察:從平板上挑出可疑的菌落并用革蘭氏染色。金黃色葡萄球菌是革蘭氏陽(yáng)性菌,。顯微鏡排列成葡萄狀,,沒(méi)有孢子和蛻膜。直徑為0.5-1μm,。血漿凝固酶試驗(yàn):移取0.5 mL家兔血漿和0.5 mL金黃色葡萄球菌試液輸液肉湯24小時(shí)培養(yǎng)液混勻,,置36±1°C培養(yǎng),每半小時(shí)觀察一次,,連續(xù)觀察6小時(shí)發(fā)生凝固,。當(dāng)小試管傾斜或倒置時(shí),內(nèi)容物不流動(dòng)并被判斷為正面,。同時(shí)作為一個(gè)積極的控制,。
The stool mucus was smeared and a large number of pus cells were examined under a microscope. If Gram stain was used, a large number of Gram-positive cocci were observed by microscopy. The growth of Staphylococcus aureus is c*ted in the stool and the diagnosis can be confirmed. Cocci test First, the test sample of Staphylococcus aureus was treated aseptically: 25 g or 25 mL of food sample was taken aseptically and placed in 225 mL of sterile physiological saline solution to make a 10-1 dilution. Enrichment culture: The 10-1 dilution was added to 7.5% NaCl broth or tryptone broth and incubated at 37°C for 24 hours. Isolation and culture: The above dilutions or cultures were streaked on blood plates and Baird-Parker plates, and cultured at 37°C for 24 to 48 hours. Staphylococcus aureus is golden or white colony on the blood plate, large and convex, smooth surface, surrounded by hemolytic rings. The colonies on the Baird-Parker plate were round, 2 to 3 mm in diameter, gray or black in color and surrounded by a turbid zone. Staining observation: Suspected colonies were picked from the plate and stained with Gram. Staphylococcus aureus was Gram-positive. The microscope was arranged in a grape-like arrangement without spores and decidua. The diameter was 0.5-1 μm. Plasma coagulase test: Pipette 0.5 mL of rabbit plasma and 0.5 mL of Staphylococcus aureus test liquid infusion broth 24-hour culture mix thoroughly, set 36 ± 1 °C culture, observe once every half hour, continuous observation for 6 hours Solidification occurs. When the small test tube is tilted or inverted, the contents do not flow and are judged to be positive. At the same time as a positive control.