甲型流感病毒抗原診斷試劑（美國OSOM）

廣州健侖生物科技有限公司

廣州健侖長期供應(yīng)各種流感檢測試劑，包括進口和國產(chǎn)的品牌，主要包括日本富士瑞必歐、日本生研、美國BD、美國NovaBios、美國binaxNOW、日本積水、日本榮研、美國OSOM、芬蘭、愛思普林、英國Clearview、凱必利、廣州創(chuàng)侖等主流品牌。

甲型流感病毒抗原診斷試劑（美國OSOM）

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【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  】 2042552662
【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室

對照/標(biāo)本無染色
① 確認是否忽略了應(yīng)該加的某種試劑，包括一抗、二抗、三抗及底物等。
② 確認所有的試劑是否按正確的順序加入，是否孵育了足夠的時間。
③ 對照抗體的標(biāo)簽確認是否使用了正確的抗體，以及所用的檢測系統(tǒng)是否和一抗匹配，這一點是非常重要的。比如，如果一抗是兔來源的抗體，二抗一定要用抗兔的二抗來匹配；或一抗是小鼠的IgM 一抗，二抗必須是山羊/兔抗小鼠的IgM（不是IgG）二抗。
④ 檢查抗體所使用的稀釋度及稀釋溶液。
⑤ 檢查抗體的有效期和保存條件，尤其是標(biāo)記了酶或熒光素的抗體，現(xiàn)在大多數(shù)試劑公司的抗體均要求在4~8℃條件下保存，應(yīng)避免反復(fù)凍融，試劑保存時一定要避免與揮發(fā)性有機溶劑同放一室，以免降低抗體的效價。
⑥ 檢查標(biāo)本的儲存條件，用已知陽性的標(biāo)本來同時做陽性對照。
⑦ 檢查色原/底物溶液，zui簡單的檢測方法是將一滴標(biāo)記有酶的抗體加入到制備好的底物溶液中，如果底物發(fā)生預(yù)期的顏色變化，則可排除底物的因素。需要注意的是，有些底物在制成工作液后應(yīng)在一定時間內(nèi)用完，否則會失效。
⑧ 檢查沖洗液是否和反應(yīng)試劑匹配，溶液的pH 值很重要，與過氧化物酶底物匹配的溶液中不應(yīng)含有疊氮鈉。
⑨ 檢查復(fù)染劑和封片劑是否和所使用的色原匹配。

Control / specimen no staining
① Confirm whether to ignore some reagents should be added, including the first antibody, the second antibody, the third antibody and substrate.
② Confirm that all reagents are added in the correct order, and incubate enough time.
It is important that the control antibody label confirm that the correct antibody is being used and whether the detection system used matches the primary antibody. For example, if the primary antibody is a rabbit-derived antibody, the secondary antibody must be matched with the secondary antibody to the rabbit; or the primary antibody is the IgM primary antibody of the mouse and the secondary antibody must be a goat / rabbit anti-mouse IgM )Secondary Antibodies.
④ check the antibody used in the dilution and dilution solution.
⑤ check the validity of the antibody and storage conditions, especially labeled with enzyme or fluorescein antibody, and now most of the reagents companies require storage at 4 ~ 8 ℃ conditions, should be avoided repeated freezing and thawing, reagent preservation must be avoided And volatile organic solvents with a room, so as not to reduce the antibody titer.
⑥ check the specimen storage conditions, it is best to use known positive specimens to do positive control at the same time.
⑦ check the chromogen / substrate solution, the simplest detection method is to add a drop of enzyme labeled antibody added to the prepared substrate solution, if the substrate expected color change, you can rule out the substrate factor. It should be noted that some substrates should be used within a certain period of time after they are made into the working solution, otherwise they will fail.
⑧ Check whether the rinse solution and the reaction reagent match, the pH value of the solution is very important, and peroxidase substrate solution should not contain sodium azide.
⑨ check counterstain and packing agent and the color of the original match.