產(chǎn)品名稱：大鼠己糖激酶試劑盒 
    產(chǎn)品規(guī)格：96人份/48人份
    ：
    檢測(cè)方法：酶聯(lián)免疫法/酶免法（ELISA）
    96T指可以做94個(gè)標(biāo)本，2個(gè)標(biāo)準(zhǔn)對(duì)照
    48T指可以做47個(gè)標(biāo)本，1個(gè)標(biāo)準(zhǔn)對(duì)照
    96T-84個(gè)樣本
    48T-42個(gè)樣本
    該產(chǎn)品中英文操作步驟以人凝血酶激活纖溶抑制物試劑盒為例：
大鼠己糖激酶試劑盒  操作步驟
    1. 標(biāo)準(zhǔn)品的稀釋與加樣：在酶標(biāo)包被板上設(shè)標(biāo)準(zhǔn)品孔10孔，在*、第二孔中分別加標(biāo)準(zhǔn)品100μl，然后在*、第二孔中加標(biāo)準(zhǔn)品稀釋液50μl，混勻；然 后從*孔、第二孔中各取100μl分別加到第三孔和第四孔，再在第三、第四孔分別加標(biāo)準(zhǔn)品稀釋液50μl，混勻；然后在第三孔和第四孔中先各取50μl 棄掉，再各取50μl分別加到第五、第六孔中，再在第五、第六孔中分別加標(biāo)準(zhǔn)品稀釋液50ul，混勻；混勻后從第五、第六孔中各取50μl分別加到第七、 第八孔中，再在第七、第八孔中分別加標(biāo)準(zhǔn)品稀釋液50μl，混勻后從第七、第八孔中分別取50μl加到第九、第十孔中，再在第九第十孔分別加標(biāo)準(zhǔn)品稀釋液 50μl，混勻后從第九第十孔中各取50μl棄掉。（稀釋后各孔加樣量都為50μl，濃度分別為6μg/ml，4μg/ml ，2μg/ml，1μg/ml ， 0.5μg/ml）。
    2.加樣：分別設(shè)空白孔（空白對(duì)照孔不加樣品及酶標(biāo)試劑，其余各步操作相同）、待測(cè)樣品孔。在酶標(biāo)包被板上待測(cè)樣品孔中先加樣品稀釋液40μl，然后再加待測(cè)樣品10μl（樣品zui終稀釋度為5倍）。加樣將樣品加于酶標(biāo)板孔底部，盡量不觸及孔壁，輕輕晃動(dòng)混勻。
    3.溫育：用封板膜封板后置37℃溫育30分鐘。
    4.配液：將30（48T的20倍）倍濃縮洗滌液用蒸餾水30（48T的20倍）倍稀釋后備用。
    5.洗滌：小心揭掉封板膜，棄去液體，甩干，每孔加滿洗滌液，靜置30秒后棄去，如此重復(fù)5次，拍干。
    6.加酶：每孔加入酶標(biāo)試劑50μl，空白孔除外。
    7.溫育：操作同3。
    8.洗滌：操作同5。
    9.顯色：每孔先加入顯色劑A50μl，再加入顯色劑B50μl，輕輕震蕩混勻，37℃避光顯色15分鐘.
    10.終止：每孔加終止液50μl，終止反應(yīng)（此時(shí)藍(lán)色立轉(zhuǎn)黃色）。
    11.測(cè)定：以空白空調(diào)零，450nm波長(zhǎng)依序測(cè)量各孔的吸光度（OD值）。 測(cè)定應(yīng)在加終止液后15分鐘以內(nèi)進(jìn)行。
    Assay procedure
    1.Dilute and add sample to Standard: set 10 Standard wells on the ELISA plates coated, add Standard 100μl to the first and the second well, then add Standard dilution 50μl to the first and the second well, mix; take out 100μl form the first and the second well then add it to the third and the forth well separay. then add Standard dilution 50μl to the third and the forth well ,mix ; then take out 50μl from the third and the forth well discard, add 50μl to the fifth and the sixth well ,then add Standard dilution 50μl to the fifth and the sixth well, mix ; take out 50μl from the fifth and the sixth well and add to the seventh and the eighth well, then add Standard dilution 50μl to the seventh and the eighth well ,mix ; take out 50μl from the seventh and the eighth well and add to the ninth and the tenth well, add Standard dilution 50μl to the ninth and the tenth well, mix , take out 50μl from the ninth and the tenth well discard（add Sample 50μl to each well after Diluting ,（density: 6μg/ml，4μg/ml ，2μg/ml，1μg/ml ， 0.5μg/ml）
    2.add sample：Set blank wells separay （blank comparison wells don’t add sample and HRP-Conjugate reagent, other each step operation is same）. testing sample well. add Sample dilution 40μl to testing sample well, then add testing sample 10μl （sample final dilution is 5-fold）, add sample to wells , don’t touch the well wall as far as possible, and Gently mix.
    3.Incubate: After closing plate with Closure plate membrane ,incubate for 30 min at 37℃.
    4.Configurate liquid: 30-fold （or 20-fold）wash solution diluted 30-fold （or 20-fold） with distilled water and reserve.
    5.washing：Uncover Closure plate membrane, discard Liquid, dry by swing, add washing buffer to every well, still for 30s then drain, repeat 5 times, dry by pat.
    6.add enzyme：Add HRP-Conjugate reagent 50μl to each well, except blank well.
    7.incubate：Operation with 3.
    8.washing：Operation with 5.
    9.color：Add Chromogen Solution A 50ul and Chromogen Solution B to each well, evade the light preservation for 15 min at 37℃
    10.Stop the reaction：Add Stop Solution50μl to each well, Stop the reaction（the blue color change to yellow color）.
    11.assay：take blank well as zero , Read absorbance at 450nm after Adding Stop Solution and within 15min.
大鼠己糖激酶試劑盒  范圍: 人,小大鼠,豬,兔,其它動(dòng)物細(xì)胞因子;細(xì)胞凋亡,活性多肽,自身抗體 ,血栓與止血, 骨代謝,肝纖維化,腫瘤,激素內(nèi)分泌,自身抗體科研ELISA檢測(cè)試劑盒。