人β葡萄糖醛酸苷酶(βGD)ELISA檢測(cè)試劑盒子科生物研發(fā)生產(chǎn)現(xiàn)貨供應(yīng),深圳子科生物提供大量品牌進(jìn)口原裝,分裝,以及穩(wěn)定性強(qiáng)的自產(chǎn)國(guó)產(chǎn)人ELISA試劑盒,大鼠ELISA試劑盒,小鼠ELISA試劑盒,魚(yú)ELISA試劑盒,植物ELISA試劑盒,牛羊豬雞ELISA試劑盒性?xún)r(jià)比*。咨詢(xún)!
人β葡萄糖醛酸苷酶(βGD)ELISA檢測(cè)試劑盒
●產(chǎn)品規(guī)格:96T(人份)/48T(人份)
單孔檢測(cè):96T,可以檢測(cè)90份樣本,留5個(gè)孔做標(biāo)準(zhǔn)曲線(xiàn),一個(gè)孔做空白對(duì)照;
48T,可以檢測(cè)42份樣本,留5個(gè)孔做標(biāo)準(zhǔn)曲線(xiàn),一個(gè)孔做空白對(duì)照;
●品牌:子科生物ZIKER,美國(guó)R&D,美國(guó)immonoway,美國(guó)sciencell,德國(guó)IBL
●適用范圍:實(shí)驗(yàn)結(jié)果僅供科研參考,不推薦用于臨床診斷結(jié)果。
人β葡萄糖醛酸苷酶(βGD)ELISA檢測(cè)試劑盒樣品收集、處理及保存方法:
1、 血清……操作過(guò)程中避免任何細(xì)胞刺激。使用不含熱原和內(nèi)毒素的試管。收集血液后,1000×g離心10分鐘將血紅細(xì)胞迅速小心地分離。
2、 血漿……EDTA、檸檬酸鹽、肝素血漿可用于檢測(cè)。1000×g離心30分鐘去除顆粒。
3、 細(xì)胞上清液……1000×g離心10分鐘去除顆粒和聚合物。
4、 組織勻漿……將組織加入適量理鹽水搗碎。1000×g離心10分鐘,取上清液。
5、 保存……如果樣品不立即使用,應(yīng)將其分成小部分-70℃保存,避免反復(fù)冷凍。盡可能的不要使用溶血或高血脂血。如果血清中大量顆粒,檢測(cè)前先離心或過(guò)濾。不要在37℃或更高的溫度加熱解凍。應(yīng)在室溫下解凍并確保樣品均勻地充分解凍。
人β葡萄糖醛酸苷酶(βGD)ELISA檢測(cè)試劑盒試劑盒性能:
1. 靈敏度:zui小的檢測(cè)濃度小于1號(hào)標(biāo)準(zhǔn)品。稀釋度的線(xiàn)性。樣品線(xiàn)性回歸與預(yù)期濃度相關(guān)系數(shù)R值為0.990。
2. 特異性:不與其它細(xì)胞因子反應(yīng)。
3. 重復(fù)性:板內(nèi)、板間變異系數(shù)均小于10%。
人β葡萄糖醛酸苷酶(βGD)ELISA檢測(cè)試劑盒操作步驟:
1. 使用前,將所有試劑充分混勻。不要使液體產(chǎn)生大量的泡沫,以免加樣時(shí)加入大量的氣泡,產(chǎn)生加樣上的誤差。
2. 根據(jù)待測(cè)樣品數(shù)量加上標(biāo)準(zhǔn)品的數(shù)量決定所需的板條數(shù)。每個(gè)標(biāo)準(zhǔn)品和空白孔建議做復(fù)孔。每個(gè)樣品根據(jù)自己的數(shù)量來(lái)定,能使用復(fù)孔的盡量做復(fù)孔。
3. 加入稀釋好后的標(biāo)準(zhǔn)品50ul于反應(yīng)孔、加入待測(cè)樣品50ul于反應(yīng)孔內(nèi)。立即加入50ul的生物素標(biāo)記的抗體。蓋上膜板,輕輕振蕩混勻,37℃溫育45分鐘。
4. 甩去孔內(nèi)液體,每孔加滿(mǎn)洗滌液,振蕩30秒,甩去洗滌液,用吸水紙拍干。重復(fù)此操作4次。如果用洗板機(jī)洗滌,洗滌次數(shù)增加一次。
5. 每孔加入100ul的親和鏈酶素-HRP,輕輕振蕩混勻,37℃溫育30分鐘。
6. 甩去孔內(nèi)液體,每孔加滿(mǎn)洗滌液,振蕩30秒,甩去洗滌液,用吸水紙拍干。重復(fù)此操作4次。如果用洗板機(jī)洗滌,洗滌次數(shù)增加一次。
7. 每孔加入底物A、B各50ul,輕輕振蕩混勻,37℃溫育5分鐘。避免光照。
8. 取出酶標(biāo)板,迅速加入50ul終止液,加入終止液后應(yīng)立即測(cè)定結(jié)果。
9. 在450nm波長(zhǎng)處測(cè)定各孔的OD值。
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