人內(nèi)皮脂肪酶(EL/LIPG)ELISA檢測(cè)試劑盒子科生物現(xiàn)貨供應(yīng),子科生物進(jìn)口elisa試劑盒,國(guó)產(chǎn)elisa試劑盒,elisa試劑盒說(shuō)明書(shū),elisa試劑盒免費(fèi)代測(cè),ELISA試劑盒技術(shù)服務(wù),如需Elisa試劑盒說(shuō)明書(shū)及報(bào)價(jià),可我司。
人內(nèi)皮脂肪酶(EL/LIPG)ELISA檢測(cè)試劑盒
?產(chǎn)品規(guī)格:96T(人份)/48T(人份)(單孔檢測(cè)分別可以檢測(cè)90份樣本,42分樣本,一般都需要留6個(gè)孔做標(biāo)準(zhǔn)曲線)。
?標(biāo)本:血清、血漿、細(xì)胞上清液、尿液、體液、灌洗液、腦脊髓、心房水、胸房水、組織等
?運(yùn)輸:全國(guó)各地快遞免費(fèi)送貨上門(mén),低溫運(yùn)輸,用冰袋加泡沫保溫盒包裝,確保產(chǎn)品運(yùn)輸狀態(tài)下也處于低溫狀態(tài)。
人內(nèi)皮脂肪酶(EL/LIPG)ELISA檢測(cè)試劑盒試劑的準(zhǔn)備:
1. 標(biāo)準(zhǔn)品:標(biāo)準(zhǔn)品的系列稀釋?xiě)?yīng)在實(shí)驗(yàn)時(shí)準(zhǔn)備,不能儲(chǔ)存。稀釋前將標(biāo)準(zhǔn)品振蕩混勻。稀釋比例按下表中進(jìn)行:
500pg/ml(6號(hào)標(biāo)準(zhǔn)品) 原倍濃度不用稀釋直接加入50ul
250pg/ml(5號(hào)標(biāo)準(zhǔn)品) 100ul的原倍標(biāo)準(zhǔn)品加入100ul的標(biāo)準(zhǔn)品稀釋液
125pg/ml(4號(hào)標(biāo)準(zhǔn)品) 100ul的5號(hào)標(biāo)準(zhǔn)品加入100ul的標(biāo)準(zhǔn)品稀釋液
62.5pg/ml(3號(hào)標(biāo)準(zhǔn)品) 100ul的4號(hào)標(biāo)準(zhǔn)品加入100ul的標(biāo)準(zhǔn)品稀釋液
31.2pg/ml(2號(hào)標(biāo)準(zhǔn)品) 100ul的3號(hào)標(biāo)準(zhǔn)品加入100ul的標(biāo)準(zhǔn)品稀釋液
15.6pg/ml(1號(hào)標(biāo)準(zhǔn)品) 100ul的2號(hào)標(biāo)準(zhǔn)品加入100ul的標(biāo)準(zhǔn)品稀釋液
0pg/ml (空白對(duì)照) 原倍濃度不用稀釋直接加入50ul
2. 洗滌緩沖液(50×)的稀釋:蒸餾水50倍稀釋。
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。稀釋度的線性。樣品線性回歸與預(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%。
Assay procedure
1. Prepare all reagents before starting assay procedure. It is recommended that all Standards and Samples be added in duplicate to the Microelisa Stripplate.
2. Add standard: Set Standard wells, testing sample wells. Add standard 50μl to standard well.
3. Add Sample: Add testing sample 10μl then add Sample Diluent 40μl to testing sample well; Blank well doesn’t add anyting.
4. Add 100μl of HRP-conjugate reagent to each well, cover with an adhesive strip and incubate for 60 minutes at 37°C.
5. Aspirate each well and wash, repeating the process four times for a total of five washes. Wash by filling each well with Wash Solution (400μl) using a squirt bottle, manifold dispenser or autowasher. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Solution by aspirating or decanting. Invert the plate and blot it against clean paper towels.
6. Add chromogen solution A 50μl and chromogen solution B 50μl to each well. Gently mix and incubate for 15 minutes at 37°C. Protect from light.
7. Add 50μl Stop Solution to each well. The color in the wells should change from blue to yellow. If the color in the wells is green or the color change does not
appear uniform, gently tap the plate to ensure thorough mixing.
8. Read the Optical Density (O.D.) at 450 nm using a microtiter plate reader within 15 minutes.
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