人伴侶蛋白10（CPN10）ELISA檢測試劑盒

●規(guī)格： 96T/48T
●反應時間： 1-5h
●所需樣本體積： 50-100ul
●檢測波長： 450 nm
●用途： For research use only. Not for diagnostic use.
●特點：靈敏性高、特異性強、重復性好
●服務：子科生物所有的elisa試劑盒均可免費代測，全程Elisa實驗技術指導。

深圳子科生物ELISA試劑盒優(yōu)質供應商，擁有10年的研發(fā)和生產經驗，擁有*的儀器設備，專業(yè)的技術人員和*的實驗技術，目前已經建立強大的實驗技術服務平臺，品牌設立為：ZIKER 。產品詳細報價可以咨詢我們公司客服人員，：

人伴侶蛋白10（CPN10）ELISA檢測試劑盒

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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