人肌抑素(MSTN)ELISA檢測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)定性強的自產(chǎn)國產(chǎn)人ELISA試劑盒,大鼠ELISA試劑盒,小鼠ELISA試劑盒,魚ELISA試劑盒,植物ELISA試劑盒,牛羊豬雞ELISA試劑盒性價比*。咨詢!
人肌抑素(MSTN)ELISA檢測試劑盒?檢測方法:酶聯(lián)免疫分析ELISA方法
?有效期: 4 個月(4℃);8 個月(-20℃)。 ?保存方法: 2-8℃(頻繁使用時); -20℃(長時間不用時)。 ?品牌:子科生物ZIKER,美國R&D,美國immonoway,美國sciencell,德國IBL,
?質(zhì)量保證:我告訴所有產(chǎn)品均需要經(jīng)過質(zhì)檢通過后,才允許出庫!?適用范圍:實驗結(jié)果僅供科研參考,不推薦用于臨床診斷結(jié)果。?ELISA常用的方法:雙抗體夾心法、間接法、競爭法以及BAS-ELISA等,子科生物ELISA產(chǎn)品主要用雙抗體夾心法。?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?產(chǎn)品性能:靈敏度高,特異性強,重復(fù)性。
人肌抑素(MSTN)ELISA檢測試劑盒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.
Calculation of results
1.This standard curve is used to determine the amount in an unknown sample. The standard curve is generated by plotting the average O.D. (450 nm) obtained for each of the six standard concentrations on the vertical (Y) axis versus the corresponding concentration on the horizontal (X) axis.
2.First, calculate the mean O.D. value for each standard and sample. All O.D. values, are subtracted by the mean value of the zero standard before result interpretation. Construct the standard curve using graph paper or statistical software.
3.To determine the amount in each sample, first locate the O.D. value on the Y-axis and extend a horizontal line to the standard curve. At the point of intersection, draw a vertical line to the X-axis and read the corresponding concentration.
4.Any variation in operator, pipetting and washing technique, incubation time or temperature, and kit age can cause variation in result. Each user should obtain their own standard curve.
5.The sensitivity by this assay is 10.0 pg/ml
6.Standard curve
Storage: 2-8℃.
validity: six months.
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