鸡透明质酸（HA）ELISA试剂盒 返回列表页

●产品名称：鸡透明质酸（HA）ELISA试剂盒，鸡透明质酸（HA）酶联免疫试剂盒，鸡透明质酸（HA）ELISA试剂盒说明书，深圳子科生物ELISA试剂盒暑期5折*
●英文名称：Chicken Hyaluronic acid,HA ELISA Kit
●货号：ZK-C6308
●规格： 96T/48T
●品牌：子科生物ZIKER
●反应时间： 1-5h
●所需样本体积： 50-100ul
●检测波长： 450 nm
●用途： For research use only. Not for diagnostic use.
●特点：灵敏性高、特异性强、重复性好
●服务：子科生物所有的elisa试剂盒均可免费代测，全程Elisa实验技术指导。
●运输：全国各地快递免费送货上门，低温运输，用冰袋加泡沫保温盒包装，确保产品运输状态下也处于低温状态。

ELISA试剂盒检测方法：双抗体夹心法、双抗原夹心法、间接法测抗体、双位点一步法、 竞争法 、捕获法、ABS-ELISA方法，我们子科生物主要采用双抗体夹心法。详细可以咨询我们销售人员。

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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