General 4-Hydroxynonenal (4-HNE) ELISA Kit

SKU: orb1146751

特色

描述

The General 4-Hydroxynonenal (4-HNE) ELISA Kit is designed to quantify General 4-Hydroxynonenal (4-HNE) in serum, plasma, cell lysates, cell culture supernates and other biological fluids. The kit has a detection range of 0.63-40 ng/mL and a sensitivity of 0.38 ng/mL.

研究领域

Immunology & Inflammation, Infectious Disease & Virology, Metabolism Research, Signal Transduction

图片与验证

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Item 1 of 1

已测应用

ELISA

应用说明

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with 4-HNE. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to 4-HNE. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of 4-HNE in the samples is then determined by comparing the OD of the samples to the standard curve.

关键属性

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反应性	All
样本类型	serum, plasma, cell lysates, cell culture supernates and other biological fluids
检测类型	Competitive
检测时间	2h
范围	0.63-40 ng/mL
灵敏度	0.38 ng/mL
浓度	40 ng/mL

步骤与表现

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Assay Principle	This kit is based on a competitive ELISA detection method. The microtiter plate is pre-coated with target antigen. During the assay, the target antigen in the sample or standard competes with the immobilized target for binding sites on the biotinylated detection antibody specific to the target antigen. After incubation, excess conjugate and unbound sample or standard are removed by washing. HRP–streptavidin (SABC) is then added to each well and incubated, followed by the addition of TMB substrate solution. The enzymatic reaction is terminated by adding an acidic stop solution, and the color change is measured at 450 nm using a microplate reader. The concentration of the target antigen in the samples is determined by comparison with the standard curve and is inversely proportional to the OD450 value.
Kit Components	1. ELISA Microplate 2. Standards 3. Detection Antibody 4. HRP-Streptavidin Conjugate 5. TMB Substrate 6. Dilution buffers 7. Stop Solution 8. Wash Buffer 9. Plate Sealers 10. Manual
Reagent Preparation	1. Wash Buffer: Prepare the 1X Wash Buffer using distilled water according to the manual. 2. Standard: Perform gradient dilution according to the instructions in the manual. 3. Other Concentrated Reagents: Dilute the concentrated reagents using the Dilution Buffers provided in the kit to 1 X working solutions as instructed in the manual. Always use a clean pipette tip for each different solution.
Assay Procedure	This procedure is for reference only. 1. After the kit equilibrates to room temperature, add standards or samples to each well and incubate. 2. Add biotinylated antibody working solution to each well and incubate. 3. Discard liquid, add wash buffer to each well, wash the plate three times, and blot dry on clean absorbent paper. 4. Add streptavidin-HRP working solution to each well and incubate._x000b_5. Discard liquid, add wash buffer to each well, wash the plate five times, and blot dry on clean absorbent paper. 6. Add TMB substrate solution to each well and incubate in the dark. 7. Add stop solution to each well, mix thoroughly, and immediately read OD at 450 nm.
Materials Required	1. Microplate readers 2. Centrifuge 3. Incubator 4. Automated plate washer 5. Single-channel or multi-channel high-precision pipettes 6. Disposable pipette tips 7. Sterile tubes 8. Eppendorf tubes 9. Absorbent paper 10. Loading slots
Precision	Intra-assay Precision (Precision within an assay): CV% < 8% Intra-assay precision was evaluated by testing multiple replicates of samples within the same plate. Inter-assay Precision (precision between assays): CV% < 10% Inter-assay precision was evaluated by testing samples across different plates.
Calculation of Results	1. Average the duplicate readings for each Standard, Control, and Sample, and subtract the mean optical density of the zero Standard. 2. Construct a standard curve by plotting the target concentration on the y-axis against absorbance on the x-axis and draw a curve through the data points. 3. Determine the sample concentration by substituting the OD450 value into the standard curve. For diluted samples, multiply the calculated value by the corresponding dilution factor.
Curve Fitting Softwares	1. Curve Expert 2. Thermo SkanIt RE 3. SciDAVis 4. LabPlot 5. ……

储存与操作

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储存	请参阅操作手册中的储存说明
有效期	6 months from date of receipt.
免责声明	For research use only

别名

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4-HNE; HNE; 4-hydroxy-2-nonenal; 4-Hydroxynonenal

质量保证

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常用数据库链接

基因符号

4-HNE

实验方案信息