Monkey GNRH ELISA Kit

SKU: orb566453

特色

描述

Monkey GNRH (Gonadotropin-releasing hormone) ELISA Kit

研究领域

Signal Transduction, Stem Cell & Developmental Biology

图片与验证

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Item 1 of 1

关键属性

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反应性	Monkey
样本类型	Serum,Plasma,Cell Culture Supernatant,Cell or tissue lysate,Other liquid samples
检测类型	Competitive
检测时间	2 hours
范围	15.625-1000nmol/ml
灵敏度	9.375nmol/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	2 - 8 °C for 12 months
有效期	6 months from date of receipt.
免责声明	For research use only

别名

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质量保证

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常用数据库链接

基因符号

GNRH

UniProt

A0A2K5VL54

UniProt 详情

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暂无 UniProt 数据

实验方案信息

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