花生四烯酸-5-脂加氧酶(ALOX5)检测试剂盒

花生四烯酸-5-脂加氧酶(ALOX5)检测试剂盒

适用生物     Homo sapiens (Human，人)    

花生四烯酸-5-脂加氧酶(ALOX5)检测试剂盒   

检测范围     0.156-10ng/mL     灵敏度     0.053ng/mL    

样本类型     Tissue homogenates, cell lysates and other biological fluids.    

实验时长     4.5h     实验方法     双抗夹心法     花生四烯酸-5-脂加氧酶(ALOX5)检测试剂盒   

规格     96T    

ELISA Kit for Arachidonate-5-Lipoxygenase (ALOX5)

FOR IN VITRO AND RESEARCH USE ONLY, NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES!

Organism species     Homo sapiens (Human)    

花生四烯酸-5-脂加氧酶(ALOX5)检测试剂盒  

Sample type     Tissue homogenates, cell lysates and other biological fluids.    

Format     96-well strip plate    

Assay length     4.5 hours    

Detection range     0.156-10ng/mL The standard curve concentrations used for the ELISA’s were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL    

Sensitivity     The minimum detectable dose of this kit is typically less than 0.053ng/mL.    

Specificity

This assay has high sensitivity and excellent specificity for detection of Arachidonate-5-Lipoxygenase (ALOX5).
No significant cross-reactivity or interference between Arachidonate-5-Lipoxygenase (ALOX5) and analogues was observed.

花生四烯酸-5-脂加氧酶(ALOX5)检测试剂盒Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Arachidonate-5-Lipoxygenase (ALOX5) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Arachidonate-5-Lipoxygenase (ALOX5) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Stability

The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

Reagents and materials provided

Reagents     Quantity     Reagents     Quantity    

Pre-coated, ready to use 96-well strip plate     1     Plate sealer for 96 wells     4    

Standard     2     Standard Diluent     1×20mL    

Detection Reagent A     1×120μL     Assay Diluent A     1×12mL    

Detection Reagent B     1×120μL     Assay Diluent B     1×12mL    

TMB Substrate     1×9mL     Stop Solution     1×6mL    

Wash Buffer (30 × concentrate)     1×20mL     Instruction manual     1    

Assay procedure summary

1. Prepare all reagents, samples and standards;
2. Add 100μL standard or sample to each well. Incubate 2 hours at 37oC;
3. Aspirate and add 100μL prepared Detection Reagent A. Incubate 1 hour at 37oC;
4. Aspirate and wash 3 times;
5. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37oC;
6. Aspirate and wash 5 times;
7. Add 90μL Substrate Solution. Incubate 15-25 minutes at 37oC;
8. Add 50μL Stop Solution. Read at 450nm immediately.

花生四烯酸-5-脂加氧酶(ALOX5)检测试剂盒Test principle

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Arachidonate-5-Lipoxygenase (ALOX5). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Arachidonate-5-Lipoxygenase (ALOX5). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Arachidonate-5-Lipoxygenase (ALOX5), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Arachidonate-5-Lipoxygenase (ALOX5) in the samples is then determined by comparing the O.D. of the samples to the standard curve.