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ELISA Kit for Anti-Albumin Antibody (AAA)
Serum albumin
Organism species Homo sapiens (Human)
Product No.AEB028Hu
Sample typeSerum, plasma and other biological fluids.
Format96-well strip plate
Assay length4 hours
Detection range3.125-200ng/mL The standard curve concentrations used for the ELISA’s were 200ng/mL, 100ng/mL, 50ng/mL, 25ng/mL, 12.5ng/mL, 6.25ng/mL, 3.125ng/mL
SensitivityThe minimum detectable dose of this kit is typically less than 1.27ng/mL.
This assay has high sensitivity and excellent specificity for detection of Anti-Albumin Antibody (AAA).
No significant cross-reactivity or interference between Anti-Albumin Antibody (AAA) and analogues was observed.
Matrices listed below were spiked with certain level of Anti-Albumin Antibody (AAA) and the recovery rates were calculated by comparing the measured value to the expected amount of Anti-Albumin Antibody (AAA) in samples.
Matrix Recovery range (%) Average(%)
EDTA plasma(n=5)92-10197
heparin plasma(n=5)80-103101
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Anti-Albumin Antibody (AAA) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Anti-Albumin Antibody (AAA) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Anti-Albumin Antibody (AAA) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample 1:2 1:4 1:8 1:16
EDTA plasma(n=5)85-97%95-105%89-102%93-105%
heparin plasma(n=5)87-101%91-101%81-103%90-102%
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
TMB Substrate 1×9mL Stop Solution 1×6mL
Wash Buffer (30 × concentrate) 1×20mL Instruction manual 1
Test principle
The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate solution is added, those wells that contain Anti-Albumin Antibody (AAA) 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 Anti-Albumin Antibody (AAA) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Package and Components
Assay procedure summary
1. Prepare all reagents, samples and
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
4. Aspirate and wash 5 times;
5. Add 90µL Substrate Solution. Incubate 15
    -25 minutes at 37oC;
6. Add 50µL Stop Solution. Read at 450nm
Reagent Preparation
Results demonstration
Typical Standard Curve
Benchmark price
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