ELISA Kit for Anti-Albumin Antibody (AAA)

Serum albumin
Typical Standard Curve Typical Standard Curve

Sample type Serum, plasma and other biological fluids. Detection range 3.125-200ng/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
Sensitivity The minimum detectable dose of this kit is typically less than 1.27ng/mL. Specificity 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.

Recovery 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

Precision 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%

Linearity 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%

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.
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. Assay procedure summary 1. Prepare all reagents, samples and standards;
Reagent Preparation
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 5 times;
5. Add 90µL Substrate Solution. Incubate 15-25 minutes at 37oC;
6. Add 50µL Stop Solution. Read at 450nm immediately.

Reagents and materials provided
  • Pre-coated, ready to use 96-well strip plate1
  • Plate sealer for 96 wells4
  • Standard2
  • Standard Diluent1×20mL
  • Detection Reagent A1×120µL
  • Assay Diluent A1×12mL
  • TMB Substrate1×9mL
  • Stop Solution1×6mL
  • Wash Buffer (30 × concentrate)1×20mL
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