ELISA Kit for Fc Fragment Of IgA Receptor (FcaR)

CD89; FcaRI; Receptor I For The Fc Region Of Immunoglobulin A; IgA Fc receptor; Immunoglobulin alpha Fc receptor

  • ELISA Kit for Fc Fragment Of IgA Receptor (FcaR) Packages (Simulation)
  • ELISA Kit for Fc Fragment Of IgA Receptor (FcaR) Packages (Simulation)
  • ELISA Kit for Fc Fragment Of IgA Receptor (FcaR) Results demonstration
  • SEB402Hu.jpg Typical Standard Curve
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Specificity of the ELISA Kit for Fc Fragment Of IgA Receptor (FcaR)

This assay has high sensitivity and excellent specificity for detection of Fc Fragment Of IgA Receptor (FcaR).
No significant cross-reactivity or interference between Fc Fragment Of IgA Receptor (FcaR) and analogues was observed.

Recovery of the ELISA Kit for Fc Fragment Of IgA Receptor (FcaR)

Matrices listed below were spiked with certain level of recombinant Fc Fragment Of IgA Receptor (FcaR) and the recovery rates were calculated by comparing the measured value to the expected amount of Fc Fragment Of IgA Receptor (FcaR) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 95-104 98
EDTA plasma(n=5) 86-103 98
heparin plasma(n=5) 78-90 86

Precision of the ELISA Kit for Fc Fragment Of IgA Receptor (FcaR)

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

Linearity of the ELISA Kit for Fc Fragment Of IgA Receptor (FcaR)

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Fc Fragment Of IgA Receptor (FcaR) 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
serum(n=5) 85-96% 90-98% 96-104% 95-104%
EDTA plasma(n=5) 81-101% 81-99% 82-101% 85-99%
heparin plasma(n=5) 80-105% 91-99% 90-102% 92-103%

Stability of the ELISA Kit for Fc Fragment Of IgA Receptor (FcaR)

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.

Assay procedure summary of the ELISA Kit for Fc Fragment Of IgA Receptor (FcaR)

1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
8. Add 50µL Stop Solution. Read at 450nm immediately.

Test principle of the ELISA Kit for Fc Fragment Of IgA Receptor (FcaR)

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 Fc Fragment Of IgA Receptor (FcaR). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Fc Fragment Of IgA Receptor (FcaR). 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 Fc Fragment Of IgA Receptor (FcaR), 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 Fc Fragment Of IgA Receptor (FcaR) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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