ELISA Kit for Immunoglobulin G1 (IgG1)

IGHG1; Ig Gamma-1 Chain C Region; Immunoglobulin Heavy Constant Gamma 1; G1m Marker; Immunoglobulin Gm1

  • ELISA Kit for Immunoglobulin G1 (IgG1) Packages (Simulation)
  • ELISA Kit for Immunoglobulin G1 (IgG1) Packages (Simulation)
  • ELISA Kit for Immunoglobulin G1 (IgG1) Results demonstration
  • CEA074Bo.jpg Typical Standard Curve
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Specificity of the ELISA Kit for Immunoglobulin G1 (IgG1)

This assay has high sensitivity and excellent specificity for detection of Immunoglobulin G1 (IgG1).
No significant cross-reactivity or interference between Immunoglobulin G1 (IgG1) and analogues was observed.

Recovery of the ELISA Kit for Immunoglobulin G1 (IgG1)

Matrices listed below were spiked with certain level of recombinant Immunoglobulin G1 (IgG1) and the recovery rates were calculated by comparing the measured value to the expected amount of Immunoglobulin G1 (IgG1) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 98-105 102
EDTA plasma(n=5) 89-103 94
heparin plasma(n=5) 79-89 86

Precision of the ELISA Kit for Immunoglobulin G1 (IgG1)

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Immunoglobulin G1 (IgG1) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Immunoglobulin G1 (IgG1) 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 Immunoglobulin G1 (IgG1)

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Immunoglobulin G1 (IgG1) 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) 79-98% 87-101% 78-103% 78-98%
EDTA plasma(n=5) 92-99% 79-102% 92-99% 89-101%
heparin plasma(n=5) 91-103% 93-101% 80-95% 97-104%

Stability of the ELISA Kit for Immunoglobulin G1 (IgG1)

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 Immunoglobulin G1 (IgG1)

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

Test principle of the ELISA Kit for Immunoglobulin G1 (IgG1)

This assay employs the competitive inhibition enzyme immunoassay technique. An antibody specific to Immunoglobulin G1 (IgG1) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between Horseradish Peroxidase (HRP) labeled Immunoglobulin G1 (IgG1) and unlabeled Immunoglobulin G1 (IgG1) (Standards or samples) with the pre-coated antibody specific to Immunoglobulin G1 (IgG1). After incubation the unbound conjugate is washed off. The amount of bound HRP conjugate is reverse proportional to the concentration of Immunoglobulin G1 (IgG1) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Immunoglobulin G1 (IgG1) in the sample.

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