CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC)

CXCL11; I-TAC; IP9; SCYB11; SCYB9B; B-R1; Chemokine(C-X-C-Motif)ligand 11; Small Inducible Cytokine Subfamily B Member 11; Interferon gamma-inducible protein 9

  • CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) Packages (Simulation)
  • CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) Packages (Simulation)
  • CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) Results demonstration
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Specificity of the CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC)

This assay has high sensitivity and excellent specificity for detection of Interferon Inducible T-Cell Alpha Chemoattractant (ITaC).
No significant cross-reactivity or interference between Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) and analogues was observed.

Recovery of the CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC)

Matrices listed below were spiked with certain level of recombinant Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) and the recovery rates were calculated by comparing the measured value to the expected amount of Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 90-97 93
EDTA plasma(n=5) 78-99 89
heparin plasma(n=5) 81-101 97

Precision of the CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC)

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) 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 CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC)

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) 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) 83-101% 94-105% 97-105% 89-104%
EDTA plasma(n=5) 78-92% 92-101% 93-101% 95-102%
heparin plasma(n=5) 79-102% 90-103% 84-101% 79-92%

Stability of the CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC)

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 CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC)

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 100µL Substrate Solution. Incubate 10 minutes at 37°C;
8. Read RLU value immediately.

Test principle of the CLIA Kit for Interferon Inducible T-Cell Alpha Chemoattractant (ITaC)

The microplate provided in this kit has been pre-coated with an antibody specific to Interferon Inducible T-Cell Alpha Chemoattractant (ITaC). Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to Interferon Inducible T-Cell Alpha Chemoattractant (ITaC). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is proportional to the Interferon Inducible T-Cell Alpha Chemoattractant (ITaC) level in the sample or standard.;

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