Elisa kit for IL-6

Our Elisa Kit products are perfect for the analysis of biological fluids, including Serum, plasma, tissue homogenates, cell lysates, cell culture supernatants, and other biological fluids.

This Elisa Kit assay has high sensitivity and excellent specificity for the detection of Interleukin 6 (IL6). ConductScience offers Elisa Kits for Analysis.

$690.00

Specificity

This assay has high sensitivity and excellent specificity for the detection of Interleukin 6 (IL6).
No significant cross-reactivity or interference between Interleukin 6 (IL6) and analogs was observed.

Recovery

Matrices listed below were spiked with a certain levels of recombinant Interleukin 6 (IL6) and the recovery rates were calculated by comparing the measured value to the expected amount of Interleukin 6 (IL6) in samples.

MatrixRecovery range (%)Average(%)
serum(n=5)84-9789
EDTA plasma(n=5)92-10297
heparin plasma(n=5)85-9893

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high-level Interleukin 6 (IL6) were tested 20 times on one plate, respectively. 
Inter-assay Precision (Precision between assays): 3 samples with low, middle, and high-level Interleukin 6 (IL6) were tested on 3 different plates, with 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 Interleukin 6 (IL6) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample1:21:41:81:16
serum(n=5)78-102%97-104%93-101%96-105%
EDTA plasma(n=5)99-105%89-98%93-101%95-102%
heparin plasma(n=5)99-105%95-103%87-103%78-103%

Stability

The stability of the 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 conditions. 
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, and 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

Sample1:21:41:81:16
serum(n=5)78-102%97-104%93-101%96-105%
EDTA plasma(n=5)99-105%89-98%93-101%95-102%
heparin plasma(n=5)99-105%95-103%87-103%78-103%

Procedure

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

Additional information

Brand

Cloud Clone

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