CLIA Kit for Enolase 1 (ENO1)

NNE; ENO1L1; MPB1; PPH; Alpha Enolase; Enolase 1; Phosphopyruvate hydratase; Plasminogen-binding protein; 2-phospho-D-glycerate hydro-lyase; C-myc promoter-binding

The microplate provided in this kit has been pre-coated with an antibody specific to Enolase 1 (ENO1) . Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to Enolase 1 (ENO1) . 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 Enolase 1 (ENO1) level in the sample or standard.

1. Prepare all reagents, samples and standards; <br/> 2. Add 100&micro; L standard or sample to each well. Incubate 2 hours at 37&deg; C; <br/> 3. Aspirate and add 100&micro; L prepared Detection Reagent A. Incubate 1 hour at 37&deg; C; <br/> 4. Aspirate and wash 3 times; <br/> 5. Add 100&micro; L prepared Detection Reagent B. Incubate 30 minutes at 37&deg; C; <br/> 6. Aspirate and wash 5 times; <br/> 7. Add 100&micro; L Substrate Solution. Incubate 10 minutes at 37&deg; C; <br/> 8. Read RLU value immediately.<br/>

Intra-assay Precision (Precision within an assay) : 3 samples with low, middle and high level Enolase 1 (ENO1) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays) : 3 samples with low, middle and high level Enolase 1 (ENO1) were tested on 3 different plates, 8 replicates in each plate. CV (%) = SD/meanX100 Intra-Assay: CV Inter-Assay: CV Inter-Assay: CV

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.

This assay has high sensitivity and excellent specificity for detection of Enolase 1 (ENO1) . No significant cross-reactivity or interference between Enolase 1 (ENO1) and analogues was observed.