ELISA Kit for Fibroblast Growth Factor 13 (FGF13)

Enzyme-linked immunosorbent assay for Antigen Detection.

Product No.

CEC915Hu

Organism Species

Homo sapiens (Human).

Sample Type

serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Test Method

Competitive Inhibition

Assay Length

2h

Detection Range

31.2-500pg/mL

Sensitivity

The minimum detectable dose of this kit is typically less than 13.1pg/mL.

UOM

48T 96T 96T*5 96T*10 96T*100

Specificity

This assay has high sensitivity and excellent specificity for detection of Fibroblast Growth Factor 13 (FGF13).
No significant cross-reactivity or interference between Fibroblast Growth Factor 13 (FGF13) and analogues was observed.

Recovery

Matrices listed below were spiked with certain level of recombinant Fibroblast Growth Factor 13 (FGF13) and the recovery rates were calculated by comparing the measured value to the expected amount of Fibroblast Growth Factor 13 (FGF13) in samples.

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Fibroblast Growth Factor 13 (FGF13) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Fibroblast Growth Factor 13 (FGF13) were tested on 3 different plates, 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 Fibroblast Growth Factor 13 (FGF13) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Stability

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.

Reagents and materials provided

Assay procedure summary

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 3 times;
   4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
   5. Aspirate and wash 5 times;
   6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
   7. Add 50µL Stop Solution. Read at 450 nm immediately.