ELISA Kit for Fibroblast Growth Factor 23 (FGF23)
Size: 96T
Catalogue Number: UCEA746Ra-96
Citations, Manuals and MSDS Available upon request.
Target: Fibroblast Growth Factor 23 (FGF23)
Alternative Names: ADHR; HYPF; HPDR2; PHPTC; Phosphatonin; Tumor-derived hypophosphatemia-inducing factor
Target Species: Rat
Detection range: 62.5-1,000pg/mL
Sensitivity: 21.6pg/mL
Uniprot: Q8VI82
Gene ID: 170583
Featured Series Function: Detects small molecule
Recommended/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids
Assay Time: 2h
Method: Colormetric
Specificity: Reactive with Rat FGF23 / Fibroblast Growth Factor 23
Detection principle: Competitive Inhibition
Sample Size: 50uL
Assay Precision: Intra-Assay: CV<10%, Inter-Assay: CV<12%
Storage: 4°C for 1 month/ -20°C for long-term(One year within shelf life)
Shelf-life: 12 months
Specificity: This assay has high sensitivity and excellent specificity for detection of Fibroblast Growth Factor 23 (FGF23).
No significant cross-reactivity or interference between Fibroblast Growth Factor 23 (FGF23) and analogues was observed.
Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Fibroblast Growth Factor 23 (FGF23) 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 23 (FGF23) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
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.
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.
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Fibroblast Growth Factor 23 (FGF23) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Fibroblast Growth Factor 23 (FGF23) and unlabeled Fibroblast Growth Factor 23 (FGF23) (Standards or samples) with the pre-coated antibody specific to Fibroblast Growth Factor 23 (FGF23). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Fibroblast Growth Factor 23 (FGF23) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Fibroblast Growth Factor 23 (FGF23) in the sample.
Research Area: Cytokine; Tumor immunity; Infection immunity; Genetic science;
Research Use Only