FGF8 ELISA Kit
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- Target See all FGF8 ELISA Kits
- FGF8 (Fibroblast Growth Factor 8 (Androgen-Induced) (FGF8))
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Reactivity
- Human
- Detection Method
- Colorimetric
- Method Type
- Sandwich ELISA
- Detection Range
- 15.6 pg/mL - 1000 pg/mL
- Minimum Detection Limit
- 15.6 pg/mL
- Application
- ELISA
- Sample Type
- Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
- Analytical Method
- Quantitative
- Specificity
- This assay has high sensitivity and excellent specificity for detection of Fibroblast Growth Factor 8, Androgen Induced (FGF8). No significant cross-reactivity or interference between Fibroblast Growth Factor 8, Androgen Induced (FGF8) and analogues was observed.
- Sensitivity
- 6.1 pg/mL
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- Discover our top product FGF8 ELISA Kit
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- Comment
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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 Time
- 3 h
- Plate
- Pre-coated
- Protocol
- The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Fibroblast Growth Factor 8, Androgen Induced (FGF8). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Fibroblast Growth Factor 8, Androgen Induced (FGF8). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Fibroblast Growth Factor 8, Androgen Induced (FGF8), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Fibroblast Growth Factor 8, Androgen Induced (FGF8) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
- Assay Precision
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Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Fibroblast Growth Factor 8, Androgen Induced (FGF8) 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 8, Androgen Induced (FGF8) were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12% - Restrictions
- For Research Use only
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- Handling Advice
- The Stop Solution is acidic. Do not allow to contact skin or eyes. Calibrators, controls and specimen samples should be assayed in duplicate. Once the procedure has been started, all steps should be completed without interruption.
- Storage
- 4 °C,-20 °C
- Storage Comment
- -20°C. Bring all reagents to room temperature before beginning test. The kit may be stored at 4°C for immediate use within two days upon arrival. Reseal any unused strips with desiccant pack. Minimize freeze/thaw cycles.
- Expiry Date
- 4-8 months
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- Target See all FGF8 ELISA Kits
- FGF8 (Fibroblast Growth Factor 8 (Androgen-Induced) (FGF8))
- Alternative Name
- Fibroblast Growth Factor 8, Androgen Induced (FGF8 Products)
- Synonyms
- Aigf ELISA Kit, Fgf-8 ELISA Kit, AIGF ELISA Kit, FGF-8 ELISA Kit, HBGF-8 ELISA Kit, HH6 ELISA Kit, KAL6 ELISA Kit, fibroblast growth factor 8 ELISA Kit, Fgf8 ELISA Kit, FGF8 ELISA Kit
- Background
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Gene Name: Fibroblast Growth Factor 8, Androgen Induced
Gene Aliases: AIGF, HBGF8, Androgen-induced growth factor, Heparin-binding growth factor 8
- Pathways
- RTK Signaling, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Dopaminergic Neurogenesis
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