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Sunlong Medical™ Human FGFR2 ELISA Kit
Sunlong Medical™ Human FGFR2 ELISA Kit
FGFR2 elisa kit | fibroblast growth factor receptor 2 elisa kit | bacteria-expressed kinase | BBDS | BEK | BEK fibroblast growth factor receptor | BFR-1 | CD332 | CEK3 | CFD1 | ECT1 | FGF receptor | FGFR-2 | FGFR2-AHCYL1 fusion kinase protein | fibroblast
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Details

Cat NO.:
EL0001Hu
Product:
Sunlong Medical™ Human FGFR2 ELISA Kit
Storage
4℃ (unopened) for two years
Shipping Condition
4℃
Sample Type:
Serum | plasma | cell culture supernatant and other biological samples
Spike Recovery Range:
87% - 119%
Mean Spike Recovery:
1.07
CV of Intra plate:
3.0 % - 7.6 %
CV of Inter plate:
5.1 % - 6.8 %
NCBI_Gene:
2263
UniProtKB:
P21802

 

PLATFORM ELISA
PLATE Detachable 96-well plate
SIZE 96T/48T
STORAGE If the reagent kit is unopened, it should be stored at 4℃. However, if it has been opened, the standard solution should be stored at -20℃, while the other components should be stored at 4℃.
DELIVERY 4℃ blue ice transportation
COMPONENTS 96-well polystyrene enzyme-linked immunosorbent assay (ELISA) plate coated with mouse anti-human FGFR2 capture antibody
Human FGFR2 freeze-dried standard
Streptavidin-HRP标记Human FGFR2单克隆 detect Antibody
Assay Buffer(10×)
Substrate TMB
Stop Solution
Washing Buffer(20×)
Sealing Film
Standard Diluent
ASSAY PRINCIPLE

This kit utilizes the double antibody sandwich enzyme-linked immunosorbent assay (ELISA) detection technique.Specific anti-human FGFR2 antibodies are precoated on a high-affinity ELISA plate.Standards and test samples are added to the wells of the ELISA plate. After incubation, the FGFR2 present in the samples binds to the solid-phase antibodies. After washing to remove unbound substances, detection antibodies labeled with horseradish peroxidase (HRP) are added and incubated. After washing, a colorimetric substrate, TMB, is added and the plate is incubated in the dark for color development. The intensity of the color reaction is directly proportional to the concentration of FGFR2 in the samples.A stop solution is added to terminate the reaction, and the absorbance value is measured at a wavelength of 450 nm (with a reference wavelength range of 570-630 nm).

 

 

 

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