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Sunlong Medical™ Human RAGE ELISA Kit
Sunlong Medical™ Human RAGE ELISA Kit
MOK elisa kit | MOK protein kinase elisa kit | MAPK/MAK/MRK overlapping kinase | RAGE | RAGE-1 | RAGE1 | renal cell carcinoma antigen | renal cell carcinoma antigen MOK protein kinase | renal tumor antigen 1 | STK30
Total
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Regular members: $455.2

Details

Cat NO.:
EL0267Hu
Product:
Sunlong Medical™ Human RAGE 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:
89% - 108%
Mean Spike Recovery:
1
CV of Intra plate:
3.4 % - 5.0 %
CV of Inter plate:
5.2 % - 5.9 %
NCBI_Gene:
5891
UniProtKB:
Q9UQ07

 

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 anti-RAGE monoclonal antibody
Human RAGE freeze-dried standard
RAGE detect Antibody
Standard Diluent
Assay Buffer(10×)
Substrate TMB
Stop Solution
Washing Buffer(20×)
Sealing Film
ASSAY PRINCIPLE This kit utilizes the double antibody sandwich enzyme-linked immunosorbent assay (ELISA) detection technique.Specific anti-human RAGE antibodies are precoated on a high-affinity ELISA plate. Standard samples, test samples, and biotinylated detection antibodies are added to the wells of the ELISA plate. After incubation, RAGE present in the samples binds to the solid-phase antibodies and the detection antibodies. After washing to remove unbound substances, streptavidin-HRP labeled with horseradish peroxidase is added. 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 RAGE 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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