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Sunlong Medical™ Human sIL-2Ra/CD25 ELISA Kit
Sunlong Medical™ Human sIL-2Ra/CD25 ELISA Kit
IL2RA elisa kit | interleukin 2 receptor subunit alpha elisa kit | CD25 | IDDM10 | IL-2 receptor subunit alpha | IL-2-RA | IL-2R subunit alpha | IL2-RA | IL2R | IMD41 | insulin-dependent diabetes mellitus 10 | interleukin 2 receptor | alpha | interleukin
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  • NO.:EL0039Hu
    Species:Human
    Assay range:78.13pg/mL-5000pg/mL
    Sensitivity:2.99 pg/mL
    Sample Volume:80 μL 1×Detection buffer and 20 μL Sample
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:105
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Details

Cat NO.:
EL0039Hu
Product:
Sunlong Medical™ Human sIL-2Ra/CD25 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% - 104%
Mean Spike Recovery:
1.02
CV of Intra plate:
4.8 % - 7.5 %
CV of Inter plate:
4.4 % - 7.9 %
NCBI_Gene:
3559
UniProtKB:
P01589

 

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-sIL-2Rα/CD25 monoclonal antibody
Human sIL-2Rα/CD25 freeze-dried standard
sIL-2Rα/CD25 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 sIL-2Rα 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, sIL-2Rα 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 sIL-2Rα 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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