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Sunlong Medical™ Rat IL-1β ELISA Kit
Sunlong Medical™ Rat IL-1β ELISA Kit
IL1B elisa kit | interleukin 1 beta elisa kit | IL-1 beta | IL-1F2 | interleukin-1 beta
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  • NO.:EL0040Ra
    Species:Rat
    Assay range:31.25pg/mL-2000pg/mL
    Sensitivity:1.42 pg/mL
    Sample Volume:20 μL
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:114
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Cat NO.:
EL0040Ra
Product:
Sunlong Medical™ Rat IL-1β 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:
84% - 110%
Mean Spike Recovery:
1.02
CV of Intra plate:
5.0 % - 5.1 %
CV of Inter plate:
5.5 % - 6.7 %
NCBI_Gene:
24494
UniProtKB:
Q5BKB0

 

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-IL-1β monoclonal antibody
Rat IL-1β freeze-dried standard
IL-1β 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-rat IL-1β 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, IL-1β 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 IL-1β 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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