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Sunlong Medical™ Human IL-1β ELISA Kit
Sunlong Medical™ Human IL-1β ELISA Kit
IL1B elisa kit | interleukin 1 beta elisa kit | catabolin | IL-1 | IL-1 beta | IL1-BETA | IL1beta | IL1F2 | interleukin 1 | beta | interleukin 1beta | interleukin-1 beta | preinterleukin 1 beta | pro-interleukin-1-beta
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Regular members: $455.2
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Details

Cat NO.:
EL0285Hu
Product:
Sunlong Medical™ Human 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:
94% - 113%
Mean Spike Recovery:
1.05
CV of Intra plate:
4.7% - 6.1%
CV of Inter plate:
4.1% - 6.6%
NCBI_Gene:
3553
UniProtKB:
P01584

 

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
Human 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-human 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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