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Sunlong Medical™ Human IL-22 High Sensitivity ELISA Kit
Sunlong Medical™ Human IL-22 High Sensitivity ELISA Kit
IL22 elisa kit | interleukin 22 elisa kit | cytokine Zcyto18 | IL-10-related T-cell-derived inducible factor | IL-10-related T-cell-derived-inducible factor | IL-21 | IL-22 | IL-D110 | IL-TIF | IL21 | ILTIF | interleukin 21 | interleukin-22 | MGC79382 | M
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  • NO.:HS-EL0145Hu
    Species:Human
    Assay range:6.25pg/mL-400pg/mL
    Sensitivity:0.67 pg/mL
    Sample Volume:Serum | plasma;20 μL;Cell culture supernatant;100 μL
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:132
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Details

Cat NO.:
HS-EL0145Hu
Product:
Sunlong Medical™ Human IL-22 High Sensitivity 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:
92% - 117%
Mean Spike Recovery:
1.05
CV of Intra plate:
4.1% - 4.8%
CV of Inter plate:
3.8% - 4.7%
NCBI_Gene:
50616
UniProtKB:
Q9GZX6

 

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-22 monoclonal antibody
Human IL-22 high sensitivity freeze-dried standard
IL-22 detect Antibody
Standard Diluent
HRP-labeled streptavidin
Signal enhancer concentrate
Signal enhancer 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-22 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 IL-22 present in the samples binds to the solid-phase antibodies. After washing to remove unbound substances, biotinylated detection antibodies are added and incubated. After washing to remove unbound biotinylated antibodies, streptavidin-HRP labeled with horseradish peroxidase is added. After washing again, a signal enhancer is added and incubated. After washing to remove unbound substances, Streptavidin-HRP is added once more. 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-22 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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