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Sunlong Medical™ Rat IL-17A High Sensitivity ELISA Kit
Sunlong Medical™ Rat IL-17A High Sensitivity ELISA Kit
IL17A elisa kit | interleukin 17A elisa kit | CTLA-8 | cytotoxic T-lymphocyte-associated antigen 8 | hypothetical protein LOC301289 | IL-17 | IL-17A | Il17 | interleukin 17 | Interleukin 17 cytotoxic T-lymphocyte-associated serine esterase 8 | interleuk
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  • NO.:HS-EL0025Ra
    Species:Rat
    Assay range:1.56pg/mL-100pg/mL
    Sensitivity:0.15 pg/mL
    Sample Volume:20 μL
    Assay type:Sandwich Method
    Validity:Two Years
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Details

Cat NO.:
HS-EL0025Ra
Product:
Sunlong Medical™ Rat IL-17A 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:
94% - 117%
Mean Spike Recovery:
1.02
CV of Intra plate:
2.5% - 4.5%
CV of Inter plate:
2.9% - 4.5%
NCBI_Gene:
301289
UniProtKB:
G3V7M4
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-17AA monoclonal antibody
Rat IL-17AA freeze-dried standard
IL-17AA 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-17A 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-17A 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-17A 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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