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Sunlong Medical™ Rat IFN-γ  High Sensitivity ELISA Kit
Sunlong Medical™ Rat IFN-γ High Sensitivity ELISA Kit
IFNG elisa kit | interferon gamma elisa kit | If2f | IFN-gamma | IFNG2 | interferon 2f
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  • NO.:HS-EL0014Ra
    Validity:Two Years
    Assay type:Sandwich Method
    Sample Volume:20 μL
    Sensitivity:0.26 pg/mL
    Assay range:3.13 pg/mL – 200 pg/mL
    Species:Rat
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Details

Cat NO.:
HS-EL0014Ra
Product:
Sunlong Medical™ Rat IFN-γ ELISA KitHS
Storage
4℃ (unopened) for two years
Shipping Condition
4℃
Sample Type:
Serum | plasma | cell culture supernatant and other biological samplesHS
Spike Recovery Range:
73% – 137%
Mean Spike Recovery:
S0.93
CV of Intra plate:
3.7% – 4.4%
CV of Inter plate:
2.4% – 8.5%
NCBI_Gene:
P01581
UniProtKB:
A0A7R8C3J6

 

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-IFN-γA monoclonal antibody
Rat IFN-γA freeze-dried standard
IFN-γA 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 IFN-γ 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 IFN-γ 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 IFN-γ 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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