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Sunlong Medical™ Human Apolipoprotein D/Apo D ELISA Kit
Sunlong Medical™ Human Apolipoprotein D/Apo D ELISA Kit
APOD elisa kit | apolipoprotein D elisa kit | apo-D
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  • NO.:EL0149Hu
    Species:Human
    Assay range:0.63ng/mL-40ng/mL
    Sensitivity:25.67 pg/mL
    Sample Volume:90 μL 1×Detection buffer and 10 μL Pre-diluted sample
    Assay type:Sandwich Method
    Validity:Two Years
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Details

Cat NO.:
EL0149Hu
Product:
Sunlong Medical™ Human Apolipoprotein D/Apo D 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:
85% - 103%
Mean Spike Recovery:
0.91
CV of Intra plate:
2.0% - 8.1%
CV of Inter plate:
1.9%-2.8%
NCBI_Gene:
347
UniProtKB:
P05090

 

SAMPLE VOLUME 90 μL 1×Assay Buffer and 10 μL prediluted sample
SENSITIVITY 25.67 pg/mL
RANGE 0.63 ng/mL – 40 ng/mL
ASSAY TIME 3.5 h
RECOVERY 85% – 103%
AVERAGE RECOVERY 0.91
INTRA PRECISION 2.0% – 8.1%
INTER-PRECISION 1.9%-2.8%
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-Apolipoprotein D/Apo D monoclonal antibody
Human Apolipoprotein D/Apo D freeze-dried standard
Apolipoprotein D/Apo D 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 Apo D 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, Apo D 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 Apo D 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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