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Sunlong Medical™ Human B7-1/CD80 ELISA Kit
Sunlong Medical™ Human B7-1/CD80 ELISA Kit
CD80 elisa kit | CD80 molecule elisa kit | activation B7-1 antigen | B-lymphocyte activation antigen B7 | B7 | B7-1 | B7.1 | BB1 | CD28LG | CD28LG1 | cd80 antigen | CD80 antigen CD28 antigen ligand 1 | B7-1 antigen | costimulatory factor CD80 | costimul
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  • NO.:EL0112Hu
    Species:Human
    Assay range:7.81pg/mL-500pg/mL
    Sensitivity:0.72 pg/mL
    Sample Volume:50 μL 1×Detection buffer and 50 μL Sample
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:116
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Details

Cat NO.:
EL0112Hu
Product:
Sunlong Medical™ Human B7-1/CD80 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:
82% - 102%
Mean Spike Recovery:
0.91
CV of Intra plate:
3.7% - 5.0%
CV of Inter plate:
2.8%-6.6%
NCBI_Gene:
941
UniProtKB:
P33681

 

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-B7-1/CD80 monoclonal antibody
Human B7-1/CD80 freeze-dried standard
B7-1/CD80 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 CD80 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, CD80 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 CD80 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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