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Sunlong Medical™ Human PD-L1/B7-H1/CD274 High Sensitivity ELISA Kit
Sunlong Medical™ Human PD-L1/B7-H1/CD274 High Sensitivity ELISA Kit
CD274 elisa kit | CD274 molecule elisa kit | B7 homolog 1 | B7-H | B7H1 | CD274 antigen | hPD-L1 | MGC142294 | MGC142296 | PD-L1 | PDCD1 ligand 1 | PDCD1L1 | PDCD1LG1 | PDL1 | programmed cell death 1 ligand 1 | programmed death ligand 1
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  • NO.:HS-EL0123Hu
    Species:Human
    Assay range:15.63pg/mL-1000pg/mL
    Sensitivity:0.49 pg/mL
    Sample Volume:20 μL
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:1515
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Details

Cat NO.:
HS-EL0123Hu
Product:
Sunlong Medical™ Human PD-L1/B7-H1/CD274 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% - 115%
Mean Spike Recovery:
1.04
CV of Intra plate:
3.8% - 4.4%
CV of Inter plate:
4.1% - 4.8%
NCBI_Gene:
29126
UniProtKB:
Q9NZQ7

 

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-PD-L1 monoclonal antibody
Human PD-L1 freeze-dried standard
PD-L1 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 PD-L1monoclone 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 PD-L1 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 PD-L1 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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