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Sunlong Medical™ Human CXCL5/ENA-78 ELISA Kit
Sunlong Medical™ Human CXCL5/ENA-78 ELISA Kit
CXCL5 elisa kit | C-X-C motif chemokine ligand 5 elisa kit | C-X-C motif chemokine 5 | chemokine C-X-C motif ligand 5 | ENA-78 | ENA-781-78 | epithelial-derived neutrophil activating protein 78 | epithelial-derived neutrophil-activating peptide 78 | e
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  • NO.:EL0153Hu
    Species:Human
    Assay range:31.25pg/mL-2000pg/mL
    Sensitivity:13.45 pg/mL
    Sample Volume:10 μL
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:77
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Cat NO.:
EL0153Hu
Product:
Sunlong Medical™ Human CXCL5/ENA-78 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% - 125%
Mean Spike Recovery:
1.01
CV of Intra plate:
4.9 % - 6.4 %
CV of Inter plate:
2.8 % - 3.9 %
NCBI_Gene:
6374
UniProtKB:
P42830

 

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-CXCL5 monoclonal antibody
Human CXCL5 freeze-dried standard
CXCL5 detect Antibody
Standard Diluent
HRP-labeled streptavidin
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 CXCL5 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 CXCL5 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, the TMB chromogenic substrate is added, and color development is carried out while avoiding light. The intensity of the color reaction is directly proportional to the concentration of CXCL5 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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