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Sunlong Medical™ Human CXCL1/KC ELISA Kit
Sunlong Medical™ Human CXCL1/KC ELISA Kit
CXCL1 elisa kit | C-X-C motif chemokine ligand 1 elisa kit | C-X-C motif chemokine 1 | chemokine C-X-C motif ligand 1 melanoma growth stimulating activity | alpha | fibroblast secretory protein | FSP | GRO-alpha1-73 | GRO1 | GRO1 oncogene melanoma
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  • NO.:EL0034Hu
    Species:Human
    Assay range:0.78pg/mL-50pg/mL
    Sensitivity:0.10 pg/mL
    Sample Volume:100 μL(diluent)
    Assay type:Sandwich Method
    Validity:Two Years
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Citations

Cat NO.:
EL0034Hu
Product:
Sunlong Medical™ Human CXCL1/KC 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:
73% - 102%
Mean Spike Recovery:
0.92
CV of Intra plate:
2.8% - 11.0%
CV of Inter plate:
4.7% - 8.4%
NCBI_Gene:
2919
UniProtKB:
P09341

 

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-CXCL1/CK monoclonal antibody
Human CXCL1/CK freeze-dried standard
Angiotensinogen/AGT/ SerpinA8 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 CXCL1 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 CXCL1 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, 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 CXCL1 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).

 

 1. The spike protein of SARS-CoV-2 induces inflammation and EMT of lung epithelial cells and fibroblasts through the upregulation of GADD45A

Open Medicine 2023-11-15
 
Cancer Discovery 2023-07-24
 
Journal of Molecular Cell Biology 2023-04-18

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