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Sunlong Medical™ Human GM-CSF ELISA Kit
Sunlong Medical™ Human GM-CSF ELISA Kit
CSF2 elisa kit | colony stimulating factor 2 elisa kit | colony stimulating factor 2 granulocyte-macrophage | colony-stimulating factor | CSF | GMCSF | granulocyte macrophage-colony stimulating factor | granulocyte-macrophage colony stimulating factor |
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  • NO.:EL0061Hu
    Species:Human
    Assay range:1.56pg/mL-100pg/mL
    Sensitivity:4.76 pg/mL
    Sample Volume:20 μL
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:88
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Citations

Cat NO.:
EL0061Hu
Product:
Sunlong Medical™ Human GM-CSF 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:
97% - 110%
Mean Spike Recovery:
1.04
CV of Intra plate:
2.5% - 2.9%
CV of Inter plate:
3.7% - 4.9%
NCBI_Gene:
1437
UniProtKB:
P04141

 

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-GM-CSF monoclonal antibody
Human GM-CSF freeze-dried standard
GM-CSF 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 GM-CSF 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, GM-CSF 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 GM-CSF 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).

 CSF2 upregulates CXCL3 expression in adipocytes to promote metastasis of breast cancer via the FAK signaling pathway

Journal of Molecular Cell Biology 2023-04-18

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