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Sunlong Medical™ Human G-CSF ELISA Kit
Sunlong Medical™ Human G-CSF ELISA Kit
CSF3 elisa kit | colony stimulating factor 3 elisa kit | C17orf33 | chromosome 17 open reading frame 33 | colony stimulating factor 3 granulocyte | CSF3OS | filgrastim | G-CSF | GCSF | granulocyte colony-stimulating factor | granulocyte-colony stimulati
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  • NO.:EL0056Hu
    Species:Human
    Assay range:31.25pg/mL-2000pg/mL
    Sensitivity:6.04 pg/mL
    Sample Volume:80 μL 1×Detection buffer and 20 μL Sample
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:112
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Details

Cat NO.:
EL0056Hu
Product:
Sunlong Medical™ Human G-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:
88% - 116%
Mean Spike Recovery:
1.09
CV of Intra plate:
7.4 % - 7.8 %
CV of Inter plate:
8.3 % - 12.6 %
NCBI_Gene:
1440
UniProtKB:
P09919

 

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

 

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