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Sunlong Medical™ Human G-CSF High Sensitivity ELISA Kit
Sunlong Medical™ Human G-CSF High Sensitivity 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.:HS-EL0055Hu
    Species:Human
    Assay range:15.63pg/mL-1000pg/mL
    Sensitivity:0.19 pg/mL
    Sample Volume:Serum | plasma;50 μL;Cell culture supernatant;100 μL
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:139
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Details

Cat NO.:
HS-EL0055Hu
Product:
Sunlong Medical™ Human G-CSF 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:
94% - 119%
Mean Spike Recovery:
1.06
CV of Intra plate:
4.1% - 4.8%
CV of Inter plate:
4.4% - 4.9%
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 high sensitivity freeze-dried standard
G-CSF 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 G-CSF 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 G-CSF 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 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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