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Sunlong Medical™ Mouse CXCL1/KC ELISA Kit
Sunlong Medical™ Mouse CXCL1/KC ELISA Kit
CXCL1 elisa kit | C-X-C motif chemokine ligand 1 elisa kit | fibroblast secretory protein | Fsp | Gro1 | GRO1 oncogene | KC | KC/GRO-alpha | melanoma growth stimulatory activity | Mgsa | N51 | Scyb1
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  • NO.:EL0012Mo
    Species:Mouse
    Assay range:31.25pg/mL-2000pg/mL
    Sensitivity:0.47 pg/mL
    Sample Volume:20 μL
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:82
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Details

Citations

Cat NO.:
EL0012Mo
Product:
Sunlong Medical™ Mouse 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:
91% - 107%
Mean Spike Recovery:
0.98
CV of Intra plate:
3.9 % - 5.6 %
CV of Inter plate:
4.4 % - 5.9 %
NCBI_Gene:
14825
UniProtKB:
P12850

 

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/KC monoclonal antibody
Mouse CXCL1/KC freeze-dried standard
CXCL1/KC 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-mouse CXCL1 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, CXCL1 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 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).

 











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