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Sunlong Medical™ Rat CXCL2/CINC-3 ELISA Kit
Sunlong Medical™ Rat CXCL2/CINC-3 ELISA Kit
CXCL2 elisa kit | C-X-C motif chemokine ligand 2 elisa kit | C-X-C motif chemokine 2 | chemokine C-X-C motif ligand 2 | CINC-3 | cytokine-induced neutrophil chemoattractant 3 | macrophage inflammatory protein 2 | Mip-2 | MIP2 | Scyb2 | small inducible c
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Regular members: $455.2
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  • NO.:EL0027Ra
    Species:Rat
    Assay range:31.25pg/mL-2000pg/mL
    Sensitivity:1.84 pg/mL
    Sample Volume:80 μL 1×Detection buffer and 20 μL Sample
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:143
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Details

Cat NO.:
EL0027Ra
Product:
Sunlong Medical™ Rat CXCL2/CINC-3 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:
76% - 133%
Mean Spike Recovery:
1.01
CV of Intra plate:
3.2 % - 5.8 %
CV of Inter plate:
3.8 % - 5.5 %
NCBI_Gene:
114105
UniProtKB:
P30348

 

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-CXCL2/CINC-3 monoclonal antibody
Rat CXCL2/CINC-3 freeze-dried standard
CXCL2/CINC-3 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-rat CXCL2 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, CXCL2 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 CXCL2 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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