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Sunlong Medical™ Human CXCL-10/IP-10 ELISA Kit
Sunlong Medical™ Human CXCL-10/IP-10 ELISA Kit
CXCL10 elisa kit | C-X-C motif chemokine ligand 10 elisa kit | 10 kDa interferon gamma-induced protein | C-X-C motif chemokine 10 | C7 | chemokine C-X-C motif ligand 10 | crg-2 | gamma IP10 | gamma-IP10 | gIP-10 | IFI10 | INP10 | interferon-inducible cy
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  • NO.:EL0057Hu
    Species:Human
    Assay range:31.25pg/mL-2000pg/mL
    Sensitivity:3.50 pg/mL
    Sample Volume:50 μL
    Assay type:Sandwich Method
    Validity:Two Years
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Cat NO.:
EL0057Hu
Product:
Sunlong Medical™ Human CXCL-10/IP-10 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:
78% - 114%
Mean Spike Recovery:
0.93
CV of Intra plate:
3.0 % - 5.0 %
CV of Inter plate:
3.8 % - 6.1 %
NCBI_Gene:
3627
UniProtKB:
P02778

 

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-CXCL10/IP-10 monoclonal antibody
Human CXCL10/IP-10 freeze-dried standard
CXCL10/IP-10 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 IP-10 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, IP-10 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 IP-10 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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