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Sunlong Medical™ Human CXCL11/I-TAC ELISA Kit
Sunlong Medical™ Human CXCL11/I-TAC ELISA Kit
CXCL11 elisa kit | C-X-C motif chemokine ligand 11 elisa kit | b-R1 | beta-R1 | C-X-C motif chemokine 11 | chemokine C-X-C motif ligand 11 | H174 | I-TAC | interferon gamma-inducible protein 9 | interferon-inducible T-cell alpha chemoattractant | IP-9 |
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  • NO.:EL0165Hu
    Species:Human
    Assay range:3.91pg/mL-250pg/mL
    Sensitivity:0.78 pg/mL
    Sample Volume:10 μL
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:121
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Details

Cat NO.:
EL0165Hu
Product:
Sunlong Medical™ Human CXCL11/I-TAC 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:
84% - 110%
Mean Spike Recovery:
0.94
CV of Intra plate:
2.5 % - 4.8 %
CV of Inter plate:
4.4 % - 5.0 %
NCBI_Gene:
6373
UniProtKB:
O14625

 

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-CXCL11/I-TAC monoclonal antibody
Human CXCL11/I-TAC freeze-dried standard
CXCL11/I-TAC 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 CXCL11 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, CXCL11 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 CXCL11 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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