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Sunlong Medical™ Human CXCL12/SDF-1 ELISA Kit
Sunlong Medical™ Human CXCL12/SDF-1 ELISA Kit
CXCL12 elisa kit | C-X-C motif chemokine ligand 12 elisa kit | chemokine C-X-C motif ligand 12 | intercrine reduced in hepatomas | IRH | PBSF | pre-B cell growth-stimulating factor | SCYB12 | SDF-1a | SDF-1b | SDF1 | SDF1A | SDF1B | stromal cell-derived
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  • NO.:EL0249Hu
    Species:Human
    Assay range:62.5pg/mL-4000pg/mL
    Sensitivity:18.13 pg/mL
    Sample Volume:20 μL
    Assay type:Sandwich Method
    Validity:Two Years
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Citations

Cat NO.:
EL0249Hu
Product:
Sunlong Medical™ Human CXCL12/SDF-1 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:
89% - 110%
Mean Spike Recovery:
1.02
CV of Intra plate:
2.4 % - 2.6 %
CV of Inter plate:
3.0 % - 4.5 %
NCBI_Gene:
6387
UniProtKB:
P48061

 

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-CXCL12/SDF-1 monoclonal antibody
Human CXCL12/SDF-1 freeze-dried standard
CXCL12/SDF-1 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 CXCL12 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, CXCL12 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 CXCL12 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).

 

1. Cascade Regulation of the Proliferation, Recruitment, and Differentiation of Stem Cells to Prevent Aseptic Loosening by GNPs/ECPP Particles Responding to Macrophages: In Vitro and In Vivo

ACS Biomaterials Science & Engineering 2023-03-31
 
PHYTOMEDICINE 2023-06-16
 
CANCER LETTERS 2023-06-09

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