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Sunlong Medical™ Human/Mouse/Rat TGF-β2 ELISA Kit
Sunlong Medical™ Human/Mouse/Rat TGF-β2 ELISA Kit
TGFB2 elisa kit | transforming growth factor beta 2 elisa kit | BSC-1 cell growth inhibitor | cetermin | G-TSF | glioblastoma-derived T-cell suppressor factor | LDS4 | MGC116892 | polyergin | prepro-transforming growth factor beta-2 | TGF-beta-2 | TGF-bet
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  • NO.:EL0015Hu
    Species:Human
    Assay range:31.25pg/mL-2000pg/mL
    Sensitivity:0.33 pg/mL
    Sample Volume:100 μL
    Assay type:Sandwich Method
    Validity:Two Years
  • Goods click count:92
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Cat NO.:
EL0015Hu
Product:
Sunlong Medical™ Human/Mouse/Rat TGF-β2 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:
88% - 120%
Mean Spike Recovery:
1.07
CV of Intra plate:
2.7 % - 4.5 %
CV of Inter plate:
3.3 % - 4.8%
NCBI_Gene:
7042
UniProtKB:
P61812

 

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-TGF-β2 monoclonal antibody
Human /Mouse /Rat TGF-β2 freeze-dried standard
TGF-β2 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 /mouse /rat TGF-β2 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, TGF-β2 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 TGF-β2 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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