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Sunlong Medical™ Mouse CD30/TNFRSF8 ELISA Kit
Sunlong Medical™ Mouse CD30/TNFRSF8 ELISA Kit
TNFRSF8 elisa kit | TNF receptor superfamily member 8 elisa kit | CD30 | Cd30 | CD30 antigen
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  • NO.:EL0049Mo
    Species:Mouse
    Assay range:15.63pg/mL-1000pg/mL
    Sensitivity:0.88 pg/mL
    Sample Volume:100 μL(diluent)
    Assay type:Sandwich Method
    Validity:Two Years
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Details

Cat NO.:
EL0049Mo
Product:
Sunlong Medical™ Mouse CD30/TNFRSF8 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:
92% - 118%
Mean Spike Recovery:
1.06
CV of Intra plate:
3.5 % - 4.7 %
CV of Inter plate:
1.1 % - 2.8 %
NCBI_Gene:
21941
UniProtKB:
Q60846

 

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-CD30 monoclonal antibody
Human CD30 freeze-dried standard
Angiotensinogen/AGT/ SerpinA8 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 BMP-4 antibodies are precoated on a high-affinity ELISA plate. Standard samples, test samples, and the detection antibody labeled with horseradish peroxidase are added to the wells of the ELISA plate. After incubation, CD30 present in the samples binds to the solid-phase antibodies and the detection antibodies. 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 CD30 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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