Human Pro-Collagen Iα1 ELISA KIT

$350.00$450.00

SPECIES Human
Sample Type Serum, plasma, cell culture supernatant, and other biological samples
Sample Volume 100 μL (diluent)
Sensitivity 0.67 pg/mL
Range 15.63 pg/mL – 1000 pg/mL
Assay Time 3.5 h
Recovery 72% – 112%
Average Recovery 0.90
Sample Type Serum, plasma, cell culture supernatant, and other biological samples
Sample Volume 100 μL (diluent)
Sensitivity 0.67 pg/mL
Range 15.63 pg/mL – 1000 pg/mL
Assay Time 3.5 h
Recovery 72% – 112%
Average Recovery 0.90
Intra Precision 2.3% – 3.8%
Inter-Precision 1.0% – 1.2%
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 mouse anti-human Pro-Collagen Iα capture antibody
Human Pro-Collagen Iα1 freeze-dried standard
Human Pro-Collagen Iα1 detect Antibody
Streptavidin-HRP
Assay Buffer(10×)
Substrate TMB
Stop Solution
Washing Buffer(20×)
Sealing Film
Standard Diluent
Assay Principle This kit utilizes the double antibody sandwich enzyme-linked immunosorbent assay (ELISA) detection technique.Specific anti-human Pro-COL I A1 antibodies are precoated on a high-affinity ELISA plate.Standards and test samples are added to the wells of the ELISA plate. After incubation, the Pro-COL I A1 present in the samples binds to the solid-phase antibodies. After washing to remove unbound substances, biotinylated detection antibodies are added and incubated. After washing to remove unbound biotinylated antibodies, 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 Pro-COL I A1 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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