ELK8379-48T, Mouse 8-iso-PGF2α(8-isoprostane) ELISA Kit, 48T

ELK8379-48T, Mouse 8-iso-PGF2α(8-isoprostane) ELISA Kit, 48T

ELK8380-48T, Mouse PARP2(Poly [ADP-ribose] polymerase 2) ELISA Kit, 48T

ELK8380-48T, Mouse PARP2(Poly [ADP-ribose] polymerase 2) ELISA Kit, 48T

ELK8379-96T, Mouse 8-iso-PGF2α(8-isoprostane) ELISA Kit, 96T

2.963,10 RON

Mouse 8-iso-PGF2α(8-isoprostane) ELISA Kit

SKU
ELK8379-96T

Alternative Names: 8-isoprostane; 8-iso-PGF2α

Species: Mouse

Assay Type: Competitive Inhibition

Sensitivity: 9.375 pg/mL

Standard: 1000 pg/mL

Detection range: 15.625-1000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Endocrinology;Pulmonology;Hepatology;Hormone metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse 8-iso-PGF2α protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse 8-iso-PGF2α. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse 8-iso-PGF2α in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: 8-isoprostane; 8-iso-PGF2α

Species: Mouse

Assay Type: Competitive Inhibition

Sensitivity: 9.375 pg/mL

Standard: 1000 pg/mL

Detection range: 15.625-1000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Endocrinology;Pulmonology;Hepatology;Hormone metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse 8-iso-PGF2α protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse 8-iso-PGF2α. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse 8-iso-PGF2α in the samples is then determined by comparing the OD of the samples to the standard curve.