ELK7419-48T, Rat CYP3A5(Cytochrome P450 3A5) ELISA Kit, 48T

ELK7419-48T, Rat CYP3A5(Cytochrome P450 3A5) ELISA Kit, 48T

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ELK7419-96T, Rat CYP3A5(Cytochrome P450 3A5) ELISA Kit, 96T

2.963,10 RON

Rat CYP3A5(Cytochrome P450 3A5) ELISA Kit

SKU
ELK7419-96T

Alternative Names: CP35; P450PCN3; PCN3; Cytochrome P450,Subfamily IIIA(Niphedipine Oxidase),Polypeptide 5; Cytochrome P450 HLp2

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.59 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids

Assay length: 3.5h

Research Area: Tumor immunity;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat CYP3A5. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat CYP3A5. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat CYP3A5, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Rat CYP3A5 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: CP35; P450PCN3; PCN3; Cytochrome P450,Subfamily IIIA(Niphedipine Oxidase),Polypeptide 5; Cytochrome P450 HLp2

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.59 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids

Assay length: 3.5h

Research Area: Tumor immunity;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat CYP3A5. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat CYP3A5. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat CYP3A5, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 Rat CYP3A5 in the samples is then determined by comparing the OD of the samples to the standard curve.