ELK4688-96T, Human CYP27A1(Cytochrome P450 27A1) ELISA Kit, 96T

ELK4688-96T, Human CYP27A1(Cytochrome P450 27A1) ELISA Kit, 96T

ELK4689-96T, Human LMNB2(Lamin B2) ELISA Kit, 96T

ELK4689-96T, Human LMNB2(Lamin B2) ELISA Kit, 96T

ELK4689-48T, Human LMNB2(Lamin B2) ELISA Kit, 48T

2.142,00 RON

Human LMNB2(Lamin B2) ELISA Kit

SKU
ELK4689-48T

Alternative Names: LMN2; LAMB2

Species: Human

Assay Type: Sandwich

Sensitivity: 0.051 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

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

Assay length: 3.5h

Research Area: Metabolic pathway;

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 Human LMNB2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LMNB2. 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 Human LMNB2, 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 Human LMNB2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: LMN2; LAMB2

Species: Human

Assay Type: Sandwich

Sensitivity: 0.051 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

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

Assay length: 3.5h

Research Area: Metabolic pathway;

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 Human LMNB2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LMNB2. 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 Human LMNB2, 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 Human LMNB2 in the samples is then determined by comparing the OD of the samples to the standard curve.