ELK0673-48T, Human ERG(Transcriptional regulator ERG) ELISA Kit, 48T

ELK0673-48T, Human ERG(Transcriptional regulator ERG) ELISA Kit, 48T

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ELK0673-96T, Human ERG(Transcriptional regulator ERG) ELISA Kit, 96T

2.963,10 RON

Human ERG(Transcriptional regulator ERG) ELISA Kit

SKU
ELK0673-96T

Alternative Names: Transcriptional regulator ERG

Species: Human

Assay Type: Sandwich

Sensitivity: 0.061 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: serum, plasma, tissue homogenates, saliva, cell lysates, follicular fluid and other biological fluids

Assay length: 3.5h

Research Area: Signal transduction;

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

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Description

Alternative Names: Transcriptional regulator ERG

Species: Human

Assay Type: Sandwich

Sensitivity: 0.061 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: serum, plasma, tissue homogenates, saliva, cell lysates, follicular fluid and other biological fluids

Assay length: 3.5h

Research Area: Signal transduction;

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