ELK6215-96T, Human WNT10B(Wingless Type MMTV Integration Site Family, Member 10B) ELISA Kit, 96T

ELK6215-96T, Human WNT10B(Wingless Type MMTV Integration Site Family, Member 10B) ELISA Kit, 96T

ELK6216-96T, Rat NRF1(Nuclear Respiratory Factor 1) ELISA Kit, 96T

ELK6216-96T, Rat NRF1(Nuclear Respiratory Factor 1) ELISA Kit, 96T

ELK6216-48T, Rat NRF1(Nuclear Respiratory Factor 1) ELISA Kit, 48T

2.142,00 RON

Rat NRF1(Nuclear Respiratory Factor 1) ELISA Kit

SKU
ELK6216-48T

Alternative Names: ALPHA-PAL; EWG; Alpha Palindromic-Binding Protein

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.055 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 Rat NRF1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NRF1. 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 NRF1, 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 NRF1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ALPHA-PAL; EWG; Alpha Palindromic-Binding Protein

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.055 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 Rat NRF1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NRF1. 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 NRF1, 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 NRF1 in the samples is then determined by comparing the OD of the samples to the standard curve.