ELK9190-48T, Rat EDA(Ectodysplasin-A) ELISA Kit, 48T

ELK9190-48T, Rat EDA(Ectodysplasin-A) ELISA Kit, 48T

ELK9191-48T, Dog MBP(Myelin Basic Protein) ELISA Kit, 48T

ELK9191-48T, Dog MBP(Myelin Basic Protein) ELISA Kit, 48T

ELK9190-96T, Rat EDA(Ectodysplasin-A) ELISA Kit, 96T

2.963,10 RON

Rat EDA(Ectodysplasin-A) ELISA Kit

SKU
ELK9190-96T

Alternative Names: Eda; Ed1; TaEctodysplasin-A; EDA protein homolog; Tabby protein Cleaved into: Ectodysplasin-A; Ectodysplasin-A;

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.058 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Developmental Biology

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

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Description

Alternative Names: Eda; Ed1; TaEctodysplasin-A; EDA protein homolog; Tabby protein Cleaved into: Ectodysplasin-A; Ectodysplasin-A;

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.058 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Developmental Biology

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