ELK9273-48T, Rat ST2( Suppression Of Tumorigenicity 2) ELISA Kit, 48T

ELK9273-48T, Rat ST2( Suppression Of Tumorigenicity 2) ELISA Kit, 48T

ELK9274-48T, Rat CTN(Creatinine) ELISA Kit, 48T

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ELK9273-96T, Rat ST2( Suppression Of Tumorigenicity 2) ELISA Kit, 96T

2.963,10 RON

Rat ST2( Suppression Of Tumorigenicity 2) ELISA Kit

SKU
ELK9273-96T

Alternative Names: ST2;IL1RL1

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.065 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

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

Assay length: 3.5h

Research Area: CD & Adhesion molecule

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 ST2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ST2. 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 ST2, 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 ST2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ST2;IL1RL1

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.065 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

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

Assay length: 3.5h

Research Area: CD & Adhesion molecule

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 ST2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ST2. 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 ST2, 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 ST2 in the samples is then determined by comparing the OD of the samples to the standard curve.