ELK8024-48T, Rat PER2(Period Circadian Protein 2) ELISA Kit, 48T

ELK8024-48T, Rat PER2(Period Circadian Protein 2) ELISA Kit, 48T

ELK8025-48T, Rat gSAP(Gamma-Secretase Activating Protein) ELISA Kit, 48T

ELK8025-48T, Rat gSAP(Gamma-Secretase Activating Protein) ELISA Kit, 48T

ELK8024-96T, Rat PER2(Period Circadian Protein 2) ELISA Kit, 96T

2.963,10 RON

Rat PER2(Period Circadian Protein 2) ELISA Kit

SKU
ELK8024-96T

Alternative Names: FASPS; Circadian clock protein PERIOD 2

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.101 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Neuro science;

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 PER2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat PER2. 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 PER2, 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 PER2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: FASPS; Circadian clock protein PERIOD 2

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.101 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Neuro science;

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 PER2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat PER2. 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 PER2, 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 PER2 in the samples is then determined by comparing the OD of the samples to the standard curve.