ELK7021-48T, Rat NUCB1(Nucleobindin 1) ELISA Kit, 48T

ELK7021-48T, Rat NUCB1(Nucleobindin 1) ELISA Kit, 48T

ELK7022-48T, Rat NUCB2(Nucleobindin 2) ELISA Kit, 48T

ELK7022-48T, Rat NUCB2(Nucleobindin 2) ELISA Kit, 48T

ELK7021-96T, Rat NUCB1(Nucleobindin 1) ELISA Kit, 96T

2.963,10 RON

Rat NUCB1(Nucleobindin 1) ELISA Kit

SKU
ELK7021-96T

Alternative Names: NUC; CALNUC

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.063 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: 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 Rat NUCB1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NUCB1. 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 NUCB1, 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 NUCB1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: NUC; CALNUC

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.063 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: 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 Rat NUCB1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NUCB1. 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 NUCB1, 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 NUCB1 in the samples is then determined by comparing the OD of the samples to the standard curve.