ELK2607-96T, Rat TRH(Thyrotropin Releasing Hormone) ELISA Kit, 96T

ELK2607-96T, Rat TRH(Thyrotropin Releasing Hormone) ELISA Kit, 96T

ELK2608-96T, Rat MYO(Myoglobin) ELISA Kit, 96T

ELK2608-96T, Rat MYO(Myoglobin) ELISA Kit, 96T

ELK2608-48T, Rat MYO(Myoglobin) ELISA Kit, 48T

2.142,00 RON

Rat MYO(Myoglobin) ELISA Kit

SKU
ELK2608-48T

Alternative Names: PVALB; MB

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.238 ng/mL

Standard: 40 ng/mL

Detection range: 0.63-40 ng/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids.

Assay length: 3.5h

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

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Description

Alternative Names: PVALB; MB

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.238 ng/mL

Standard: 40 ng/mL

Detection range: 0.63-40 ng/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids.

Assay length: 3.5h

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