ELK6394-96T, Human PRSS23(Protease, Serine 23) ELISA Kit, 96T

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ELK6395-96T, Rat NID2(Nidogen 2) ELISA Kit, 96T

ELK6395-96T, Rat NID2(Nidogen 2) ELISA Kit, 96T

ELK6395-48T, Rat NID2(Nidogen 2) ELISA Kit, 48T

2.142,00 RON

Rat NID2(Nidogen 2) ELISA Kit

SKU
ELK6395-48T

Alternative Names: Osteonidogen

Species: Rat

Assay Type: Sandwich

Sensitivity: 3.2 ng/mL

Standard: 500 ng/mL

Detection range: 7.82-500 ng/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 3.5h

Research Area: Metabolic pathway;

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 NID2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NID2. 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 NID2, 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 NID2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Osteonidogen

Species: Rat

Assay Type: Sandwich

Sensitivity: 3.2 ng/mL

Standard: 500 ng/mL

Detection range: 7.82-500 ng/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 3.5h

Research Area: Metabolic pathway;

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 NID2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NID2. 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 NID2, 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 NID2 in the samples is then determined by comparing the OD of the samples to the standard curve.