ELK2049-48T, Human GRP(Gla Rich Protein) ELISA Kit, 48T

ELK2049-48T, Human GRP(Gla Rich Protein) ELISA Kit, 48T

ELK2050-48T, Human PROZ(Protein Z) ELISA Kit, 48T

ELK2050-48T, Human PROZ(Protein Z) ELISA Kit, 48T

ELK2049-96T, Human GRP(Gla Rich Protein) ELISA Kit, 96T

2.963,10 RON

Human GRP(Gla Rich Protein) ELISA Kit

SKU
ELK2049-96T

Alternative Names: GRP

Species: Human

Assay Type: Sandwich

Sensitivity: 1.17 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

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

Assay length: 3.5h

Research Area: Developmental science;Bone metabolism;

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

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Description

Alternative Names: GRP

Species: Human

Assay Type: Sandwich

Sensitivity: 1.17 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

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

Assay length: 3.5h

Research Area: Developmental science;Bone metabolism;

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