ELK4051-48T, Human CPM(Carboxypeptidase M) ELISA Kit, 48T

ELK4051-48T, Human CPM(Carboxypeptidase M) ELISA Kit, 48T

ELK4052-48T, Human CUBN(Cubilin) ELISA Kit, 48T

ELK4052-48T, Human CUBN(Cubilin) ELISA Kit, 48T

ELK4051-96T, Human CPM(Carboxypeptidase M) ELISA Kit, 96T

2.963,10 RON

Human CPM(Carboxypeptidase M) ELISA Kit

SKU
ELK4051-96T

Alternative Names: Carboxypeptidase M; CBPM_HUMAN; CPM; Renal carboxypeptidase; Urinary carboxypeptidase B

Species: Human

Assay Type: Sandwich

Sensitivity: 28 pg/mL

Standard: 5000 pg/mL

Detection range: 78.13-5000 pg/mL

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

Assay length: 3.5h

Research Area: Enzyme & Kinase;Tumor immunity;Infection immunity;Hormone 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 CPM. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CPM. 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 CPM, 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 CPM in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Carboxypeptidase M; CBPM_HUMAN; CPM; Renal carboxypeptidase; Urinary carboxypeptidase B

Species: Human

Assay Type: Sandwich

Sensitivity: 28 pg/mL

Standard: 5000 pg/mL

Detection range: 78.13-5000 pg/mL

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

Assay length: 3.5h

Research Area: Enzyme & Kinase;Tumor immunity;Infection immunity;Hormone 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 CPM. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CPM. 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 CPM, 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 CPM in the samples is then determined by comparing the OD of the samples to the standard curve.