ELK3499-96T, Human CPR(Cytochrome P450 Reductase) ELISA Kit, 96T

ELK3499-96T, Human CPR(Cytochrome P450 Reductase) ELISA Kit, 96T

ELK3500-96T, Human FUR(Furin) ELISA Kit, 96T

ELK3500-96T, Human FUR(Furin) ELISA Kit, 96T

ELK3500-48T, Human FUR(Furin) ELISA Kit, 48T

2.142,00 RON

Human FUR(Furin) ELISA Kit

SKU
ELK3500-48T

Alternative Names: PACE; PCSK3; SPC1; Paired Basic Amino Acid Cleaving Enzyme; Dibasic-processing enzyme

Species: Human

Assay Type: Sandwich

Sensitivity: 0.061 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: Enzyme & Kinase;Metabolic pathway;Hematology;

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

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Description

Alternative Names: PACE; PCSK3; SPC1; Paired Basic Amino Acid Cleaving Enzyme; Dibasic-processing enzyme

Species: Human

Assay Type: Sandwich

Sensitivity: 0.061 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: Enzyme & Kinase;Metabolic pathway;Hematology;

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