ELK3909-48T, Human PLXNB1(Plexin B1) ELISA Kit, 48T

ELK3909-48T, Human PLXNB1(Plexin B1) ELISA Kit, 48T

ELK3910-48T, Human ESAM(Endothelial Cell Adhesion Molecule) ELISA Kit, 48T

ELK3910-48T, Human ESAM(Endothelial Cell Adhesion Molecule) ELISA Kit, 48T

ELK3909-96T, Human PLXNB1(Plexin B1) ELISA Kit, 96T

2.963,10 RON

Human PLXNB1(Plexin B1) ELISA Kit

SKU
ELK3909-96T

Alternative Names: PLXN5; SEP; Semaphorin receptor SEP

Species: Human

Assay Type: Sandwich

Sensitivity: 0.62 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: tissue homogenates, cell lysates 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 Human PLXNB1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PLXNB1. 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 PLXNB1, 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 PLXNB1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: PLXN5; SEP; Semaphorin receptor SEP

Species: Human

Assay Type: Sandwich

Sensitivity: 0.62 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: tissue homogenates, cell lysates 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 Human PLXNB1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PLXNB1. 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 PLXNB1, 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 PLXNB1 in the samples is then determined by comparing the OD of the samples to the standard curve.