ELK3522-96T, Human HNRPU(Heterogeneous Nuclear Ribonucleoprotein U) ELISA Kit, 96T

ELK3522-96T, Human HNRPU(Heterogeneous Nuclear Ribonucleoprotein U) ELISA Kit, 96T

ELK3523-96T, Human PFDN1(Prefoldin Subunit 1) ELISA Kit, 96T

ELK3523-96T, Human PFDN1(Prefoldin Subunit 1) ELISA Kit, 96T

ELK3523-48T, Human PFDN1(Prefoldin Subunit 1) ELISA Kit, 48T

2.142,00 RON

Human PFDN1(Prefoldin Subunit 1) ELISA Kit

SKU
ELK3523-48T

Alternative Names: PDF; PFD1

Species: Human

Assay Type: Sandwich

Sensitivity: 0.112 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates, cell Lysates and other biological fluids.

Assay length: 3.5h

Research Area: Infection immunity;

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 PFDN1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PFDN1. 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 PFDN1, 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 PFDN1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: PDF; PFD1

Species: Human

Assay Type: Sandwich

Sensitivity: 0.112 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates, cell Lysates and other biological fluids.

Assay length: 3.5h

Research Area: Infection immunity;

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 PFDN1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PFDN1. 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 PFDN1, 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 PFDN1 in the samples is then determined by comparing the OD of the samples to the standard curve.