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ELK4016-48T, Human RNASEH(Ribonuclease H) ELISA Kit, 48T

2.142,00 RON

Human RNASEH(Ribonuclease H) ELISA Kit

SKU
ELK4016-48T

Alternative Names: Rnase-H; RNASEH1; RNH1; Ribonuclease H type II

Species: Human

Assay Type: Sandwich

Sensitivity: 0.052 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

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

Assay length: 3.5h

Research Area: Enzyme & Kinase;Infection immunity;Developmental science;

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

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Description

Alternative Names: Rnase-H; RNASEH1; RNH1; Ribonuclease H type II

Species: Human

Assay Type: Sandwich

Sensitivity: 0.052 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

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

Assay length: 3.5h

Research Area: Enzyme & Kinase;Infection immunity;Developmental science;

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