ELK9351-96T, Human sIL30(Soluble Interleukin 30) ELISA Kit, 96T

ELK9351-96T, Human sIL30(Soluble Interleukin 30) ELISA Kit, 96T

ELK9352-96T, Rat γH2AX(gamma H2A.X) ELISA Kit, 96T

ELK9352-96T, Rat γH2AX(gamma H2A.X) ELISA Kit, 96T

ELK9352-48T, Rat γH2AX(gamma H2A.X) ELISA Kit, 48T

2.142,00 RON

Rat γH2AX(gamma H2A.X) ELISA Kit

SKU
ELK9352-48T

Alternative Names: gamma H2A.X; γH2AX; Phospho-H2AX-S139

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.059 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: tissue homogenates, cell lysates, cell culture supernates 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 Rat γH2AX. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat γH2AX. 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 Rat γH2AX, 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 Rat γH2AX in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: gamma H2A.X; γH2AX; Phospho-H2AX-S139

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.059 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: tissue homogenates, cell lysates, cell culture supernates 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 Rat γH2AX. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat γH2AX. 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 Rat γH2AX, 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 Rat γH2AX in the samples is then determined by comparing the OD of the samples to the standard curve.