ELK7467-48T, Human H2AFX(H2A Histone Family, Member X) ELISA Kit, 48T

ELK7467-48T, Human H2AFX(H2A Histone Family, Member X) ELISA Kit, 48T

ELK7468-48T, Rat URAT1(Urate Transporter 1) ELISA Kit, 48T

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ELK7467-96T, Human H2AFX(H2A Histone Family, Member X) ELISA Kit, 96T

2.963,10 RON

Human H2AFX(H2A Histone Family, Member X) ELISA Kit

SKU
ELK7467-96T

Alternative Names: H2AX

Species: Human

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 Human H2AFX. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human H2AFX. 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 H2AFX, 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 H2AFX in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: H2AX

Species: Human

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 Human H2AFX. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human H2AFX. 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 H2AFX, 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 H2AFX in the samples is then determined by comparing the OD of the samples to the standard curve.