ELK9585-48T, Human ATXN2(Ataxin 2) ELISA Kit, 48T

ELK9585-48T, Human ATXN2(Ataxin 2) ELISA Kit, 48T

ELK9586-48T, Human Collagenase Ⅰ ELISA Kit, 48T

ELK9586-48T, Human Collagenase Ⅰ ELISA Kit, 48T

ELK9585-96T, Human ATXN2(Ataxin 2) ELISA Kit, 96T

2.963,10 RON

Human ATXN2(Ataxin 2) ELISA Kit

SKU
ELK9585-96T

Alternative Names: ASL13; ATX2; SCA2; TNRC13

Species: Human

Assay Type: Sandwich

Sensitivity: 0.47 ng/mL

Standard: 50 ng/mL

Detection range: 0.78-50 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 3.5h

Research Area: Epigenetics and Nuclear Signaling;Neuroscience;Cell Biology

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 ATXN2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ATXN2. 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 ATXN2, 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 ATXN2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ASL13; ATX2; SCA2; TNRC13

Species: Human

Assay Type: Sandwich

Sensitivity: 0.47 ng/mL

Standard: 50 ng/mL

Detection range: 0.78-50 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 3.5h

Research Area: Epigenetics and Nuclear Signaling;Neuroscience;Cell Biology

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 ATXN2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ATXN2. 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 ATXN2, 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 ATXN2 in the samples is then determined by comparing the OD of the samples to the standard curve.