ELK8623-96T, Human CTXI(Cross-linked Carboxy-terminal telopeptide of type Ⅰ collagen) ELISA Kit, 96T

ELK8623-96T, Human CTXI(Cross-linked Carboxy-terminal telopeptide of type Ⅰ collagen) ELISA Kit, 96T

ELK8624-96T, Human Transcriptional regulator ATRX (ATRX) ELISA Kit, 96T

ELK8624-96T, Human Transcriptional regulator ATRX (ATRX) ELISA Kit, 96T

ELK8624-48T, Human Transcriptional regulator ATRX (ATRX) ELISA Kit, 48T

2.142,00 RON

Human Transcriptional regulator ATRX (ATRX) ELISA Kit

SKU
ELK8624-48T

Alternative Names: ATRX

Species: Human

Assay Type: Sandwich

Sensitivity: 0.082 ng/mL

Standard: 20 ng/mL

Detection range: 0.31-20 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Glioma

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

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Description

Alternative Names: ATRX

Species: Human

Assay Type: Sandwich

Sensitivity: 0.082 ng/mL

Standard: 20 ng/mL

Detection range: 0.31-20 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Glioma

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