ELK7188-48T, Rat MYCBP(C-Myc Binding Protein) ELISA Kit, 48T

ELK7188-48T, Rat MYCBP(C-Myc Binding Protein) ELISA Kit, 48T

ELK7189-48T, Mouse MIA1(Melanoma Inhibitory Activity Protein 1) ELISA Kit, 48T

ELK7189-48T, Mouse MIA1(Melanoma Inhibitory Activity Protein 1) ELISA Kit, 48T

ELK7188-96T, Rat MYCBP(C-Myc Binding Protein) ELISA Kit, 96T

2.963,10 RON

Rat MYCBP(C-Myc Binding Protein) ELISA Kit

SKU
ELK7188-96T

Alternative Names: AMY-1; Associate Of Myc-1

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 and other biological fluids.

Assay length: 3.5h

Research Area: Tumor immunity;

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

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Description

Alternative Names: AMY-1; Associate Of Myc-1

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 and other biological fluids.

Assay length: 3.5h

Research Area: Tumor immunity;

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