ELK8112-96T, Cattle CL43(Collectin Of 43kDa) ELISA Kit, 96T

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ELK8113-96T, Rat MYBL1(V-Myb Myeloblastosis Viral Oncogene Homolog Like Protein 1) ELISA Kit, 96T

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ELK8113-48T, Rat MYBL1(V-Myb Myeloblastosis Viral Oncogene Homolog Like Protein 1) ELISA Kit, 48T

2.142,00 RON

Rat MYBL1(V-Myb Myeloblastosis Viral Oncogene Homolog Like Protein 1) ELISA Kit

SKU
ELK8113-48T

Alternative Names: AMYB; A-myb; MYBA; Myb-related protein A

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.057 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Tissue homogenates, cell lysates 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 MYBL1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MYBL1. 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 MYBL1, 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 MYBL1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: AMYB; A-myb; MYBA; Myb-related protein A

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.057 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Tissue homogenates, cell lysates 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 MYBL1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MYBL1. 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 MYBL1, 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 MYBL1 in the samples is then determined by comparing the OD of the samples to the standard curve.