ELK8663-48T, Rat MAU(Microalbuminuria) ELISA Kit, 48T

ELK8663-48T, Rat MAU(Microalbuminuria) ELISA Kit, 48T

ELK8664-48T, Rat TBA(Total Bile Acid) ELISA Kit, 48T

ELK8664-48T, Rat TBA(Total Bile Acid) ELISA Kit, 48T

ELK8663-96T, Rat MAU(Microalbuminuria) ELISA Kit, 96T

2.963,10 RON

Rat MAU(Microalbuminuria) ELISA Kit

SKU
ELK8663-96T

Alternative Names: MAU; Microalbuminuria

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.48 µg/mL

Standard: 100 µg/mL

Detection range: 1.57-100 µg/mL

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

Assay length: 3.5h

Research Area: Diabetes

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

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Description

Alternative Names: MAU; Microalbuminuria

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.48 µg/mL

Standard: 100 µg/mL

Detection range: 1.57-100 µg/mL

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

Assay length: 3.5h

Research Area: Diabetes

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