ELISA/assay

B2-Microglobulin ELISA

B3M31-K01

1 x 96 well

300 USD

B2-Microglobulin ELISA

The principle of the following enzyme immunoassay test follows the typical competitive binding scenario. Competition occurs between an unlabelled antigen (present in standards, controls and patient samples) and an enzyme-labelled antigen (conjugate) for a limited number of antibody binding sites on the microplate. The washing and decanting procedures remove unbound materials. After the washing step, the enzyme substrate is added. The enzymatic reaction is terminated by addition of the stopping solution. The absorbance is measured on a microtiter plate reader. The intensity of the colour formed is inversely proportional to the concentration of β2 -M in the sample. A set of standards is used to plot a standard curve from which the amount of β2-M in patient samples and controls can be directly read.

ELISA

Assay Kit

Endocrine

1 x 96 well

B2-microglobulin

B2-microglobulin

0.1 mg/L

0.2–10 mg/L

20 μL

Serum

1.5 hours

Human

RUO

wet

2-8C

300 USD