Mouse Molybdenum cofactor sulfurase, MOCOS ELISA KIT

96 Tests

Operating instruction

FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!

Synonyms

2.8.1.9,Molybdenum cofactor sulfurase,MCS,MOS,MoCo sulfurase,hMCS,Molybdenum cofactor sulfurtransferase,,MCSU,SMCP,MCS,HSMCSGEN1,MCSP,mitochondrial capsule selenoprotein,sperm mitochondrial-associated cysteine-rich protein,sperm mitochondria-associated cysteine-rich protein

Search name

Mouse 2.8.1.9 ELISA KIT ,Mouse Molybdenum cofactor sulfurase ELISA KIT ,Mouse MCS ELISA KIT ,Mouse MOS ELISA KIT ,Mouse MoCo sulfurase ELISA KIT ,Mouse hMCS ELISA KIT ,Mouse Molybdenum cofactor sulfurtransferase ELISA KIT ,Mouse  ELISA KIT ,Mouse MCSU ELISA KIT ,Mouse SMCP ELISA KIT ,Mouse MCS ELISA KIT ,Mouse HSMCSGEN1 ELISA KIT ,Mouse MCSP ELISA KIT ,Mouse mitochondrial capsule selenoprotein ELISA KIT ,Mouse sperm mitochondrial-associated cysteine-rich protein ELISA KIT ,Mouse sperm mitochondria-associated cysteine-rich protein ELISA KIT

Intended use

This immunoassay kit allows for the in vitro quantitative determination of Mouse molybdenum cofactor sulfurase,MCS concentrations in serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.

Test principle

The microtiter plate provided in this kit has been pre-coated with an antibody specific to MCS. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for MCS and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain MCS, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of MCS in the samples is then determined by comparing the O.D. of the samples to the standard curve.