Human 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
Human 2.8.1.9 ELISA KIT ,Human Molybdenum cofactor sulfurase ELISA KIT ,Human MCS ELISA KIT ,Human MOS ELISA KIT ,Human MoCo sulfurase ELISA KIT ,Human hMCS ELISA KIT ,Human Molybdenum cofactor sulfurtransferase ELISA KIT ,Human ELISA KIT ,Human MCSU ELISA KIT ,Human SMCP ELISA KIT ,Human MCS ELISA KIT ,Human HSMCSGEN1 ELISA KIT ,Human MCSP ELISA KIT ,Human mitochondrial capsule selenoprotein ELISA KIT ,Human sperm mitochondrial-associated cysteine-rich protein ELISA KIT ,Human sperm mitochondria-associated cysteine-rich protein ELISA KIT
Intended use
This immunoassay kit allows for the in vitro quantitative determination of human 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.
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