Mouse Uteroglobin, SCGB1A1 ELISA KIT
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!
Synonyms
Scgb1a1,CC10; CC16; CCPBP; CCSP; UGB; UP-1; UP1; Uteroglobin,Urinary protein 1,Secretoglobin family 1A member 1,Clara cell phospholipid-binding protein,blastokinin; clara cell phospholipid-binding protein; clara cells 10 kDa secretory protein; urinary protein 1; urine protein 1
Search name
Mouse Scgb1a1 ELISA KIT ,Mouse CC10 ELISA KIT ,Mouse CC16 ELISA KIT ,Mouse CCPBP ELISA KIT ,Mouse CCSP ELISA KIT ,Mouse UGB ELISA KIT ,Mouse UP-1 ELISA KIT ,Mouse UP1 ELISA KIT ,Mouse Uteroglobin ELISA KIT ,Mouse Urinary protein 1 ELISA KIT ,Mouse Secretoglobin family 1A member 1 ELISA KIT ,Mouse Clara cell phospholipid-binding protein ELISA KIT ,Mouse blastokinin ELISA KIT ,Mouse clara cell phospholipid-binding protein ELISA KIT ,Mouse clara cells 10 kDa secretory protein ELISA KIT ,Mouse urinary protein 1 ELISA KIT ,Mouse urine protein 1 ELISA KIT
Intended use
This immunoassay kit allows for the in vitro quantitative determination of mouse Uteroglobin concentrations in serum, Plasma, Urine, 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 Uteroglobin. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for Uteroglobin 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 Uteroglobin, 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 Uteroglobin in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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