Bovine Prolactin-inducible protein, PIP ELISA Kit
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!
Synonyms
Prolactin-inducible protein,gp17,Secretory actin-binding protein,SABP,Gross cystic disease fluid protein 15,GCDFP-15,Prolactin-induced protein, PIP,prolactin-inducible protein; GCDFP-15; GCDFP15; GPIP4; SABP; gross cystic disease fluid protein 15; secretory actin-binding protein; prolactin-induced protein
Search name
Bovine Prolactin-inducible protein ELISA KIT ,Bovine gp17 ELISA KIT ,Bovine Secretory actin-binding protein ELISA KIT ,Bovine SABP ELISA KIT ,Bovine Gross cystic disease fluid protein 15 ELISA KIT ,Bovine GCDFP-15 ELISA KIT ,Bovine Prolactin-induced protein ELISA KIT ,Bovine PIP ELISA KIT ,Bovine prolactin-inducible protein ELISA KIT ,Bovine GCDFP-15 ELISA KIT ,Bovine GCDFP15 ELISA KIT ,Bovine GPIP4 ELISA KIT ,Bovine SABP ELISA KIT ,Bovine gross cystic disease fluid protein 15 ELISA KIT ,Bovine secretory actin-binding protein ELISA KIT ,Bovine prolactin-induced protein ELISA KIT
Intended use
This immunoassay kit allows for the in vitro quantitative determination of Bovine prolactin-inducible protein,PIP 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 PIP. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for PIP 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 PIP, 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 PIP in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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