Mouse Zymogen granule membrane protein 16, ZG16 ELISA Kit
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!
Synonyms
Zymogen granule membrane protein 16,Zymogen granule protein 16,hZG16,Secretory lectin ZG16,ZG16,ZG16B,secretory lectin ZG16; JCLN; JCLN1; ZG16A; jacalin-like lectin domain containing; zymogen granule membrane protein 16; zymogen granule protein 16 homolog; zymogen granule protein 16,
Search name
Mouse Zymogen granule membrane protein 16 ELISA KIT ,Mouse Zymogen granule protein 16 ELISA KIT ,Mouse hZG16 ELISA KIT ,Mouse Secretory lectin ZG16 ELISA KIT ,Mouse ZG16 ELISA KIT ,Mouse ZG16B ELISA KIT ,Mouse secretory lectin ZG16 ELISA KIT ,Mouse JCLN ELISA KIT ,Mouse JCLN1 ELISA KIT ,Mouse ZG16A ELISA KIT ,Mouse jacalin-like lectin domain containing ELISA KIT ,Mouse zymogen granule membrane protein 16 ELISA KIT ,Mouse zymogen granule protein 16 homolog ELISA KIT ,Mouse zymogen granule protein 16 ELISA KIT
Intended use
This immunoassay kit allows for the in vitro quantitative determination of Mouse zymogen granule membrane protein 16,hZG16 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 hZG16. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for hZG16 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 hZG16, 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 hZG16 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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