Mouse Hepatocellular carcinoma- associated protein TD26, TD26 ELISA Kit
96 Tests
Operating instruction

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

Synonyms
Hepatocellular carcinoma-associated protein TD26, C19orf80,hepatocellular carcinoma-associated protein TD26; ANGPTL8; PRO1185; PVPA599; RIFL;
TD26; hepatocellular carcinoma-associated gene TD26; lipasin; chromosome 19 open reading frame 80

Search name
Mouse Hepatocellular carcinoma-associated protein TD26, TD26 ELISA Kit, Mouse TD26 ELISA Kit, Mouse C19orf80 ELISA Kit, Mouse ANGPTL8
ELISA Kit, Mouse PRO1185 ELISA Kit, Mouse PVPA599 ELISA Kit, Mouse RIFL ELISA Kit, Mouse hepatocellular carcinoma-associated gene TD26
ELISA Kit, Mouse lipasin; chromosome 19 open reading frame 80 ELISA Kit

Intended use
This immunoassay kit allows for the in vitro quantitative determination of mouse Hepatocellular carcinoma-associated protein TD26
homolog 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 Hepatocellular carcinoma-associated protein
TD26 homolog. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody
preparation specific for Hepatocellular carcinoma-associated protein TD26 homolog 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
Hepatocellular carcinoma-associated protein TD26 homolog, 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 Hepatocellular carcinoma-associated protein
TD26 homolog in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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