Title of article :
Detection of chromogranin A in the adrenal gland extracts of different animal species by an enzyme-linked immunosorbent assay using Thomsen–Friedenreich antigen-specific Amaranthus caudatus lectin
Author/Authors :
Akiyoshi، نويسنده , , Hideo and Sugii، نويسنده , , Shunji and Nahid، نويسنده , , Md. A. and Sone، نويسنده , , Katsuhito and Tanaka، نويسنده , , Toshiyuki and Zheng، نويسنده , , Cao and Yijyun، نويسنده , , Li and Aoki، نويسنده , , Mica and Takenaka، نويسنده , , Shigeo and Shimada، نويسنده , , Terumasa and Shimizu، نويسنده , , Junichiro and Kiyomiya، نويسنده , , Ken-ichi and Ohashi، نويسنده , , Fumihito، نويسنده ,
Pages :
4
From page :
255
To page :
258
Abstract :
The reactivity of different lectins with crude chromogranin A (CgA) obtained from different animals, namely, cow, horse, dog, pig, and dolphin, was examined to identify lectin(s) that would be useful as coating reagent(s) in a sandwich enzyme-linked immunosorbent assay (ELISA). Of the different lectins studied, the Amaranthus caudatus lectin (ACA), which is specific for the Thomsen–Friedenreich (T)-antigen (Galβ1-3GalNAc), was found to react with the CgA from different animals by western blotting. Purified rabbit anti-bovine CgA antibody was also found to cross-react with the crude CgA preparations. On the basis of these findings, a sandwich ELISA was developed with ACA as the coating reagent and anti-bovine CgA antibody as the probing antibody. Using this method, concentration-dependent curves ranging from 0.003 μg/mL to 25 μg/mL and from 0.02 μg/mL to 25 μg/mL were obtained for bovine CgA and canine CgA, respectively. Similarly, concentration-dependent curves were obtained for the equine, swine, and dolphin crude CgA extracts. Thus, ACA is concluded to be a valuable reagent for CgA detection in crude extracts from different animal species, and for CgA isolation/purification.
Keywords :
Chromogranin A , Amaranthus caudatus , Lectin
Journal title :
Astroparticle Physics
Record number :
2061379
Link To Document :
بازگشت