©1996-2021. All Rights Reserved. Online Journal of Veterinary Research. You may not store these pages in any form except for your own personal use. All other usage or distribution is illegal under international copyright treaties. Permission to use any of these pages in any other way besides the before mentioned must be gained in writing from the publisher. This article is exclusively copyrighted in its entirety to OJVR. This article may be copied once but may not be, reproduced or re-transmitted without the express permission of the editors. This journal satisfies the refereeing requirements (DEST) for the Higher Education Research Data Collection (Australia). Linking: To link to this page or any pages linking to this page you must link directly to this page only here rather than put up your own page.
Online Journal of Veterinary Research©
Volume 23 (10):999-1004, 2019.
DNA clone encoding 34.9 kDa Carboxy terminal proline glutamic acid
protein of Mycobacterium avium paratuberculosis in E. Coli.
Deb R, Goswami PP, Prasad NS
Gene Expression Lab, Department of Animal Biotechnology, Indian Veterinary Research Institute, Izatnagar, India
Deb R, Goswami PP, Prasad NS., DNA clone encoding 34.9 kDa Carboxy terminal proline glutamic acid protein of Mycobacterium avium paratuberculosis in E. Coli., Onl J Vet Res., 23 (10):999-1006, 2019. Mycobacterium avium ssp. Paratuberculosis is the causative agent of Johne’s disease in animals. A PPE (Proline Proline Glutamic acid rich) antigen encoding 34.9 kDa hypothetical protein of M.avium subsp. Paratuberculosis was cloned and sequenced. Sequence analysis revealed that no other published sequences having significant homology with that PPE gene, suggesting that PPE 34.9- kDa could be used as a diagnostic antigen.
Key Words PPE, 34.9 kDa, Mycobacterium avium ssp. Paratuberculosis, FJ032182.